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1. Vorburger SA, Xing Y, Hunt KK, Lakin GE, Benjamin RS, Feig BW, Pisters PW, Ballo MT, Chen L, Trent J 3rd, Burgess M, Patel S, Pollock RE, Cormier JN: Angiosarcoma of the breast. Cancer; 2005 Dec 15;104(12):2682-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the breast.
  • BACKGROUND: Angiosarcoma of the breast is a rare entity.
  • METHODS: Clinical and pathologic factors were analyzed in all patients with angiosarcoma of the breast treated between 1990 and 2003.
  • RESULTS: Fifty-five women with angiosarcoma of the breast were identified.
  • For the 32 patients with primary angiosarcoma of the breast 5-year OS was 59%.
  • These patients with radiation therapy-associated angiosarcoma were on average 30 years older and less likely to present with distant metastatic disease than patients presenting with radiation-naive angiosarcoma of the breast.
  • CONCLUSIONS: In this series of 55 patients with angiosarcoma of the breast, radiation therapy-naive angiosarcomas occurred in younger patients, but they behaved similarly to radiation therapy-associated angiosarcomas.
  • [MeSH-major] Breast Neoplasms / mortality. Breast Neoplasms / therapy. Hemangiosarcoma / mortality. Hemangiosarcoma / therapy. Mastectomy / methods
  • [MeSH-minor] Adult. Biopsy, Needle. Chemotherapy, Adjuvant. Cohort Studies. Combined Modality Therapy. Confidence Intervals. Disease-Free Survival. Female. Humans. Immunohistochemistry. Middle Aged. Neoplasm Staging. Probability. Prognosis. Proportional Hazards Models. Radiotherapy, Adjuvant. Retrospective Studies. Risk Assessment. Survival Analysis

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  • [Copyright] Copyright 2005 American Cancer Society.
  • (PMID = 16288486.001).
  • [ISSN] 0008-543X
  • [Journal-full-title] Cancer
  • [ISO-abbreviation] Cancer
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
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2. Hsu CW, Lin CH, Yang TL, Chang HT: Splenic inflammatory pseudotumor mimicking angiosarcoma. World J Gastroenterol; 2008 Nov 7;14(41):6421-4
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  • [Title] Splenic inflammatory pseudotumor mimicking angiosarcoma.
  • A case of a 32-year-old man with a splenic inflammatory pseudotumor (IPT) mimicking splenic angiosarcoma is described.
  • The tumor was highly suspected of being splenic angiosarcoma based on radiological findings preoperatively.
  • Splenic IPT and angiosarcoma are rare and often pose diagnostic difficulties because the clinical and radiological findings are obscure.
  • [MeSH-major] Granuloma, Plasma Cell / pathology. Hemangiosarcoma / pathology. Splenic Diseases / pathology. Splenic Neoplasms / pathology
  • [MeSH-minor] Adult. Diagnosis, Differential. Humans. Magnetic Resonance Imaging. Male. Splenectomy. Tomography, X-Ray Computed. Treatment Outcome. Ultrasonography

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  • [Cites] J Natl Med Assoc. 2000 Mar;92(3):143-6 [10745645.001]
  • [Cites] Surg Today. 2000;30(10):942-6 [11059739.001]
  • [Cites] Arch Pathol Lab Med. 2001 Mar;125(3):379-85 [11231487.001]
  • [Cites] Virchows Arch. 2001 Jun;438(6):629-31 [11469697.001]
  • [Cites] Ann Hematol. 2005 Sep;84(9):619-20 [15841410.001]
  • [Cites] Radiat Med. 1998 Jan-Feb;16(1):47-50 [9568633.001]
  • [Cites] Hepatogastroenterology. 1998 Sep-Oct;45(23):1887-91 [9840170.001]
  • [Cites] J Chin Med Assoc. 2004 Oct;67(10):533-6 [15648289.001]
  • [Cites] Radiology. 2005 Apr;235(1):106-15 [15749977.001]
  • [Cites] Acta Radiol. 1994 Sep;35(5):455-8 [8086253.001]
  • (PMID = 19009664.001).
  • [ISSN] 1007-9327
  • [Journal-full-title] World journal of gastroenterology
  • [ISO-abbreviation] World J. Gastroenterol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] China
  • [Other-IDs] NLM/ PMC2766130
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3. Kar A, Mukhopadhyay D, Das SS, Swain NN, Das BM, Nayak M, Rath J, Satpathy S: Cytodiagnosis of angiosarcoma of breast. Indian J Pathol Microbiol; 2008 Jul-Sep;51(3):427-9
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  • [Title] Cytodiagnosis of angiosarcoma of breast.
  • The case was diagnosed by preoperative cytology as angiosarcoma of breast, after which, she underwent modified radical mastectomy.
  • Angiosarcoma of breast is uncommon with extremely bad prognosis.
  • [MeSH-major] Breast Neoplasms / diagnosis. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Cytodiagnosis. Female. Humans. Mastectomy

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  • (PMID = 18723981.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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4. Rodríguez-Bujaldón A, Vázquez-Bayo MC, Galán-Gutiérrez M, Jiménez-Puya R, Vélez García-Nieto A, Moreno-Giménez JC, Vidal-Jiménez A, Barroso-Casamitjana E: [Angiosarcoma in chronic lymphedema]. Actas Dermosifiliogr; 2006 Oct;97(8):525-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Angiosarcoma in chronic lymphedema].
  • [Transliterated title] Angiosarcoma sobre linfedema crónico.
  • Angiosarcoma that develops on a limb with chronic lymphedema is called Stewart-Treves syndrome.
  • The first corresponds to a typical syndrome of Stewart-Treves in an 83-year-old woman who was diagnosed of angiosarcoma in a chronic lymphedema territory secondary to mastectomy and radiotherapy due to breast cancer.
  • The second case is much rarer, since it is a case of diffuse angiosarcoma of the leg in a 42-year-old man with a history of lymphedema.
  • [MeSH-major] Hemangiosarcoma / etiology. Lymphedema / complications
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Antibiotics, Antineoplastic / administration & dosage. Antibiotics, Antineoplastic / therapeutic use. Antineoplastic Agents, Alkylating / administration & dosage. Antineoplastic Agents, Alkylating / therapeutic use. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Arm. Doxorubicin / administration & dosage. Doxorubicin / therapeutic use. Female. Humans. Ifosfamide / administration & dosage. Ifosfamide / therapeutic use. Immunohistochemistry. Leg. Male. Skin / pathology. Skin Neoplasms / diagnosis. Skin Neoplasms / drug therapy. Skin Neoplasms / etiology. Skin Neoplasms / pathology. Skin Neoplasms / radiotherapy. Treatment Outcome

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  • (PMID = 17067532.001).
  • [ISSN] 0001-7310
  • [Journal-full-title] Actas dermo-sifiliográficas
  • [ISO-abbreviation] Actas Dermosifiliogr
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
  • [Chemical-registry-number] 0 / Antibiotics, Antineoplastic; 0 / Antineoplastic Agents, Alkylating; 80168379AG / Doxorubicin; UM20QQM95Y / Ifosfamide
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5. Bouhaouala MH, Charfi MR, Fajraoui N, Bouaziz N, Boukhris A, Kilani T: [Primary pulmonary angiosarcoma]. Rev Pneumol Clin; 2005 Apr;61(2):115-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Primary pulmonary angiosarcoma].
  • Pulmonary angiosarcoma is an uncommon vascular and usually secondary tumor.
  • Only a few primary cases of pulmonary angiosarcoma have been described.
  • We report a case of primary pulmonary angiosarcoma in an adult man who presented with hemoptysis.
  • Pulmonary angiosarcoma was diagnosed on histological and immuno-histochemical studies of the operative specimen.
  • This observation is added to the other rare cases published of primitive pulmonary angiosarcoma.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Lung Neoplasms / diagnosis

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  • (PMID = 16012366.001).
  • [ISSN] 0761-8417
  • [Journal-full-title] Revue de pneumologie clinique
  • [ISO-abbreviation] Rev Pneumol Clin
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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6. Hsu JT, Lin CY, Wu TJ, Chen HM, Hwang TL, Jan YY: Splenic angiosarcoma metastasis to small bowel presented with gastrointestinal bleeding. World J Gastroenterol; 2005 Nov 7;11(41):6560-2
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  • [Title] Splenic angiosarcoma metastasis to small bowel presented with gastrointestinal bleeding.
  • Primary splenic angiosarcoma is a very rare, aggressive neoplasm with a high metastatic rate and dismal prognosis.
  • Splenic angiosarcoma with bleeding gastrointestinal metastases is extremely rare.
  • This study reported a 44-year-old male patient with splenic angiosarcoma with sustained repeated gastrointestinal bleeding due to small bowel metastases.
  • [MeSH-major] Gastrointestinal Hemorrhage / etiology. Hemangiosarcoma / secondary. Intestinal Neoplasms / secondary. Splenic Neoplasms / pathology
  • [MeSH-minor] Adult. Humans. Male

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  • (PMID = 16425436.001).
  • [ISSN] 1007-9327
  • [Journal-full-title] World journal of gastroenterology
  • [ISO-abbreviation] World J. Gastroenterol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] China
  • [Other-IDs] NLM/ PMC4355806
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7. Li Q, Wang J, Sun Y, Cui Y, Hao X: Hepatic angiosarcoma arising in an adult mesenchymal hamartoma. Int Semin Surg Oncol; 2007;4:3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Hepatic angiosarcoma arising in an adult mesenchymal hamartoma.
  • The histogenesis of the hepatic sarcoma and its association with hamartoma is not well understood.
  • We hereby present a Chinese patient with hepatic angiosarcoma arising from an adult mesenchymal hamartoma of liver.
  • Now she was admitted to our hospital with some unusual features: (a) this patient was diagnosed in mid-twenties, (b) the tumor occupied the whole liver and most importantly (c) the hepatic angiosarcoma appeared 8 years after the diagnosis of hamartoma.
  • Based on this case and some reports, hepatic hamartoma may develop to hepatic angiosarcoma.

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  • [Cites] Mod Pathol. 1994 May;7(4):490-3 [8066077.001]
  • [Cites] Am J Surg Pathol. 1997 Oct;21(10):1248-54 [9331300.001]
  • [Cites] Radiographics. 1994 Jan;14(1):153-66; quiz 167-8 [8128048.001]
  • [Cites] Am J Ind Med. 1981;2(1):43-50 [6891179.001]
  • [Cites] Pediatr Pathol. 1983 Jul-Sep;1(3):245-67 [6687279.001]
  • [Cites] AJR Am J Roentgenol. 1986 May;146(5):997-1004 [3008544.001]
  • [Cites] Pediatr Dev Pathol. 2001 Sep-Oct;4(5):482-9 [11779051.001]
  • (PMID = 17257403.001).
  • [ISSN] 1477-7800
  • [Journal-full-title] International seminars in surgical oncology : ISSO
  • [ISO-abbreviation] Int Semin Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC1796548
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8. Kulkarni MP, Agashe SR, Singh RV, Sulhyan KR: Hepatic angiosarcoma arising in an adult mesenchymal hamartoma. Indian J Pathol Microbiol; 2010 Apr-Jun;53(2):322-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Hepatic angiosarcoma arising in an adult mesenchymal hamartoma.
  • Embryonal (undifferentiated) sarcomas arising in mesenchymal hamartoma are on record but cases of hepatic angiosarcoma (AS) arising in mesenchymal hamartoma (MH) of the liver are extremely rare.
  • [MeSH-major] Hamartoma / complications. Hamartoma / diagnosis. Hemangiosarcoma / diagnosis. Hemangiosarcoma / pathology. Liver Neoplasms / diagnosis. Liver Neoplasms / pathology
  • [MeSH-minor] Abdomen / pathology. Abdomen / ultrasonography. Histocytochemistry. Humans. Male. Microscopy. Young Adult

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  • (PMID = 20551545.001).
  • [ISSN] 0974-5130
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] India
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9. Peramiquel L, Barnadas MA, Sancho J, Curell R, Alonso MC, Fuentes MJ, Pernas S, Gómez A, Alomar A: [Angiosarcoma in an irradiated breast: a case description]. Actas Dermosifiliogr; 2005 Nov;96(9):602-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Angiosarcoma in an irradiated breast: a case description].
  • [Transliterated title] Angiosarcoma en mama irradiada: descripción de un caso.
  • Post-radiotherapy cutaneous angiosarcomas have been described in different locations, including the breast.
  • We present a case of cutaneous angiosarcoma of the breast, diagnosed 6 years after a carcinoma of the breast had been treated with radiation.
  • Considering the patient's symptoms, history and the changes observed via mammography, it was decided to completely excise the lesion followed by a simple mastectomy, with the diagnosis of angiosarcoma being confirmed.
  • Despite this fact, two years and one month later, the angiosarcoma recurred on the internal area of the mastectomy scar.
  • This complication usually appears 5-10 years after treatment with radiotherapy, so angiosarcoma should be ruled out if any angiomatous lesions later appear on skin that had been irradiated.
  • [MeSH-major] Breast Neoplasms / etiology. Breast Neoplasms / radiotherapy. Carcinoma, Ductal, Breast / radiotherapy. Hemangiosarcoma / etiology. Neoplasms, Radiation-Induced / etiology. Skin Neoplasms / etiology
  • [MeSH-minor] Adult. Female. Humans

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  • (PMID = 16476306.001).
  • [ISSN] 0001-7310
  • [Journal-full-title] Actas dermo-sifiliográficas
  • [ISO-abbreviation] Actas Dermosifiliogr
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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10. Ortiz Mendoza CM: [Recurrent breast haematoma after fine needle aspiration biopsy of angiosarcoma]. Ginecol Obstet Mex; 2007 Mar;75(3):164-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Recurrent breast haematoma after fine needle aspiration biopsy of angiosarcoma].
  • [Transliterated title] Hematoma mamario recidivante posterior a la biopsia por aspiración con aguja delgada en un angiosarcoma.
  • It is reported a rare complication after a fine needle aspiration biopsy of a breast angiosarcoma.
  • Four months later a recurrence presented, and a new excision was carried out with a resulting moderately differentiated angiosarcoma, then a simple mastectomy was performed for definitive treatment.
  • A recurrent haematoma after a fine needle aspiration biopsy of a breast tumor mandates to rule out an angiosarcoma.
  • [MeSH-major] Biopsy, Fine-Needle / adverse effects. Breast / injuries. Breast Neoplasms / pathology. Hemangiosarcoma / pathology. Hematoma / etiology
  • [MeSH-minor] Adult. Female. Humans. Mastectomy. Recurrence

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  • (PMID = 17547091.001).
  • [ISSN] 0300-9041
  • [Journal-full-title] Ginecología y obstetricia de México
  • [ISO-abbreviation] Ginecol Obstet Mex
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Mexico
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11. Amonkar GP, Deshpande JR: Cardiac angiosarcoma. Cardiovasc Pathol; 2006 Jan-Feb;15(1):57-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cardiac angiosarcoma.
  • Myxoma is the most common primary cardiac tumor, while angiosarcoma is the commonest primary malignant tumor.
  • A complete autopsy was performed and a diagnosis of cardiac angiosarcoma was confirmed on histology and immunohistochemistry.
  • [MeSH-major] Heart Neoplasms / pathology. Hemangiosarcoma / secondary
  • [MeSH-minor] Adult. Fatal Outcome. Heart Atria / pathology. Humans. Immunohistochemistry. Lung Neoplasms / secondary. Male

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  • (PMID = 16414459.001).
  • [ISSN] 1054-8807
  • [Journal-full-title] Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
  • [ISO-abbreviation] Cardiovasc. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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12. Glazebrook KN, Magut MJ, Reynolds C: Angiosarcoma of the breast. AJR Am J Roentgenol; 2008 Feb;190(2):533-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the breast.
  • OBJECTIVE: This article describes the imaging findings, pathologic correlation, and clinical presentation of rare primary and secondary angiosarcomas of the breast.
  • CONCLUSION: With the increasing use of breast conservation therapy for breast cancer, reports of postirradiation angiosarcoma have increased.
  • Both primary and secondary angiosarcomas may present with bruiselike skin discoloration, which may delay the diagnosis.
  • [MeSH-major] Breast Neoplasms / diagnosis. Diagnostic Imaging / methods. Hemangiosarcoma / diagnosis. Image Enhancement / methods
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Female. Humans. Middle Aged

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  • (PMID = 18212243.001).
  • [ISSN] 1546-3141
  • [Journal-full-title] AJR. American journal of roentgenology
  • [ISO-abbreviation] AJR Am J Roentgenol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 18
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13. Liu ZH, Lee ST, Jung SM, Tu PH: Primary spinal angiosarcoma. J Clin Neurosci; 2010 Mar;17(3):387-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary spinal angiosarcoma.
  • Primary angiosarcoma of the spine is rare.
  • To our knowledge, primary angiosarcoma in the posterior element of the spine has not been reported previously.
  • [MeSH-major] Hemangiosarcoma. Spinal Neoplasms
  • [MeSH-minor] Adult. Embolization, Therapeutic / methods. Humans. Magnetic Resonance Imaging / methods. Male. Neurosurgical Procedures / methods. Tomography, X-Ray Computed / methods

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  • [Copyright] Copyright 2009 Elsevier Ltd. All rights reserved.
  • (PMID = 20074966.001).
  • [ISSN] 1532-2653
  • [Journal-full-title] Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
  • [ISO-abbreviation] J Clin Neurosci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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14. Nayar S, Nayar PG, Cherian K: Angiosarcoma presenting as syncope. Asian Cardiovasc Thorac Ann; 2008 Apr;16(2):154-6
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  • [Title] Angiosarcoma presenting as syncope.
  • Histopathology revealed a high grade angiosarcoma.
  • This case report highlights the clinical presentation, rapid and aggressive course of cardiac angiosarcomas.
  • [MeSH-major] Heart Neoplasms / complications. Hemangiosarcoma / complications. Syncope / etiology
  • [MeSH-minor] Adult. Anemia / etiology. Cardiac Surgical Procedures. Fatal Outcome. Female. Heart Atria / pathology. Humans. Neoplasm Metastasis. Pericardial Effusion / etiology. Treatment Outcome

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  • (PMID = 18381877.001).
  • [ISSN] 1816-5370
  • [Journal-full-title] Asian cardiovascular & thoracic annals
  • [ISO-abbreviation] Asian Cardiovasc Thorac Ann
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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15. Pink D, Rahm J, Schoeler D, Schoenknecht TM, Reichardt P: Activity of paclitaxel in radiation induced and other secondary angiosarcomas. J Clin Oncol; 2009 May 20;27(15_suppl):10578

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Activity of paclitaxel in radiation induced and other secondary angiosarcomas.
  • : 10578 Background: Angiosarcomas (AS) represent 1-2% of adult soft tissue sarcomas and can arise anywhere in the body.
  • Paclitaxel has shown an exceptionally high activity of 75-89% in angiosarcomas of the face and scalp and to a lesser and less consitent degree of 15-58% in other disease locations.
  • We report on a retrospectice single center experience with chemotherapy in 17 patients (pts.) with secondary angiosarcomas (SAS).
  • 12 female patients suffered from angiosarcoma of the breast/thoracic wall following operation and radiation + chemotherapy of a primary breast cancer with an interval of a median of 6 years (range 2-15 years).
  • CONCLUSIONS: Paclitaxel shows high activity in SAS, comparable to the results in face and scalp angiosarcomas and can be considered a standard treatment option.

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  • (PMID = 27963758.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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16. Lahat G, Dhuka AR, Hallevi H, Xiao L, Zou C, Smith KD, Phung TL, Pollock RE, Benjamin R, Hunt KK, Lazar AJ, Lev D: Angiosarcoma: clinical and molecular insights. Ann Surg; 2010 Jun;251(6):1098-106
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma: clinical and molecular insights.
  • OBJECTIVE: Angiosarcoma (AS) is a rare understudied soft tissue sarcoma exhibiting endothelial cell differentiation.
  • [MeSH-major] Hemangiosarcoma / mortality
  • [MeSH-minor] Adaptor Proteins, Signal Transducing / metabolism. Adolescent. Adult. Aged. Aged, 80 and over. Benzamides. Biomarkers, Tumor / analysis. Combined Modality Therapy. DNA-Binding Proteins / metabolism. Female. Humans. Immunohistochemistry. Male. Microarray Analysis. Middle Aged. Neoplasm Metastasis. Neoplasm Recurrence, Local. Phosphoproteins / metabolism. Phosphotransferases / antagonists & inhibitors. Prognosis. Proto-Oncogene Proteins c-akt / metabolism. Proto-Oncogene Proteins c-kit / metabolism. Receptor, Epidermal Growth Factor / metabolism. Survival Rate. Transcription Factors / metabolism. Vascular Endothelial Growth Factor A / metabolism. Young Adult

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  • (PMID = 20485141.001).
  • [ISSN] 1528-1140
  • [Journal-full-title] Annals of surgery
  • [ISO-abbreviation] Ann. Surg.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / R01 CA138345
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Adaptor Proteins, Signal Transducing; 0 / Benzamides; 0 / Biomarkers, Tumor; 0 / DNA-Binding Proteins; 0 / EIF4EBP1 protein, human; 0 / ELF4 protein, human; 0 / Phosphoproteins; 0 / Transcription Factors; 0 / Vascular Endothelial Growth Factor A; 82558-50-7 / isoxaben; EC 2.7.- / Phosphotransferases; EC 2.7.10.1 / Proto-Oncogene Proteins c-kit; EC 2.7.10.1 / Receptor, Epidermal Growth Factor; EC 2.7.11.1 / Proto-Oncogene Proteins c-akt
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17. Hsu JT, Chen HM, Lin CY, Yeh CN, Hwang TL, Jan YY, Chen MF: Primary angiosarcoma of the spleen. J Surg Oncol; 2005 Dec 15;92(4):312-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the spleen.
  • BACKGROUND AND OBJECTIVES: Primary splenic angiosarcoma is a very rare and aggressive neoplasm with a high metastatic rate and dismal prognosis.
  • METHODS: The records of all cases of primary splenic angiosarcoma treated at Chang Gung Memorial Hospital from April 1991 to July 2004 were retrospectively reviewed.
  • CONCLUSIONS: The clinical presentations of splenic angiosarcoma were similar to those of previous reports apart from the higher rate of splenomegaly observed in this study.
  • [MeSH-major] Hemangiosarcoma. Splenic Neoplasms
  • [MeSH-minor] Adult. Aged. Child. Disease-Free Survival. Female. Gastrointestinal Hemorrhage / etiology. Hemoperitoneum / etiology. Humans. Male. Middle Aged. Prognosis. Retrospective Studies. Splenectomy. Splenic Rupture / etiology. Splenomegaly / etiology. Thrombocytopenia / etiology

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  • [Copyright] 2005 Wiley-Liss, Inc.
  • (PMID = 16299797.001).
  • [ISSN] 0022-4790
  • [Journal-full-title] Journal of surgical oncology
  • [ISO-abbreviation] J Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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18. Lahat G, Dhuka AR, Lahat S, Smith KD, Pollock RE, Hunt KK, Ravi V, Lazar AJ, Lev D: Outcome of locally recurrent and metastatic angiosarcoma. Ann Surg Oncol; 2009 Sep;16(9):2502-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Outcome of locally recurrent and metastatic angiosarcoma.
  • BACKGROUND: Angiosarcoma (AS) is a rare soft tissue sarcoma with an enhanced propensity for local and systemic failure.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Hemangiosarcoma / secondary. Neoplasm Recurrence, Local / pathology. Neoplasms / pathology
  • [MeSH-minor] Adolescent. Adult. Aged. Aged, 80 and over. Combined Modality Therapy. Female. Humans. Lymphatic Metastasis. Male. Middle Aged. Neoplasm Staging. Prognosis. Radiotherapy Dosage. Retrospective Studies. Survival Rate. Treatment Outcome. Young Adult

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  • (PMID = 19551444.001).
  • [ISSN] 1534-4681
  • [Journal-full-title] Annals of surgical oncology
  • [ISO-abbreviation] Ann. Surg. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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19. Tatsas AD, Keedy VL, Florell SR, Simpson JF, Coffin CM, Kelley MC, Cates JM: Foamy cell angiosarcoma: a rare and deceptively bland variant of cutaneous angiosarcoma. J Cutan Pathol; 2010 Aug;37(8):901-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Foamy cell angiosarcoma: a rare and deceptively bland variant of cutaneous angiosarcoma.
  • Cutaneous angiosarcoma can sometimes mimic other benign and malignant lesions, thereby presenting a difficult differential diagnosis.
  • In the two cases of cutaneous angiosarcoma presented herein, extensive foamy cell alteration of tumor cells resembled a reactive xanthogranulomatous process.
  • Foamy cell angiosarcoma is an unusual and deceptively benign morphologic variant of cutaneous angiosarcoma.
  • [MeSH-major] Foam Cells / pathology. Granuloma / pathology. Head and Neck Neoplasms / pathology. Hemangiosarcoma / pathology. Skin Neoplasms / pathology. Xanthomatosis / pathology
  • [MeSH-minor] Aged. Diagnosis, Differential. Forehead / pathology. Humans. Male. Shoulder / pathology. Young Adult

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  • (PMID = 20175826.001).
  • [ISSN] 1600-0560
  • [Journal-full-title] Journal of cutaneous pathology
  • [ISO-abbreviation] J. Cutan. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
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20. van der Lee C, Klootwijk PJ, van Geuns RJ, Maat LP, den Bakker MA: Angiosarcoma of the right atrium presenting as collapse. Int J Cardiol; 2009 Feb 6;132(1):e17-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the right atrium presenting as collapse.
  • Angiosarcoma is the most common cardiac malignancy, which often arises as a mass in the right atrium.
  • We describe a young patient with collapse due to pericardial effusion caused by a primary cardiac angiosarcoma.
  • The case is an example of the difficulties and dilemmas which may be encountered in assessing the diagnosis of cardiac angiosarcoma.
  • [MeSH-major] Heart Neoplasms / complications. Hemangiosarcoma / complications. Pericardial Effusion / etiology. Unconsciousness / etiology
  • [MeSH-minor] Adult. Diagnosis, Differential. Dizziness. Dyspnea. Fatal Outcome. Heart Atria. Humans. Lung Neoplasms / radiography. Lung Neoplasms / secondary. Male. Pericardiocentesis

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  • (PMID = 18031846.001).
  • [ISSN] 1874-1754
  • [Journal-full-title] International journal of cardiology
  • [ISO-abbreviation] Int. J. Cardiol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Netherlands
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21. Losanoff JE, Jaber S, Esuba M, Perry M, Sauter ER: Primary angiosarcoma of the breast: do enlarged axillary nodes matter? Breast J; 2006 Jul-Aug;12(4):371-4
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  • [Title] Primary angiosarcoma of the breast: do enlarged axillary nodes matter?
  • Primary angiosarcoma of the breast is a rare and aggressive malignancy that is typically seen in premenopausal patients.
  • We present a case of breast angiosarcoma presenting with enlarged axillary lymph nodes treated with a modified mastectomy and axillary lymph node dissection.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology. Lymph Nodes / pathology
  • [MeSH-minor] Adult. Axilla. Female. Humans. Lymph Node Excision / methods. Mastectomy, Modified Radical

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  • (PMID = 16848851.001).
  • [ISSN] 1075-122X
  • [Journal-full-title] The breast journal
  • [ISO-abbreviation] Breast J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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22. Kim JB, Kim SH, Lim SY, Roh SY, Cho GY, Song HJ, Park S, Lee J, Kim SJ: Primary angiosarcoma of the pulmonary trunk mimicking pulmonary thromboembolism. Echocardiography; 2010 Feb;27(2):E23-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the pulmonary trunk mimicking pulmonary thromboembolism.
  • We present a case of primary angiosarcoma of the pulmonary trunk that was initially misdiagnosed as a subacute massive pulmonary thromboembolism in a 26-year-old woman.
  • This is an extremely rare disease that is usually indistinguishable from acute or chronic thromboembolic disease of the pulmonary arteries because the clinical and radiologic findings of pulmonary artery angiosarcoma are similar to those of pulmonary thromboembolism.
  • Although the incidence of pulmonary artery angiosarcoma is very low, our case demonstrates that this disease entity should be included in the differential diagnosis of pulmonary thromboembolism, especially in patients who do not respond to anticoagulant therapy or present with no identifiable source of thromboembolic events.
  • [MeSH-major] Hemangiosarcoma / ultrasonography. Pulmonary Artery / ultrasonography. Vascular Neoplasms / ultrasonography
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans. Pulmonary Embolism / ultrasonography

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  • (PMID = 20380673.001).
  • [ISSN] 1540-8175
  • [Journal-full-title] Echocardiography (Mount Kisco, N.Y.)
  • [ISO-abbreviation] Echocardiography
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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23. Castilla E, Pascual I, Roncalés F, Aguirre E, Del Río A: Transient response of cardiac angiosarcoma to paclitaxel. Eur J Cancer Care (Engl); 2010 Sep;19(5):699-700
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Transient response of cardiac angiosarcoma to paclitaxel.
  • We present here the case of a patient with primary cardiac angiosarcoma that highlights the misdiagnosis at clinical presentation, current diagnostic modalities and a possible new treatment using paclitaxel for cardiac angiosarcoma.
  • [MeSH-major] Antineoplastic Agents, Phytogenic / therapeutic use. Heart Neoplasms / drug therapy. Hemangiosarcoma / drug therapy. Paclitaxel / therapeutic use
  • [MeSH-minor] Adult. Fatal Outcome. Humans. Male. Treatment Outcome

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  • (PMID = 19912298.001).
  • [ISSN] 1365-2354
  • [Journal-full-title] European journal of cancer care
  • [ISO-abbreviation] Eur J Cancer Care (Engl)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antineoplastic Agents, Phytogenic; P88XT4IS4D / Paclitaxel
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24. Yanada M, Shimada J, Ito K, Terauchi K, Shimomura M: [Cardiac angiosarcoma with diagnostic difficulty]. Kyobu Geka; 2007 Dec;60(13):1148-51
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Cardiac angiosarcoma with diagnostic difficulty].
  • We report a case of cardiac angiosarcoma of the right atrium.
  • Pathohistologically, the tumor was diagnosed as a cardiac angiosarcoma.
  • [MeSH-major] Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Biopsy. CA-125 Antigen / blood. Female. Heart Atria. Humans

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  • (PMID = 18078079.001).
  • [ISSN] 0021-5252
  • [Journal-full-title] Kyobu geka. The Japanese journal of thoracic surgery
  • [ISO-abbreviation] Kyobu Geka
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / CA-125 Antigen
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25. Liu H, Zhao J, Fan Y, Fu XL, Fu L: [Clinical and pathologic characteristics of primary angiosarcoma of breast]. Zhonghua Bing Li Xue Za Zhi; 2006 Oct;35(10):598-601
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Clinical and pathologic characteristics of primary angiosarcoma of breast].
  • OBJECTIVE: To study the clinical and pathologic characteristics of primary angiosarcoma of breast.
  • METHODS: Five cases of primary angiosarcoma of breast were reviewed.
  • CONCLUSIONS: Primary angiosarcoma of breast is a rare entity.
  • [MeSH-major] Breast Neoplasms / pathology. Breast Neoplasms, Male / pathology. Hemangiosarcoma / pathology
  • [MeSH-minor] Adult. Antigens, CD31 / metabolism. Antigens, CD34 / metabolism. Breast / metabolism. Breast / pathology. Breast / surgery. Diagnosis, Differential. Female. Follow-Up Studies. Humans. Immunohistochemistry. Male. Mastectomy / methods. Middle Aged. von Willebrand Factor / metabolism

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  • (PMID = 17134567.001).
  • [ISSN] 0529-5807
  • [Journal-full-title] Zhonghua bing li xue za zhi = Chinese journal of pathology
  • [ISO-abbreviation] Zhonghua Bing Li Xue Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / Antigens, CD31; 0 / Antigens, CD34; 0 / von Willebrand Factor
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26. Zhou YM, Li B, Yin ZM, Xu F, Wang B, Xu W, Liu P, Yang JM: Results of hepatic resection for primary hepatic angiosarcoma in adults. Med Sci Monit; 2010 Feb;16(2):CR61-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Results of hepatic resection for primary hepatic angiosarcoma in adults.
  • BACKGROUND: Primary hepatic angiosarcoma is an uncommon but aggressive malignancy with poor prognosis.
  • MATERIAL/METHODS: Medical records of 6 patients who underwent surgical resection for primary hepatic angiosarcoma at our institution between 1998 and 2006 were reviewed retrospectively.
  • CONCLUSIONS: Although the overall outcome of surgical resection remains unsatisfactory, complete surgical resection may prolong survival of patients with solitary primary hepatic angiosarcoma without spontaneous rupture.
  • [MeSH-major] Hemangiosarcoma / surgery. Liver Neoplasms / surgery
  • [MeSH-minor] Adult. Aged. Antineoplastic Agents / therapeutic use. Chemotherapy, Adjuvant. Female. Humans. Immunohistochemistry. Male. Middle Aged. Postoperative Complications / etiology. Postoperative Complications / pathology. Preoperative Care. Tomography, X-Ray Computed. Treatment Outcome

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  • (PMID = 20110916.001).
  • [ISSN] 1643-3750
  • [Journal-full-title] Medical science monitor : international medical journal of experimental and clinical research
  • [ISO-abbreviation] Med. Sci. Monit.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Poland
  • [Chemical-registry-number] 0 / Antineoplastic Agents
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27. Scow JS, Reynolds CA, Degnim AC, Petersen IA, Jakub JW, Boughey JC: Primary and secondary angiosarcoma of the breast: the Mayo Clinic experience. J Surg Oncol; 2010 Apr 1;101(5):401-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary and secondary angiosarcoma of the breast: the Mayo Clinic experience.
  • BACKGROUND AND OBJECTIVES: Angiosarcoma of the breast can be divided into primary and secondary.
  • The objective was to determine clinicopathologic factors associated with breast angiosarcoma and to compare primary versus secondary angiosarcoma.
  • METHODS: Breast angiosarcoma cases at Mayo Clinic from 1960 to 2008 were identified.
  • Characteristics of primary and secondary angiosarcoma were compared.
  • RESULTS: Twenty-seven cases of primary angiosarcoma and 14 cases of secondary angiosarcoma were identified.
  • The median age of primary angiosarcoma patients was lower than that of secondary angiosarcoma--43 years versus 73 years (P < 0.0001).
  • Primary angiosarcoma more frequently presented with a mass, whereas secondary angiosarcoma presented with a rash (P < 0.0001).
  • Median time from radiation to secondary angiosarcoma diagnosis was 6.8 years.
  • Median tumor size was 7.0 cm for primary angiosarcoma and 5.0 cm for secondary angiosarcoma (P = 0.7).
  • Tumors were high grade in 33% of primary angiosarcoma and 82% of secondary angiosarcoma (P = 0.02).
  • Five-year survival for primary and secondary angiosarcoma was 46% and 69%, respectively (P = 0.8).
  • CONCLUSION: Primary angiosarcoma occurs in younger patients than secondary and more frequently presents with a mass.
  • Mastectomy is the mainstay of treatment for breast angiosarcoma.
  • Breast angiosarcoma is a rare malignancy with poor long-term prognosis.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology. Neoplasms, Second Primary / pathology
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Female. Humans. Mastectomy. Mastectomy, Segmental. Middle Aged. Retrospective Studies

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  • [Copyright] (c) 2010 Wiley-Liss, Inc.
  • (PMID = 20119983.001).
  • [ISSN] 1096-9098
  • [Journal-full-title] Journal of surgical oncology
  • [ISO-abbreviation] J Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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28. Carnero López B, Fernández Pérez I, Carrasco Alvarez JA, Lázaro Quintela ME, López Jato C, Jorge Fernández M, Gentil González M, Vázquez Tuñas L, Castellanos Díez J: Renal primary angiosarcoma. Clin Transl Oncol; 2007 Dec;9(12):806-10
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  • [Title] Renal primary angiosarcoma.
  • Angiosarcomas account for 2% of all soft tissue sarcomas and of them, primary renal angiosarcomas represent 1%.
  • [MeSH-major] Hemangiosarcoma / pathology. Kidney Neoplasms / pathology
  • [MeSH-minor] Adult. Combined Modality Therapy. Fatal Outcome. Female. Humans. Tomography, X-Ray Computed

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  • [Cites] South Med J. 1997 Nov;90(11):1159-60 [9386065.001]
  • [Cites] Pathologe. 2001 Sep;22(5):343-8 [11572116.001]
  • [Cites] J Clin Oncol. 2001 Mar 1;19(5):1238-47 [11230464.001]
  • [Cites] Arch Pathol Lab Med. 1998 Oct;122(10):929-35 [9786357.001]
  • [Cites] Am J Kidney Dis. 1986 Aug;8(2):131-3 [3740062.001]
  • [Cites] Int J Urol. 1997 Jan;4(1):90-3 [9179675.001]
  • [Cites] Pathol Int. 1997 Nov;47(11):778-83 [9413038.001]
  • [Cites] J Chemother. 2006 Apr;18(2):221-4 [16736893.001]
  • [Cites] Gac Med Mex. 2004 Jul-Aug;140(4):463-6 [15456157.001]
  • [Cites] Arch Pathol Lab Med. 2002 Apr;126(4):478-80 [11900578.001]
  • [Cites] Lancet. 2001 Sep 22;358(9286):966-70 [11583750.001]
  • [Cites] Int Braz J Urol. 2006 Jul-Aug;32(4):448-50 [16953913.001]
  • [Cites] Cancer. 1996 Jun 1;77(11):2400-6 [8635113.001]
  • [Cites] J Urol. 2004 Mar;171(3):1071-6 [14767273.001]
  • [Cites] Scand J Urol Nephrol. 1995 Mar;29(1):103-8 [7618041.001]
  • [Cites] Cancer. 2005 Jul 15;104(2):361-6 [15948172.001]
  • [Cites] Urol Oncol. 2006 Jul-Aug;24(4):307-12 [16818182.001]
  • [Cites] Cancer. 1999 Nov 15;86(10):2034-7 [10570428.001]
  • [Cites] Tumori. 2001 Nov-Dec;87(6):439-43 [11989602.001]
  • (PMID = 18158986.001).
  • [ISSN] 1699-048X
  • [Journal-full-title] Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
  • [ISO-abbreviation] Clin Transl Oncol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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29. Yau T, Leong CH, Chan WK, Chan JK, Liang RH, Epstein RJ: A case of mixed adult Wilms' tumour and angiosarcoma responsive to carboplatin, etoposide and vincristine (CEO). Cancer Chemother Pharmacol; 2008 Apr;61(4):717-20
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case of mixed adult Wilms' tumour and angiosarcoma responsive to carboplatin, etoposide and vincristine (CEO).
  • Here we report an unusual case of mixed Wilms' tumour and angiosarcoma in a 38-year-old female patient who presented with haematuria and right lower back pain.
  • Histopathology revealed differentiated adult Wilms' tumour with renal angiosarcoma, whereas the pathology of the para-aortic lymph node and bone metastasis revealed angiosarcoma only.
  • This case suggests that highly angiogenic tumours such as angiosarcoma may be effectively palliated using agents usually reserved for refractory Wilms' tumour, and supports the view that adult Wilms' tumour is more sensitive to such agents.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Hemangiosarcoma / drug therapy. Kidney Neoplasms / drug therapy. Wilms Tumor / drug therapy
  • [MeSH-minor] Adult. Antineoplastic Agents / administration & dosage. Antineoplastic Agents, Phytogenic / administration & dosage. Carboplatin / administration & dosage. Combined Modality Therapy. Etoposide / administration & dosage. Fatal Outcome. Female. Humans. Magnetic Resonance Imaging. Neoplasm Metastasis. Neoplasm Recurrence, Local. Platelet Count. Tomography, X-Ray Computed. Vincristine / administration & dosage

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  • (PMID = 17571263.001).
  • [ISSN] 0344-5704
  • [Journal-full-title] Cancer chemotherapy and pharmacology
  • [ISO-abbreviation] Cancer Chemother. Pharmacol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Antineoplastic Agents, Phytogenic; 5J49Q6B70F / Vincristine; 6PLQ3CP4P3 / Etoposide; BG3F62OND5 / Carboplatin
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30. Bernathova M, Jaschke W, Pechlahner C, Zelger B, Bodner G: Primary angiosarcoma of the breast associated Kasabach-Merritt syndrome during pregnancy. Breast; 2006 Apr;15(2):255-8
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  • [Title] Primary angiosarcoma of the breast associated Kasabach-Merritt syndrome during pregnancy.
  • Primary angiosarcoma of the breast is a rare aggressive tumour of unknown etiology.
  • An uncommon clinical presentation of an angiosarcoma is spontaneous bleeding due to disseminated intravascular coagulation (DIC) by consumption coagulopathy, known as the Kasabach-Merritt syndrome.
  • Imaging characteristics of a breast angiosarcoma are limited to a few radiological reports.
  • We report a case of a young pregnant woman with a bleeding angiosarcoma of the breast and associated Kasabach-Merritt syndrome and describe the sonographic and MRI findings.
  • [MeSH-major] Breast Neoplasms / diagnosis. Disseminated Intravascular Coagulation / diagnosis. Hemangiosarcoma / diagnosis. Pregnancy Complications, Hematologic / diagnosis. Pregnancy Complications, Neoplastic / diagnosis
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans. Magnetic Resonance Imaging. Pregnancy. Pregnancy Trimester, Second. Prenatal Diagnosis. Syndrome

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  • (PMID = 16000250.001).
  • [ISSN] 0960-9776
  • [Journal-full-title] Breast (Edinburgh, Scotland)
  • [ISO-abbreviation] Breast
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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31. Brylka D, Demos TC, Pierce K: Primary angiosarcoma of the abdominal aorta: a case report and literature review (aortic angiosarcoma). Abdom Imaging; 2009 Mar-Apr;34(2):239-42
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the abdominal aorta: a case report and literature review (aortic angiosarcoma).
  • Fewer than 140 cases of aortic sarcoma have been reported with only 34 classified as angiosarcoma.
  • Angiosarcoma was an unexpected pathologic diagnosis based on tissue removed during aortobifemoral bypass surgery.
  • [MeSH-major] Aorta, Abdominal. Hemangiosarcoma / radiography. Vascular Neoplasms / radiography
  • [MeSH-minor] Adult. Back Pain / etiology. Fatal Outcome. Female. Humans. Immunohistochemistry. Tomography, X-Ray Computed

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  • (PMID = 18253778.001).
  • [ISSN] 1432-0509
  • [Journal-full-title] Abdominal imaging
  • [ISO-abbreviation] Abdom Imaging
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 14
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32. Champeaux-Orange E, Bonneau C, Raharimanana B, Favre A, Ibrahim M, Breteau N: [Primary breast angiosarcoma: two case reports]. Cancer Radiother; 2009 Jun;13(3):209-12
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Primary breast angiosarcoma: two case reports].
  • Primary angiosarcoma is a rare type of breast cancer, the diagnosis is difficult to establish and it has the worst prognostic of all breast malignancies.
  • Two cases of primary breast angiosarcoma have been observed at the centre Henry Kaplan of Tours and at the hospital La Source of Orleans since 2001.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology
  • [MeSH-minor] Adult. Chemotherapy, Adjuvant. Fatal Outcome. Female. Humans. Mastectomy. Middle Aged. Neoplasm Metastasis. Neoplasm Recurrence, Local. Radiotherapy, Adjuvant

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  • (PMID = 19410492.001).
  • [ISSN] 1278-3218
  • [Journal-full-title] Cancer radiothérapie : journal de la Société française de radiothérapie oncologique
  • [ISO-abbreviation] Cancer Radiother
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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33. Bhattacharya P, Singh P, Bahal A, Gulati D, Tevatia MS, Mehta A, Muttagikar MP: Angiosarcoma of pericardium: a report of two cases. Indian J Pathol Microbiol; 2007 Oct;50(4):777-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of pericardium: a report of two cases.
  • Angiosarcomas are uncommon malignant neoplasms characterized by rapidly proliferating extensively infiltrating anaplastic cells derived from blood vessels and lining irregular, blood-filled spaces.
  • Here we present two cases of pericardial angiosarcoma, one of them showing widespread dissemination, which caused considerable diagnostic dilemma and the diagnosis could only be established very late in their course of disease.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Hemangiosarcoma / pathology. Pericardium / pathology
  • [MeSH-minor] Adult. Fatal Outcome. Humans. Male. Middle Aged. Neoplasm Metastasis / diagnosis. Neoplasm Metastasis / pathology

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  • (PMID = 18306551.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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34. O'Callaghan DS, Breen DP, Young V: Angiosarcoma of the right atrium masquerading as recurrent pulmonary embolism. Thorac Cardiovasc Surg; 2008 Dec;56(8):488-90
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the right atrium masquerading as recurrent pulmonary embolism.
  • Primary cardiac angiosarcoma is a rare tumor that may present with features mimicking venous thromboembolic disease, making the diagnosis particularly challenging.
  • We report a case of angiosarcoma masquerading as recurrent pulmonary embolism successfully treated by radical surgery and adjuvant cytotoxic chemotherapy.
  • [MeSH-major] Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis. Pulmonary Embolism / diagnosis
  • [MeSH-minor] Adult. Diagnosis, Differential. Heart Aneurysm. Humans. Male. Recurrence

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  • (PMID = 19012217.001).
  • [ISSN] 0171-6425
  • [Journal-full-title] The Thoracic and cardiovascular surgeon
  • [ISO-abbreviation] Thorac Cardiovasc Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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35. Mekinian A, Lambert M, Queyrel V, Launay D, Morell-Dubois S, Hachulla E, Mathurin P, Hatron PY: [Adult-onset Still's disease and hepatic angiosarcoma, a fortuitous association or a paraneoplastic syndrome: a case-report]. Rev Med Interne; 2008 Nov;29(11):936-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Adult-onset Still's disease and hepatic angiosarcoma, a fortuitous association or a paraneoplastic syndrome: a case-report].
  • Adult-onset Still's disease is a systemic disorder without specific histological feature.
  • Nevertheless, patients with paraneoplastic adult-onset Still's disease have been reported.
  • We report a patient with an adult-onset Still's disease who presented with a liver involvement at onset.
  • Two years later, a liver angiosarcoma was diagnosed.
  • This report underlines the difficulty of the diagnosis of the adult-onset Still's disease even in the presence of Yamaguchi et al.
  • 's [Medicine 81 (2002) 194-200] classification criteria and may suggest a link between the initial clinical picture and the discovery nearly two years later, of a liver angiosarcoma.

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  • (PMID = 18572281.001).
  • [ISSN] 0248-8663
  • [Journal-full-title] La Revue de medecine interne
  • [ISO-abbreviation] Rev Med Interne
  • [Language] FRE
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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36. Chen TJ, Chiou CC, Chen CH, Kuo TT, Hong HS: Metastasis of mediastinal epithelioid angiosarcoma to the finger. Am J Clin Dermatol; 2008;9(3):181-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metastasis of mediastinal epithelioid angiosarcoma to the finger.
  • Epithelioid angiosarcoma (EA) is a rare malignant, vascular tumor that is usually observed in middle-aged and elderly males.
  • [MeSH-minor] Adult. Biopsy. Diagnosis, Differential. Fatal Outcome. Female. Humans

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  • (PMID = 18429648.001).
  • [ISSN] 1175-0561
  • [Journal-full-title] American journal of clinical dermatology
  • [ISO-abbreviation] Am J Clin Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] New Zealand
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37. Shet T, Malaviya A, Nadkarni M, Kakade A, Parmar V, Badwe R, Chinoy R: Primary angiosarcoma of the breast: observations in Asian Indian women. J Surg Oncol; 2006 Oct 1;94(5):368-74
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the breast: observations in Asian Indian women.
  • BACKGROUND: Primary angiosarcomas of breast are rare tumors, with a fatal outcome.
  • MATERIAL AND METHODS: We studied histological prognostic factors and c-kit expression by immunohistochemistry (IHC) in 12 angiosarcomas accessioned at a cancer referral center in India.
  • RESULTS: All patients had primary angiosarcoma; no case of secondary angiosarcoma was accessioned during the study period.
  • Interesting cases encountered included an epithelioid angiosarcoma and an angiosarcoma arising on the background of a biphasic tumor.
  • The patient with well-differentiated angiosarcoma also died of metastasis albeit after a longer time.
  • CONCLUSION: Primary angiosarcoma was fatal in young Indian women even in lower grade tumors.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology. Proto-Oncogene Proteins c-kit / biosynthesis
  • [MeSH-minor] Adult. Asian Continental Ancestry Group / statistics & numerical data. Female. Humans. Immunohistochemistry. India / epidemiology. Mastectomy, Segmental. Middle Aged. Neoplasm Staging. Prognosis

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  • [Copyright] Copyright (c) 2006 Wiley-Liss, Inc.
  • (PMID = 16967461.001).
  • [ISSN] 0022-4790
  • [Journal-full-title] Journal of surgical oncology
  • [ISO-abbreviation] J Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] EC 2.7.10.1 / Proto-Oncogene Proteins c-kit
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38. Batzios S, Michalopoulos A, Kaklamanis L, Stathopoulos J, Christopoulou M, Koutantos J, Stathopoulos GP: Angiosarcoma of the heart: case report and review of the literature. Anticancer Res; 2006 Nov-Dec;26(6C):4837-42
Hazardous Substances Data Bank. EPIRUBICIN .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the heart: case report and review of the literature.
  • BACKGROUND: Primary angiosarcoma of the heart is an extremely rare malignant disease.
  • PATIENTS AND METHODS: A 32-year-old female with primary angiosarcoma of the heart at an advanced stage with lung and bone metastases is presented.
  • CONCLUSION: This case of angiosarcoma of the heart is presented because of the extreme rarity of this disease, and its responsiveness to chemotherapy in combination with imatinib and herceptin.
  • [MeSH-major] Heart Neoplasms / pathology. Hemangiosarcoma / pathology
  • [MeSH-minor] Adult. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Bone Neoplasms / secondary. Cisplatin / administration & dosage. Epirubicin / administration & dosage. Female. Humans. Ifosfamide / administration & dosage. Lung Neoplasms / secondary

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  • (PMID = 17214349.001).
  • [ISSN] 0250-7005
  • [Journal-full-title] Anticancer research
  • [ISO-abbreviation] Anticancer Res.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Greece
  • [Chemical-registry-number] 3Z8479ZZ5X / Epirubicin; Q20Q21Q62J / Cisplatin; UM20QQM95Y / Ifosfamide
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39. Fujita T, Taira N, Ogasawara Y, Omori M, Doihara H: Bilateral angiosarcoma of the breast detected by magnetic resonance imaging during pregnancy. Int J Clin Oncol; 2009 Dec;14(6):560-3
MedlinePlus Health Information. consumer health - Tumors and Pregnancy.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Bilateral angiosarcoma of the breast detected by magnetic resonance imaging during pregnancy.
  • Angiosarcoma of the breast is an aggressive malignancy of endothelial origin with a tendency for local regional recurrence.
  • The involvement of angiosarcomas in the bilateral breasts has rarely been documented.
  • Here we present a rare case of bilateral angiosarcoma of the breast during pregnancy.
  • Diagnosed as angiosarcoma preoperatively, excision of the bilateral tumors was performed.
  • Histological findings of the removed bilateral tumors were compatible with high-grade angiosarcoma of the breast.
  • [MeSH-major] Breast Neoplasms / diagnosis. Hemangiosarcoma / diagnosis. Magnetic Resonance Imaging. Mammary Glands, Human / pathology. Pregnancy Complications, Neoplastic / diagnosis
  • [MeSH-minor] Adult. Female. Humans. Pregnancy

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  • [Cites] Aust N Z J Surg. 1990 May;60(5):341-5 [2334356.001]
  • [Cites] Radiother Oncol. 1996 Jan;38(1):25-31 [8850423.001]
  • [Cites] Cancer. 1983 Jun 1;51(11):2105-11 [6682350.001]
  • [Cites] Breast. 2006 Apr;15(2):255-8 [16000250.001]
  • [Cites] Cancer. 1980 Jul 15;46(2):368-71 [7190060.001]
  • [Cites] Cancer. 1965 Mar;18:352-61 [14268437.001]
  • [Cites] Histopathology. 2006 Jan;48(1):106-14 [16359542.001]
  • [Cites] Br J Surg. 1959 May;46:647-9 [13797475.001]
  • [Cites] Radiology. 1992 Jun;183(3):649-54 [1584913.001]
  • (PMID = 19967497.001).
  • [ISSN] 1437-7772
  • [Journal-full-title] International journal of clinical oncology
  • [ISO-abbreviation] Int. J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  •  go-up   go-down


40. Stoian I, Piser IT, Kulcsar I, Chioncel O, Carp A, Macarie C: Rare tumors of the heart--angiosarcoma, pericardial lipoma, leiomyosarcoma. Three case reports. J Med Life; 2010 Apr-Jun;3(2):178-82
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rare tumors of the heart--angiosarcoma, pericardial lipoma, leiomyosarcoma. Three case reports.
  • Three cases of surgically/biopsy proven angiosarcoma of the right atrium, pericardial lipoma and leiomyosarcoma of inferior vena cava--demonstrated by ultrasound, computed tomography (CT) and magnetic resonance imaging (MRI)--are presented here.
  • [MeSH-major] Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis. Leiomyosarcoma / diagnosis. Lipoma / diagnosis
  • [MeSH-minor] Adult. Echocardiography. Female. Heart Atria. Humans. Magnetic Resonance Imaging. Middle Aged. Pericardium. Tomography, X-Ray Computed. Vena Cava, Inferior

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  • [Cites] Australas Radiol. 2000 Aug;44(3):321-4 [10974728.001]
  • [Cites] Surg Today. 2004;34(4):370-3 [15052457.001]
  • [Cites] Expert Rev Cardiovasc Ther. 2008 Oct;6(9):1217-22 [18939909.001]
  • [Cites] Am J Clin Oncol. 2009 Aug;32(4):436-42 [19657238.001]
  • (PMID = 20968205.001).
  • [ISSN] 1844-122X
  • [Journal-full-title] Journal of medicine and life
  • [ISO-abbreviation] J Med Life
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Romania
  • [Other-IDs] NLM/ PMC3019051
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41. Kikawa Y, Konishi Y, Nakamoto Y, Harada T, Takeo M, Ogata M, Yamamoto M, Usuki N, Toyoshima M, Katsuyama E: Angiosarcoma of the breast - specific findings of MRI. Breast Cancer; 2006;13(4):369-73
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the breast - specific findings of MRI.
  • We present a case of low-grade angiosarcoma of the breast.
  • Core needle biopsy was performed, and a possible angiosarcoma was diagnosed.
  • It is not easy to diagnose the mammary angiosarcoma.
  • [MeSH-major] Breast Neoplasms / diagnosis. Hemangiosarcoma / diagnosis. Magnetic Resonance Imaging
  • [MeSH-minor] Adult. Contrast Media. Female. Humans. Mastectomy, Simple. Organometallic Compounds

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  • (PMID = 17146165.001).
  • [ISSN] 1340-6868
  • [Journal-full-title] Breast cancer (Tokyo, Japan)
  • [ISO-abbreviation] Breast Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Contrast Media; 0 / Organometallic Compounds; 1BJ477IO2L / gadobutrol
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42. Brenn T, Fletcher CD: Radiation-associated cutaneous atypical vascular lesions and angiosarcoma: clinicopathologic analysis of 42 cases. Am J Surg Pathol; 2005 Aug;29(8):983-96
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Radiation-associated cutaneous atypical vascular lesions and angiosarcoma: clinicopathologic analysis of 42 cases.
  • Cutaneous angiosarcoma is a rare but well-recognized complication after radiation therapy.
  • A total of 42 cases diagnosed as either radiation-associated cutaneous vascular lesions or angiosarcoma were retrieved from departmental and consultation files from 1995 to 2003.
  • Angiosarcomas presented as larger lesions (median, 7.5 cm) compared with AVLs (median, 0.5 cm).
  • The time interval from radiation was significantly shorter for the development of AVL (median, 3.5 years) compared with cutaneous angiosarcoma (median, 6 years).
  • Histologic evaluation revealed 26 lesions meeting criteria for angiosarcoma, ranging from morphologically low-grade to high-grade; 16 cases were classified as AVLs.
  • All patients with systemic relapse had an initial diagnosis of angiosarcoma.
  • One patient with an AVL had a recurrence at the same site, 3 patients developed additional new lesions, and 1 patient developed multiple small papules on the chest wall, which progressed from an AVL to angiosarcoma.
  • [MeSH-major] Hemangiosarcoma / etiology. Hemangiosarcoma / pathology. Neoplasms, Radiation-Induced / pathology. Skin / blood supply. Skin / pathology. Skin Neoplasms / etiology. Skin Neoplasms / pathology
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Breast Neoplasms / radiotherapy. Female. Follow-Up Studies. Humans. Middle Aged. Neoplasm Recurrence, Local. Neoplasms / radiotherapy. Time Factors

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  • (PMID = 16006792.001).
  • [ISSN] 0147-5185
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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43. Cantú De León D, Pérez Montiel D, Chanona Vilchis J: Unusual case of subcutaneous angiosarcoma metastatic to the ovary. Pathol Oncol Res; 2007;13(4):379-81
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Unusual case of subcutaneous angiosarcoma metastatic to the ovary.
  • Metastatic sarcomas are very rare in ovary and most of them arise from genital tract.
  • We present the case of a 33-year-old woman with subcutaneous angiosarcoma who had metastatic disease to the ovary resulting in acute abdominal pain.
  • [MeSH-major] Hemangiosarcoma / pathology. Ovarian Neoplasms / secondary. Soft Tissue Neoplasms / pathology
  • [MeSH-minor] Adult. Female. Humans. Tomography, X-Ray Computed

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  • [Cites] Gynecol Oncol. 2003 May;89(2):314-7 [12713997.001]
  • [Cites] Gynecol Oncol. 1999 Jun;73(3):443-6 [10366476.001]
  • [Cites] Int J Gynecol Pathol. 1987;6(2):166-75 [3692671.001]
  • [Cites] Cancer. 1984 May 1;53(9):1978-84 [6322966.001]
  • [Cites] Int J Gynecol Pathol. 1997 Jan;16(1):76-8 [8986536.001]
  • [Cites] Obstet Gynecol. 1956 Nov;8(5):636-8 [13370044.001]
  • [Cites] Gynecol Oncol. 1995 Oct;59(1):124-8 [7557597.001]
  • [Cites] Int J Surg Pathol. 2001 Oct;9(4):317-21 [12574850.001]
  • [Cites] Int J Gynecol Pathol. 1990;9(3):231-52 [2373588.001]
  • [Cites] Gynecol Oncol. 1992 Jan;44(1):83-6 [1730431.001]
  • [Cites] Cancer. 1984 Mar 1;53(5):1164-74 [6692304.001]
  • [Cites] Surg Gynecol Obstet. 1981 Jul;153(1):42-4 [7244973.001]
  • [Cites] Arch Gynecol Obstet. 1988;243(2):111-4 [3401039.001]
  • [Cites] Gynecol Oncol. 2004 Apr;93(1):87-91 [15047218.001]
  • [Cites] Obstet Gynecol. 1975 Apr;45(4):391-6 [1121370.001]
  • (PMID = 18158577.001).
  • [ISSN] 1219-4956
  • [Journal-full-title] Pathology oncology research : POR
  • [ISO-abbreviation] Pathol. Oncol. Res.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
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44. Kurian KC, Weisshaar D, Parekh H, Berry GJ, Reitz B: Primary cardiac angiosarcoma: case report and review of the literature. Cardiovasc Pathol; 2006 Mar-Apr;15(2):110-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary cardiac angiosarcoma: case report and review of the literature.
  • The tumor was successfully resected during surgery, and the pathological examination revealed primary cardiac angiosarcoma.
  • The case highlights the misdiagnosis in initial clinical presentation, current diagnostic modalities, and treatment options for cardiac angiosarcoma.
  • [MeSH-major] Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Heart Atria. Humans. Male

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  • (PMID = 16533700.001).
  • [ISSN] 1054-8807
  • [Journal-full-title] Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
  • [ISO-abbreviation] Cardiovasc. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 10
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45. Pohar-Marinsek Z, Lamovec J: Angiosarcoma in FNA smears: diagnostic accuracy, morphology, immunocytochemistry and differential diagnoses. Cytopathology; 2010 Oct;21(5):311-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma in FNA smears: diagnostic accuracy, morphology, immunocytochemistry and differential diagnoses.
  • OBJECTIVE: The aim of our study was to analyse the diagnostic accuracy in recognizing angiosarcoma from fine needle aspiration (FNA) samples and to determine morphological features of angiosarcoma in cytology.
  • METHODS: FNA samples from 18 histologically confirmed angiosarcomas obtained between 1985 and 2009 were included in the study.
  • RESULTS: There were 13 primary angiosarcomas and five recurrent tumours; nine tumours were epithelioid.
  • Cytomorphology did not correlate well with histology in mixed and spindle cell types of angiosarcomas.
  • CONCLUSIONS: Angiosarcomas are difficult to recognize on FNA smears when they lack the typical dual, spindle and epithelioid cell population and when they occur in internal organs where carcinomas are more common.
  • [MeSH-major] Hemangiosarcoma / pathology
  • [MeSH-minor] Adult. Aged. Antigens, CD31. Biomarkers, Tumor / metabolism. Biopsy, Fine-Needle. Cytodiagnosis. Diagnosis, Differential. Diagnostic Errors. Epithelioid Cells / metabolism. Epithelioid Cells / pathology. Female. Humans. Immunohistochemistry. Male. Middle Aged. Neoplasm Recurrence, Local. Reproducibility of Results

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  • (PMID = 20105214.001).
  • [ISSN] 1365-2303
  • [Journal-full-title] Cytopathology : official journal of the British Society for Clinical Cytology
  • [ISO-abbreviation] Cytopathology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antigens, CD31; 0 / Biomarkers, Tumor
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46. Lin CF, DeFrias D, Lin X: Epithelioid angiosarcoma: a neoplasm with potential diagnostic challenges. Diagn Cytopathol; 2010 Feb;38(2):154-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Epithelioid angiosarcoma: a neoplasm with potential diagnostic challenges.
  • Epithelioid angiosarcomas are extremely rare tumors associated with poor prognosis and early metastases.
  • Further, immunohistochemical evaluation demonstrated positive CD31 and Factor VIII staining and established the final diagnosis of epithelioid angiosarcoma.
  • This case is reported to illustrate the importance of considering the diagnosis of epithelioid angiosarcoma when encountering an "epithelioid" neoplasm particularly with unusual immunoreactivity for CK7 and CD30.
  • [MeSH-minor] Adenocarcinoma / pathology. Diagnosis, Differential. Humans. Immunohistochemistry. Liver Neoplasms / secondary. Male. Young Adult

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  • (PMID = 19813270.001).
  • [ISSN] 1097-0339
  • [Journal-full-title] Diagnostic cytopathology
  • [ISO-abbreviation] Diagn. Cytopathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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47. Biswas T, Tang P, Muhs A, Ling M: Angiosarcoma of the breast: a rare clinicopathological entity. Am J Clin Oncol; 2009 Dec;32(6):582-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the breast: a rare clinicopathological entity.
  • OBJECTIVES: Angiosarcoma is a rare subtype of sarcoma that usually arises after radiation therapy for primary breast cancer.
  • Primary sarcomas of the breast are rare entities and account for less than 1% of all malignant breast neoplasms.
  • We examine our institutional experience with angiosarcomas of the breast that were diagnosed and treated between 1996 and 2007.
  • METHODS: To conduct a retrospective review, all female patients with a diagnosis of angiosarcoma of the breast were identified from our pathology database.
  • RESULTS: A total of 8 patients were identified who had a histologically confirmed diagnosis of angiosarcoma of the breast.
  • Seven (87%) patients had a history of prior radiation to the breast, whereas 1 (13%) had primary angiosarcoma.
  • CONCLUSIONS: Even though angiosarcomas are rare neoplasms, they are increasingly recognized as the result of more breast-conserving therapy.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology. Neoplasms, Radiation-Induced / pathology. Neoplasms, Second Primary / pathology
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Combined Modality Therapy. Female. Humans. Middle Aged. Neoplasm Staging. Prognosis. Retrospective Studies. Survival Rate. Treatment Outcome

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  • (PMID = 19581792.001).
  • [ISSN] 1537-453X
  • [Journal-full-title] American journal of clinical oncology
  • [ISO-abbreviation] Am. J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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48. Syed SP, Martin AM, Haupt HM, Arenas-Elliot CP, Brooks JJ: Angiostatin receptor annexin II in vascular tumors including angiosarcoma. Hum Pathol; 2007 Mar;38(3):508-13
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiostatin receptor annexin II in vascular tumors including angiosarcoma.
  • Thirty-eight (38) vascular tumors tested included: hemangiomas - capillary [4], cavernous [6], lobular capillary [6], intramuscular hemangioma [3], spindle cell [1], and epithelioid hemangioma [4]; epithelioid hemangioendothelioma [3]; angiosarcoma [7], 4 of which were epithelioid; and angiolipomas [4].
  • Epithelioid angiosarcomas showed predominantly membranous staining.
  • To our knowledge this is the first demonstration of an angiostatin receptor (ANX2) in vascular endothelial tumors including angiosarcoma.
  • ANX2 reactivity may be the basis of treatment for a variety of benign tumors, especially in pediatric patients, and may offer a new and potentially less toxic therapy for angiosarcoma.
  • [MeSH-major] Annexin A2 / metabolism. Hemangioma / metabolism. Hemangiosarcoma / metabolism. Neoplasms, Vascular Tissue / metabolism
  • [MeSH-minor] Adolescent. Adult. Aged. Aged, 80 and over. Female. Humans. Male. Middle Aged

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  • (PMID = 17239928.001).
  • [ISSN] 0046-8177
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Annexin A2
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49. Arai E, Shimizu M, Ogawa F, Hirose T, Ohbayashi H, Taguchi S, Tsuchida T: Extravascular papillary endothelial hyperplasia of the palm masquerading as an angiosarcoma. J Dermatol; 2008 Apr;35(4):238-41
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Extravascular papillary endothelial hyperplasia of the palm masquerading as an angiosarcoma.
  • Cutaneous extravascular papillary endothelial hyperplasia (PEH) is a rare lesion presenting as a cutaneous mass and histologically mimicking angiosarcoma.
  • [MeSH-major] Hemangioendothelioma / diagnosis. Hemangiosarcoma / diagnosis. Skin Neoplasms / diagnosis
  • [MeSH-minor] Adult. Diagnosis, Differential. Hand. Humans. Male

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  • (PMID = 18419683.001).
  • [ISSN] 0385-2407
  • [Journal-full-title] The Journal of dermatology
  • [ISO-abbreviation] J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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50. Palta M, Morris CG, Grobmyer SR, Copeland EM 3rd, Mendenhall NP: Angiosarcoma after breast-conserving therapy: long-term outcomes with hyperfractionated radiotherapy. Cancer; 2010 Apr 15;116(8):1872-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma after breast-conserving therapy: long-term outcomes with hyperfractionated radiotherapy.
  • BACKGROUND: With breast-conserving therapy (BCT) as the standard of care for patients with noninvasive and early stage invasive breast cancer, a small incidence of post-BCT angiosarcoma has emerged.
  • The current study was conducted to report the long-term outcomes of a novel approach using hyperfractionated and accelerated radiotherapy (HART) for angiosarcoma developing after BCT.
  • METHODS: The authors retrospectively reviewed the outcomes of 14 patients treated with HART with or without surgery at the University of Florida between November 1997 and March 2006 for angiosarcoma that developed after BCT.
  • Five patients had further manifestations of angiosarcoma after HART at a median of 1 month (range, 1-28 months): 3 with progressive pulmonary and/or mediastinal disease that was likely present before HART and 2 with local or regional disease extension.
  • CONCLUSIONS: To the best of the authors' knowledge, HART with or without subsequent surgery, as documented in the current series, is the first approach to provide a high rate of local control, disease-free survival, and overall survival after the development of post-BCT angiosarcoma.
  • [MeSH-major] Breast Neoplasms / radiotherapy. Breast Neoplasms / surgery. Dose Fractionation. Hemangiosarcoma / cerebrospinal fluid. Hemangiosarcoma / radiotherapy
  • [MeSH-minor] Adult. Aged. Disease-Free Survival. Female. Humans. Mastectomy, Segmental. Middle Aged. Neoplasms, Second Primary / radiotherapy. Retrospective Studies. Treatment Outcome

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  • [Copyright] (c) 2010 American Cancer Society.
  • (PMID = 20162708.001).
  • [ISSN] 0008-543X
  • [Journal-full-title] Cancer
  • [ISO-abbreviation] Cancer
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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51. Fonder MA, Douglas DK: Angiosarcoma complicating systemic sclerosis: a case report. Cutis; 2008 Jun;81(6):468-72
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  • [Title] Angiosarcoma complicating systemic sclerosis: a case report.
  • Cutaneous angiosarcoma is a rare malignant vascular tumor with a poor prognosis, most commonly affecting elderly white men.
  • Cutaneous angiosarcoma has been associated with a number of conditions and factors, including chronic lymphedema, prior radiation therapy, exposure to chemicals, and vascular malformations.
  • We report the case of a 40-year-old black man with systemic sclerosis (SSc) who developed a cutaneous angiosarcoma in an area of sclerodermatous scalp.
  • We propose that vascular endothelial growth factor (VEGF) overexpression in sclerodermatous skin may predispose a patient to the development of vascular tumors, such as angiosarcoma.
  • Because early diagnosis and treatment positively impact survival outcome in patients with angiosarcoma, it is essential that physicians recognize the association of angiosarcoma and SSc and maintain a low threshold for performing a biopsy when suspicious lesions are present on sclerodermatous skin.
  • [MeSH-major] Head and Neck Neoplasms / etiology. Hemangiosarcoma / etiology. Scalp. Scleroderma, Systemic / complications. Skin Neoplasms / etiology
  • [MeSH-minor] Adult. Humans. Male


52. Valeviciene N, Mataciunas M, Tamosiunas A, Petrulioniene Z, Briediene R: Primary heart angiosarcoma detected by magnetic resonance imaging. Acta Radiol; 2006 Sep;47(7):675-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary heart angiosarcoma detected by magnetic resonance imaging.
  • We present a case of primary heart angiosarcoma in a 38-year-old male.
  • Biopsy performed through thoracoscopy confirmed the diagnosis of a primary heart angiosarcoma.
  • [MeSH-major] Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis. Magnetic Resonance Imaging / methods
  • [MeSH-minor] Adult. Biopsy. Contrast Media. Diagnosis, Differential. Echocardiography. Gadolinium DTPA. Humans. Male. Tomography, X-Ray Computed

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  • (PMID = 16950704.001).
  • [ISSN] 0284-1851
  • [Journal-full-title] Acta radiologica (Stockholm, Sweden : 1987)
  • [ISO-abbreviation] Acta Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Sweden
  • [Chemical-registry-number] 0 / Contrast Media; 84F6U3J2R6 / gadodiamide; K2I13DR72L / Gadolinium DTPA
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53. Ishigami N, Horiba K: Primary cardiac angiosarcoma resection combined with right coronary artery bypass grafting. Jpn J Thorac Cardiovasc Surg; 2005 Nov;53(11):624-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary cardiac angiosarcoma resection combined with right coronary artery bypass grafting.
  • Final diagnosis was of angiosarcoma by pathological examination.
  • [MeSH-major] Coronary Artery Bypass / methods. Heart Neoplasms / surgery. Hemangiosarcoma / surgery
  • [MeSH-minor] Adult. Coronary Angiography. Echocardiography. Female. Humans. Tomography, X-Ray Computed

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  • (PMID = 16363724.001).
  • [ISSN] 1344-4964
  • [Journal-full-title] The Japanese journal of thoracic and cardiovascular surgery : official publication of the Japanese Association for Thoracic Surgery = Nihon Kyōbu Geka Gakkai zasshi
  • [ISO-abbreviation] Jpn. J. Thorac. Cardiovasc. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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54. Pigott C, Welker M, Khosla P, Higgins RS: Improved outcome with multimodality therapy in primary cardiac angiosarcoma. Nat Clin Pract Oncol; 2008 Feb;5(2):112-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Improved outcome with multimodality therapy in primary cardiac angiosarcoma.
  • DIAGNOSIS: Primary cardiac angiosarcoma of the right atrium with systemic metastases to the pericardium, superior vena cava, and lungs.
  • [MeSH-major] Antibiotics, Antineoplastic / therapeutic use. Doxorubicin / therapeutic use. Heart Neoplasms / drug therapy. Heart Neoplasms / surgery. Hemangiosarcoma / drug therapy. Hemangiosarcoma / surgery
  • [MeSH-minor] Adult. Animals. Cattle. Chemotherapy, Adjuvant. Humans. Lung Neoplasms / drug therapy. Lung Neoplasms / secondary. Male. Neoplasm Metastasis. Reconstructive Surgical Procedures

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  • (PMID = 18235443.001).
  • [ISSN] 1743-4262
  • [Journal-full-title] Nature clinical practice. Oncology
  • [ISO-abbreviation] Nat Clin Pract Oncol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antibiotics, Antineoplastic; 80168379AG / Doxorubicin
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55. Chen YB, Guo LC, Yang L, Feng W, Zhang XQ, Ling CH, Ji C, Huang JA: Angiosarcoma of the lung: 2 cases report and literature reviewed. Lung Cancer; 2010 Dec;70(3):352-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the lung: 2 cases report and literature reviewed.
  • Angiosarcoma is a kind of malignant tumors derived from vascular endothelial cell.
  • Pulmonary angiosarcomas are usually secondary tumors, and primary cases are less than 20 so far.
  • Here we presented two cases of angiosarcoma involved the lung, and we only confirmed case 2 as a primary pulmonary angiosarcoma.
  • The clinical characteristics, diagnosis, treatment options and prognosis of pulmonary angiosarcoma were reviewed in this article too.
  • [MeSH-major] Brain Neoplasms / diagnosis. Hemangiosarcoma / diagnosis. Liver Neoplasms / diagnosis. Lung Neoplasms / diagnosis
  • [MeSH-minor] Adult. Antigens, CD31 / metabolism. Antigens, CD34 / metabolism. Biopsy. Cough. Drug Therapy. Dyspnea. Fatal Outcome. Female. Hemoptysis. Humans. Immunohistochemistry. Male. Middle Aged. Prognosis. Radiography, Thoracic

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  • [Copyright] Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.
  • (PMID = 20952087.001).
  • [ISSN] 1872-8332
  • [Journal-full-title] Lung cancer (Amsterdam, Netherlands)
  • [ISO-abbreviation] Lung Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Ireland
  • [Chemical-registry-number] 0 / Antigens, CD31; 0 / Antigens, CD34
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56. Antosz Z, Zaniewski M, Kostecki J, Poreba R: Angiosarcoma arising within a Malignant Endovascular Papillary Angioendothelioma (Dabska tumor). Neuro Endocrinol Lett; 2010;31(4):454-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma arising within a Malignant Endovascular Papillary Angioendothelioma (Dabska tumor).
  • We report an angiosarcoma arising within a malignant endovascular papillary angioendothelioma (Dabska tumor) in soft tissue of the upper thigh/buttock of a 42-year-old woman.
  • Although neoplastic progression within a vascular tumor of an existing low-grade lesion into DT has been described so far, we seem to be the first to report transformation of DT into an angiosarcoma.
  • [MeSH-major] Hemangioendothelioma / pathology. Hemangiosarcoma / pathology. Neoplasms, Multiple Primary / pathology. Soft Tissue Neoplasms / pathology
  • [MeSH-minor] Adult. Buttocks / pathology. Fatal Outcome. Female. Humans

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  • (PMID = 20802459.001).
  • [ISSN] 0172-780X
  • [Journal-full-title] Neuro endocrinology letters
  • [ISO-abbreviation] Neuro Endocrinol. Lett.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Sweden
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57. Hanasono MM, Osborne MP, Dielubanza EJ, Peters SB, Gayle LB: Radiation-induced angiosarcoma after mastectomy and TRAM flap breast reconstruction. Ann Plast Surg; 2005 Feb;54(2):211-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Radiation-induced angiosarcoma after mastectomy and TRAM flap breast reconstruction.
  • Radiation-induced angiosarcoma of the breast is being reported with increasing frequency as a result of the increased use of radiation therapy in conjunction with breast conservation surgery.
  • The authors present a case of angiosarcoma occurring in a patient 6 years after undergoing mastectomy for invasive duct carcinoma with immediate transverse rectus abdominis musculocutaneous flap reconstruction followed by postoperative radiation therapy.
  • The diagnosis of angiosarcoma was made by skin biopsy performed by the patient's reconstructive surgeon on routine follow-up examination.
  • This is the first reported case of postradiation angiosarcoma occurring in a postmastectomy breast reconstructed with autogenous tissue and it is unusual in that the cancer invaded the musculocutaneous flap.
  • Diagnosis and management recommendations for radiation-induced angiosarcoma are discussed.
  • [MeSH-major] Breast Neoplasms / surgery. Carcinoma, Ductal, Breast / surgery. Hemangiosarcoma / etiology. Mastectomy, Modified Radical. Neoplasms, Radiation-Induced / surgery
  • [MeSH-minor] Adult. Biopsy, Fine-Needle. Female. Humans. Immunoenzyme Techniques. Ki-67 Antigen / metabolism. Mammaplasty. Surgical Flaps

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  • (PMID = 15655476.001).
  • [ISSN] 0148-7043
  • [Journal-full-title] Annals of plastic surgery
  • [ISO-abbreviation] Ann Plast Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Ki-67 Antigen
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58. Thompson WM, Levy AD, Aguilera NS, Gorospe L, Abbott RM: Angiosarcoma of the spleen: imaging characteristics in 12 patients. Radiology; 2005 Apr;235(1):106-15

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the spleen: imaging characteristics in 12 patients.
  • PURPOSE: To retrospectively review clinical, pathologic, and imaging features of angiosarcoma of the spleen in 12 patients.
  • Records of 12 cases of proved angiosarcoma of the spleen were accessed from the files of the Armed Forces Institute of Pathology.
  • Angiosarcoma of the spleen could be suggested in the majority of cases (83%) by using the imaging features of splenic mass with evidence of metastatic disease.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Splenic Neoplasms / diagnosis
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Female. Humans. Magnetic Resonance Imaging. Male. Middle Aged. Retrospective Studies. Tomography, X-Ray Computed

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  • [Copyright] (c) RSNA, 2005
  • (PMID = 15749977.001).
  • [ISSN] 0033-8419
  • [Journal-full-title] Radiology
  • [ISO-abbreviation] Radiology
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, U.S. Gov't, Non-P.H.S.
  • [Publication-country] United States
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59. Lee HM, Song SY, Park JO, Kim BH: Primary immature teratoma of the prostate with angiosarcoma component: its unusual response to chemotherapy. Int J Urol; 2006 Mar;13(3):305-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary immature teratoma of the prostate with angiosarcoma component: its unusual response to chemotherapy.
  • Here, we present a case of immature teratoma of prostatic origin, which included an angiosarcoma component.
  • Angiosarcoma, although quite rare, should be included in the differential diagnosis as a component of prostatic teratoma, especially in cases in which the tumor proves unresponsive to well-known chemotherapeutic protocols.
  • This is, to our knowledge, the first reported case of primary prostatic immature teratoma containing an angiosarcoma component.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Hemangiosarcoma / drug therapy. Neoplasms, Multiple Primary. Prostatic Neoplasms / drug therapy. Teratoma / drug therapy
  • [MeSH-minor] Adult. Antineoplastic Agents / administration & dosage. Biopsy, Needle. Bleomycin / administration & dosage. Bleomycin / therapeutic use. Cisplatin / administration & dosage. Cisplatin / therapeutic use. Diagnosis, Differential. Etoposide / administration & dosage. Etoposide / therapeutic use. Humans. Male. Tomography, X-Ray Computed

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  • (PMID = 16643634.001).
  • [ISSN] 0919-8172
  • [Journal-full-title] International journal of urology : official journal of the Japanese Urological Association
  • [ISO-abbreviation] Int. J. Urol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 11056-06-7 / Bleomycin; 6PLQ3CP4P3 / Etoposide; Q20Q21Q62J / Cisplatin; BEP protocol
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60. Bhalla R, Nassar A: Cardiac angiosarcoma: report of a case diagnosed by echocardiographic-guided fine-needle aspiration. Diagn Cytopathol; 2007 Mar;35(3):164-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cardiac angiosarcoma: report of a case diagnosed by echocardiographic-guided fine-needle aspiration.
  • The authors present a case of cardiac angiosarcoma diagnosed by fine-needle aspiration (FNA) in a 33-year-old male.
  • A diagnosis of cardiac angiosarcoma was made, following which, the patient underwent treatment with chemotherapy.
  • [MeSH-major] Echocardiography. Heart Neoplasms / pathology. Heart Neoplasms / ultrasonography. Hemangiosarcoma / pathology. Hemangiosarcoma / ultrasonography
  • [MeSH-minor] Adult. Biopsy, Fine-Needle. Humans. Magnetic Resonance Imaging. Male

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  • (PMID = 17415920.001).
  • [ISSN] 8755-1039
  • [Journal-full-title] Diagnostic cytopathology
  • [ISO-abbreviation] Diagn. Cytopathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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61. Mignogna C, Simonetti S, Galloro G, Magno L, De Cecio R, Insabato L: Duodenal epithelioid angiosarcoma: immunohistochemical and clinical findings. A case report. Tumori; 2007 Nov-Dec;93(6):619-21
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Duodenal epithelioid angiosarcoma: immunohistochemical and clinical findings. A case report.
  • Angiosarcomas are uncommon malignant tumors of vascular endothelium that represent less than 1% of all sarcomas.
  • The epithelioid variant of angiosarcomas is exceptionally rare, and the gastrointestinal tract is rarely involved.
  • Angiosarcomas mainly involve skin and soft tissue and rarely occur in breast, liver, bone, and spleen.
  • A duodenal reddish polypoid lesion was found, which on microscopic examination turned out to be an epithelioid angiosarcoma.
  • Epithelioid angiosarcoma is an aggressive variant of angiosarcoma and must be considered in the differential diagnosis of gastrointestinal tumors.
  • [MeSH-major] Duodenal Neoplasms / pathology. Hemangioendothelioma, Epithelioid / pathology. Hemangiosarcoma / pathology
  • [MeSH-minor] Adult. Fatal Outcome. Humans. Immunohistochemistry. Male. Melena / etiology

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  • (PMID = 18338501.001).
  • [ISSN] 0300-8916
  • [Journal-full-title] Tumori
  • [ISO-abbreviation] Tumori
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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62. Penel N, Bui BN, Bay JO, Cupissol D, Ray-Coquard I, Piperno-Neumann S, Kerbrat P, Fournier C, Taieb S, Jimenez M, Isambert N, Peyrade F, Chevreau C, Bompas E, Brain EG, Blay JY: Phase II trial of weekly paclitaxel for unresectable angiosarcoma: the ANGIOTAX Study. J Clin Oncol; 2008 Nov 10;26(32):5269-74
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Phase II trial of weekly paclitaxel for unresectable angiosarcoma: the ANGIOTAX Study.
  • PURPOSE: The objective of this phase II trial was to assess the efficacy and toxicity of weekly paclitaxel for patients with metastatic or unresectable angiosarcoma.
  • Three patients with locally advanced breast angiosarcoma presented partial response, which enabled a secondary curative-intent surgery with complete histologic response in two cases.
  • [MeSH-major] Antineoplastic Agents, Phytogenic / administration & dosage. Breast Neoplasms / drug therapy. Head and Neck Neoplasms / drug therapy. Hemangiosarcoma / drug therapy. Paclitaxel / administration & dosage. Scalp. Skin Neoplasms / drug therapy. Soft Tissue Neoplasms / drug therapy
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Disease-Free Survival. Drug Administration Schedule. Female. France / epidemiology. Humans. Infusions, Intravenous. Kaplan-Meier Estimate. Male. Middle Aged. Neoplasm Metastasis. Time Factors. Treatment Outcome

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  • (PMID = 18809609.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Clinical Trial, Phase II; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents, Phytogenic; P88XT4IS4D / Paclitaxel
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63. Lazova R, McNiff JM, Glusac EJ, Godic A: Promontory sign--present in patch and plaque stage of angiosarcoma! Am J Dermatopathol; 2009 Apr;31(2):132-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Promontory sign--present in patch and plaque stage of angiosarcoma!
  • Kaposi sarcoma is characterized by a proliferation of irregular jagged vascular channels, which partly surround preexisting blood vessels in some areas.
  • Cutaneous angiosarcoma (AS) is a malignant vascular neoplasm comprised of a meshwork of anastomosing irregular dilated vessels between collagen bundles and around skin appendages, lined by atypical endothelial cells.
  • The presence of promontory sign has not been emphasized in lesions other than Kaposi sarcoma, but seems to be a feature that is not uncommon in patch/plaque stage AS.
  • [MeSH-major] Dermis / pathology. Endothelial Cells / pathology. Hemangiosarcoma / pathology. Sarcoma, Kaposi / pathology. Skin Neoplasms / pathology
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Biopsy. Cell Division. Databases, Factual. Female. Humans. Male. Middle Aged

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  • (PMID = 19318797.001).
  • [ISSN] 1533-0311
  • [Journal-full-title] The American Journal of dermatopathology
  • [ISO-abbreviation] Am J Dermatopathol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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64. Erpolat OP, Icli F, Dogan OV, Gokaslan G, Akmansu M, Erekul S, Yucel E: Primary cardiac angiosarcoma: a case report. Tumori; 2008 Nov-Dec;94(6):892-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary cardiac angiosarcoma: a case report.
  • Cardiac angiosarcomas are malignant tumors that almost always have a poor prognosis.
  • We describe a 29-year-old man with primary cardiac angiosarcoma with multiple site metastases.
  • We discuss the diagnosis and treatment of cardiac angiosarcoma in the light of a case report.
  • [MeSH-major] Heart Neoplasms / pathology. Hemangiosarcoma / pathology
  • [MeSH-minor] Adult. Diagnosis, Differential. Humans. Male. Prognosis. Tomography, X-Ray Computed

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  • (PMID = 19267115.001).
  • [ISSN] 0300-8916
  • [Journal-full-title] Tumori
  • [ISO-abbreviation] Tumori
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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65. Arora R, Sharma A, Gupta R, Vijayaraghavan M: Cutaneous angiosarcoma in a patient with xeroderma pigmentosum. Indian J Pathol Microbiol; 2008 Oct-Dec;51(4):504-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cutaneous angiosarcoma in a patient with xeroderma pigmentosum.
  • Cutaneous angiosarcomas are aggressive neoplasms that are rarely associated with XP.
  • In this communication, we report the case of a 40-year-old male patient with XP who developed an angiosarcoma of the face and discuss the implications of this association in view of recent developments in this field.
  • [MeSH-major] Hemangiosarcoma / complications. Skin Neoplasms / complications. Xeroderma Pigmentosum / complications
  • [MeSH-minor] Adult. Humans. Male

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  • (PMID = 19008576.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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66. Abraham JA, Hornicek FJ, Kaufman AM, Harmon DC, Springfield DS, Raskin KA, Mankin HJ, Kirsch DG, Rosenberg AE, Nielsen GP, Desphpande V, Suit HD, DeLaney TF, Yoon SS: Treatment and outcome of 82 patients with angiosarcoma. Ann Surg Oncol; 2007 Jun;14(6):1953-67
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Treatment and outcome of 82 patients with angiosarcoma.
  • BACKGROUND: Angiosarcomas are an uncommon type of malignancy that are generally thought to behave usually in a locally aggressive fashion; they often metastasize to distant sites.
  • METHODS: Patients with a diagnosis of angiosarcoma treated at our institution between 1980 and 2006 were analyzed for patient demographics, tumor characteristics, multimodality treatment, and outcomes.
  • CONCLUSIONS: Primary angiosarcomas treated with aggressive surgical resection and the addition of radiation for close margins or worrisome pathologic features can result in long-term survival in most patients.
  • [MeSH-major] Hemangiosarcoma / surgery
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Bone Neoplasms / pathology. Bone Neoplasms / surgery. Breast Neoplasms / pathology. Breast Neoplasms / surgery. Chemotherapy, Adjuvant. Disease-Free Survival. Female. Follow-Up Studies. Humans. Male. Middle Aged. Neoadjuvant Therapy. Neoplasm Staging. Neoplasms, Radiation-Induced / pathology. Neoplasms, Radiation-Induced / surgery. Palliative Care. Radiotherapy, Adjuvant. Retrospective Studies. Skin Neoplasms / pathology. Skin Neoplasms / surgery. Soft Tissue Neoplasms / pathology. Soft Tissue Neoplasms / surgery. Survival Rate. Treatment Outcome

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  • (PMID = 17356953.001).
  • [ISSN] 1068-9265
  • [Journal-full-title] Annals of surgical oncology
  • [ISO-abbreviation] Ann. Surg. Oncol.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / 5K12CA87723-03
  • [Publication-type] Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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67. Schmid H, Zietz C: Human herpesvirus 8 and angiosarcoma: analysis of 40 cases and review of the literature. Pathology; 2005 Aug;37(4):284-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Human herpesvirus 8 and angiosarcoma: analysis of 40 cases and review of the literature.
  • AIMS: To prove a possible involvement of the endotheliotropic human herpesvirus 8 (HHV-8) in the pathogenesis of angiosarcoma in samples from patients in a low HHV-8 seroprevalence area.
  • METHODS: A comprehensive series of angiosarcomas (n = 40) as well as positive and negative control tissues from patients with Kaposi's sarcoma, human immunodeficiency virus (HIV)-associated multicentric Castleman's disease or juvenile haemangioma, respectively, was analysed with two sensitive methods: immunohistochemical staining for the HHV-8 latency-associated nuclear antigen 1 (LANA-1); and polymerase chain reaction (PCR) for HHV-8 VP23 DNA sequences.
  • RESULTS: None of the angiosarcoma cases and none of the negative control samples (juvenile haemangiomas) revealed positive immunohistochemical staining with the LANA-1 antibody.
  • In contrast, HHV-8 LANA-1 was clearly detected in all analysed cases of Kaposi's sarcoma and multicentric Castleman's disease.
  • CONCLUSION: In conclusion, the great majority of angiosarcomas investigated to date, including the series of 40 angiosarcomas analysed here, does not contain HHV-8 DNA sequences or protein.
  • This argues against a relevant role of the endotheliotropic HHV-8 in the pathogenesis of angiosarcoma and, for vascular diseases, speaks in favour of a relatively restricted pathogenic role of HHV-8 to Kaposi's sarcoma and multicentric Castleman's disease.
  • [MeSH-major] Hemangiosarcoma / virology. Herpesviridae Infections / epidemiology. Herpesvirus 8, Human / isolation & purification. Tumor Virus Infections / epidemiology
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Animals. Female. Giant Lymph Node Hyperplasia / virology. Humans. Immunohistochemistry. Male. Middle Aged. Oncogenic Viruses / isolation & purification. Polymerase Chain Reaction. Sarcoma, Kaposi / virology

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  • (PMID = 16194826.001).
  • [ISSN] 0031-3025
  • [Journal-full-title] Pathology
  • [ISO-abbreviation] Pathology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
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68. West JG, Weitzel JN, Tao ML, Carpenter M, West JE, Fanning C: BRCA mutations and the risk of angiosarcoma after breast cancer treatment. Clin Breast Cancer; 2008 Dec;8(6):533-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] BRCA mutations and the risk of angiosarcoma after breast cancer treatment.
  • Post-breast cancer treatment-related angiosarcomas were first observed in lymphedematous extremities after mastectomy and are now being reported with increasing frequency after lumpectomy and radiation.
  • A case history is presented of a BRCA2 carrier who had a postmastectomy chest wall angiosarcoma but had neither therapeutic radiation nor clinically evident lymphedema.
  • The absence of established risk factors led to speculation that the BRCA2 germline mutation could be a causative factor in the development of this patient's angiosarcoma.
  • [MeSH-major] BRCA2 Protein / genetics. Breast Neoplasms / surgery. Carcinoma, Ductal, Breast / surgery. Germ-Line Mutation. Hemangiosarcoma / genetics. Neoplasms, Second Primary / genetics. Skin Neoplasms / genetics
  • [MeSH-minor] Adult. Female. Genetic Predisposition to Disease. Humans. Mastectomy. Neoplasm Recurrence, Local

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  • (PMID = 19073510.001).
  • [ISSN] 1526-8209
  • [Journal-full-title] Clinical breast cancer
  • [ISO-abbreviation] Clin. Breast Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / BRCA2 Protein
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69. Pai MR, Upadhyaya K, Naik R, Malhotra S: Bilateral angiosarcoma breast diagnosed by fine needle aspiration cytology. Indian J Pathol Microbiol; 2008 Jul-Sep;51(3):421-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Bilateral angiosarcoma breast diagnosed by fine needle aspiration cytology.
  • Concurrent or synchronous angiosarcoma (AS) of breast is a rarity.
  • [MeSH-major] Breast Neoplasms / diagnosis. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Biopsy, Fine-Needle. Female. Humans. Immunohistochemistry

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  • (PMID = 18723979.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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70. Davidson B, Abeler VM: Primary ovarian angiosarcoma presenting as malignant cells in ascites: case report and review of the literature. Diagn Cytopathol; 2005 May;32(5):307-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary ovarian angiosarcoma presenting as malignant cells in ascites: case report and review of the literature.
  • Primary angiosarcoma of the ovary is a rare tumor, with less than 25 cases reported in the literature.
  • This is the first reported case of an ovarian angiosarcoma that metastasized to the peritoneal cavity, with a resulting malignant effusion.
  • Despite the rarity of metastasis from gynecological sarcomas in effusions, this possibility needs to be included in the differential diagnosis of malignant effusions that are negative for epithelial and germ cell markers.
  • [MeSH-major] Ascites / pathology. Cytodiagnosis / methods. Hemangiosarcoma / pathology. Ovarian Neoplasms / pathology
  • [MeSH-minor] Adult. Ascitic Fluid / pathology. Biomarkers, Tumor / analysis. Chemotherapy, Adjuvant. Diagnosis, Differential. Fatal Outcome. Female. Humans. Immunohistochemistry. Ovariectomy

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  • [Copyright] Copyright 2005 Wiley-Liss, Inc.
  • (PMID = 15830366.001).
  • [ISSN] 8755-1039
  • [Journal-full-title] Diagnostic cytopathology
  • [ISO-abbreviation] Diagn. Cytopathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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71. Park YS, Kim JH, Kim KW, Lee IS, Yoon HK, Ko GY, Sung KB: Primary hepatic angiosarcoma: imaging findings and palliative treatment with transcatheter arterial chemoembolization or embolization. Clin Radiol; 2009 Aug;64(8):779-85
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary hepatic angiosarcoma: imaging findings and palliative treatment with transcatheter arterial chemoembolization or embolization.
  • AIM: To describe the image findings and results of transcatheter arterial chemoembolization (TACE) or transcatheter arterial embolization (TAE) for treating primary hepatic angiosarcoma.
  • MATERIALS AND METHODS: A retrospective review of the electronic medical database from 2002 to 2007, revealed six patients with primary hepatic angiosarcoma confirmed by percutaneous liver biopsy.
  • CONCLUSIONS: Primary hepatic angiosarcoma appears as a solitary or multiple, hypervascular lesions with heterogeneously early and progressive enhancement on CT and angiography.
  • Although TAE may be the primary procedure for achieving emergent bleeding control caused by the rupture of hepatic angiosarcomas, TACE may be effective for treating patients with a dominant hepatic angiosarcoma with or without intrahepatic metastases.
  • [MeSH-major] Hemangiosarcoma / radiography. Liver Neoplasms / radiography
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Angiography / methods. Antineoplastic Agents / administration & dosage. Chemoembolization, Therapeutic / methods. Cisplatin / administration & dosage. Embolization, Therapeutic / methods. Fatal Outcome. Female. Humans. Male. Middle Aged. Palliative Care / methods. Radiography, Interventional. Retrospective Studies. Tomography, X-Ray Computed / methods. Treatment Outcome

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  • (PMID = 19589416.001).
  • [ISSN] 1365-229X
  • [Journal-full-title] Clinical radiology
  • [ISO-abbreviation] Clin Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antineoplastic Agents; Q20Q21Q62J / Cisplatin
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72. Olsun A, Duzyol C, Gur AK, Kaplan M, Tosun R: Right atrial angiosarcoma: a case report. Heart Surg Forum; 2007;10(3):E219-21

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Right atrial angiosarcoma: a case report.
  • The pathological diagnosis based on the samples obtained during the operation was angiosarcoma.
  • We believe that advancements in radiotherapy and chemotherapy regimes combined with surgery (radical, if possible) for the treatment of cardiac angiosarcomas may provide better survival and quality-of-life results.
  • [MeSH-major] Heart Neoplasms / diagnosis. Heart Neoplasms / surgery. Hemangiosarcoma / diagnosis. Hemangiosarcoma / surgery
  • [MeSH-minor] Adult. Female. Heart Atria. Humans

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  • (PMID = 17599895.001).
  • [ISSN] 1522-6662
  • [Journal-full-title] The heart surgery forum
  • [ISO-abbreviation] Heart Surg Forum
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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73. DeMartelaere SL, Roberts D, Burgess MA, Morrison WH, Pisters PW, Sturgis EM, Ho V, Esmaeli B: Neoadjuvant chemotherapy-specific and overall treatment outcomes in patients with cutaneous angiosarcoma of the face with periorbital involvement. Head Neck; 2008 May;30(5):639-46
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Neoadjuvant chemotherapy-specific and overall treatment outcomes in patients with cutaneous angiosarcoma of the face with periorbital involvement.
  • BACKGROUND: Recent isolated case reports have suggested a potential role for neoadjuvant chemotherapy in patients with angiosarcoma.
  • The goal of this report was to investigate the overall treatment outcomes and the neoadjuvant chemotherapy-specific outcomes in patients with cutaneous angiosarcoma of the face with periorbital involvement.
  • METHODS: Our tumor database was searched for patients with angiosarcoma and periorbital involvement seen at our institution between 1981 and 2005.
  • CONCLUSION: On the basis of this series, the authors conclude that neoadjuvant chemotherapy for periorbital angiosarcoma is a potentially attractive option and in some patients may obviate the need for major surgery, thereby preserving the eye and/or ocular adnexal structures.
  • [MeSH-major] Eyelid Neoplasms / therapy. Facial Neoplasms / therapy. Hemangiosarcoma / therapy. Neoadjuvant Therapy. Skin Neoplasms / therapy
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Chemotherapy, Adjuvant. Disease-Free Survival. Female. Humans. Male. Middle Aged. Neoplasm Recurrence, Local. Radiotherapy, Adjuvant. Retrospective Studies. Survival Analysis

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  • (PMID = 18213722.001).
  • [ISSN] 1043-3074
  • [Journal-full-title] Head & neck
  • [ISO-abbreviation] Head Neck
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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74. Luk A, Nwachukwu H, Lim KD, Cusimano RJ, Butany J: Cardiac angiosarcoma: a case report and review of the literature. Cardiovasc Pathol; 2010 May-Jun;19(3):e69-74

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cardiac angiosarcoma: a case report and review of the literature.
  • We present the case of a 36-year-old woman with widespread metastatic cardiac angiosarcoma to the lungs and the liver.
  • [MeSH-major] Heart Neoplasms / pathology. Hemangiosarcoma / secondary
  • [MeSH-minor] Adult. Antineoplastic Agents / therapeutic use. Cardiovascular Surgical Procedures. Combined Modality Therapy. Female. Humans. Liver Neoplasms / secondary. Liver Neoplasms / therapy. Lung Neoplasms / secondary. Lung Neoplasms / therapy. Neoadjuvant Therapy

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  • [Copyright] Copyright 2010 Elsevier Inc. All rights reserved.
  • (PMID = 19150248.001).
  • [ISSN] 1879-1336
  • [Journal-full-title] Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
  • [ISO-abbreviation] Cardiovasc. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents
  • [Number-of-references] 34
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75. Takeuchi T, Iwasaki S, Miyazaki J, Nozaki Y, Takahashi M, Ono M, Saibara T, Furihata M: Matrix metalloproteinase-1 expression in splenic angiosarcoma metastasizing to the serous membrane. Int J Clin Exp Pathol; 2010;3(6):634-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Matrix metalloproteinase-1 expression in splenic angiosarcoma metastasizing to the serous membrane.
  • Angiosarcoma involving the serous membrane may mimic mesothelioma; therefore, the term "pseudomesotheliomatous angiosarcoma" has been suggested for this entity.
  • However, the pathogenesis of pseudomesotheliomatous angiosarcoma remains unclear.
  • Here, we report an autopsy case of splenic angiosarcoma, which systemically metastasized to the serous membrane of both the peritoneum and pleura, closely resembling a mesothelioma.
  • MMP-1 expression was not observed in the other cases of angiosarcoma, examined.
  • [MeSH-major] Hemangiosarcoma / enzymology. Matrix Metalloproteinase 1 / biosynthesis. Peritoneal Neoplasms / secondary. Pleural Neoplasms / secondary. Splenic Neoplasms / enzymology
  • [MeSH-minor] Adult. Autopsy. Biomarkers, Tumor / analysis. Biomarkers, Tumor / metabolism. Fatal Outcome. Humans. Immunohistochemistry. Male. Serous Membrane / pathology. Splenectomy

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  • [Cites] J Neurochem. 2000 Apr;74(4):1489-97 [10737605.001]
  • [Cites] Proc Natl Acad Sci U S A. 2006 Sep 19;103(38):14128-33 [16966607.001]
  • [Cites] Int J Cancer. 2001 Mar 1;91(5):638-43 [11267973.001]
  • [Cites] Science. 2004 Oct 1;306(5693):108-11 [15459390.001]
  • [Cites] Am J Clin Pathol. 1976 Feb;65(2):159-67 [175652.001]
  • [Cites] Zentralbl Allg Pathol. 1979;123(4):344-50 [506520.001]
  • [Cites] Cancer. 1981 Oct 15;48(8):1907-21 [7197190.001]
  • [Cites] Arch Pathol Lab Med. 1983 Jun;107(6):304-7 [6687794.001]
  • [Cites] Arch Pathol Lab Med. 1987 May;111(5):459-63 [3105516.001]
  • [Cites] Acta Pathol Jpn. 1988 Oct;38(10):1345-51 [3218512.001]
  • [Cites] Virchows Arch A Pathol Anat Histopathol. 1991;419(5):439-45 [1750189.001]
  • [Cites] Am J Surg Pathol. 1993 Oct;17(10):959-70 [8372948.001]
  • [Cites] Am J Surg Pathol. 1996 Dec;20(12):1431-9 [8944035.001]
  • [Cites] Histopathology. 1997 May;30(5):419-24 [9181362.001]
  • [Cites] Br J Cancer. 2000 Nov;83(9):1147-53 [11027427.001]
  • (PMID = 20661412.001).
  • [ISSN] 1936-2625
  • [Journal-full-title] International journal of clinical and experimental pathology
  • [ISO-abbreviation] Int J Clin Exp Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; EC 3.4.24.7 / Matrix Metalloproteinase 1
  • [Other-IDs] NLM/ PMC2907126
  • [Keywords] NOTNLM ; Angiosarcoma / MMP-1 / collagenase-1 / pseudomesothelioma
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76. Kuroda N, Hamaguchi N, Inoue K, Ohara M, Mizuno K, Hayashi Y, Lee GH: Application of immunocytochemistry to the diagnosis of primary epithelioid angiosarcoma of the lung. Med Mol Morphol; 2009 Dec;42(4):250-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Application of immunocytochemistry to the diagnosis of primary epithelioid angiosarcoma of the lung.
  • Pulmonary epithelioid angiosarcoma is rare, and there are no descriptions of the immunocytochemistry of such a case.
  • Finally, we suggest that the immunocytochemical study of imprint cytological materials may supply available information in diagnosing angiosarcoma with epithelioid features lacking characteristic structures.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Lung Neoplasms / diagnosis. Vascular Neoplasms / diagnosis
  • [MeSH-minor] Adult. Antigens, CD31 / metabolism. Antigens, CD34 / metabolism. Epithelioid Cells / pathology. Humans. Immunohistochemistry. Male. von Willebrand Factor / metabolism

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  • [Cites] Ann Diagn Pathol. 2005 Feb;9(1):33-7 [15692948.001]
  • [Cites] Med Mol Morphol. 2008 Jun;41(2):109-12 [18592165.001]
  • [Cites] Mod Pathol. 2001 Dec;14(12):1216-25 [11743043.001]
  • [Cites] Diagn Cytopathol. 2007 Mar;35(3):171-3 [17415922.001]
  • [Cites] Ann Diagn Pathol. 2005 Oct;9(5):302-4 [16198962.001]
  • [Cites] Diagn Cytopathol. 2005 Dec;33(6):429-33 [16299742.001]
  • [Cites] Mod Pathol. 1999 Dec;12(12):1124-31 [10619264.001]
  • [Cites] Mod Pathol. 2005 May;18(5):728-32 [15578068.001]
  • [Cites] Diagn Cytopathol. 2004 May;30(5):350-2 [15108235.001]
  • [Cites] Med Mol Morphol. 2008 Jun;41(2):117-20 [18592167.001]
  • [Cites] Diagn Cytopathol. 2003 Sep;29(3):140-5 [12951681.001]
  • [Cites] Mod Pathol. 2004 May;17(5):547-52 [15001993.001]
  • [Cites] Cancer. 2000 Aug 25;90(4):245-51 [10966566.001]
  • [Cites] Am J Surg Pathol. 2001 Aug;25(8):1061-6 [11474291.001]
  • [Cites] Ann Diagn Pathol. 2005 Aug;9(4):209-14 [16084454.001]
  • [Cites] Arch Pathol Lab Med. 2005 Jan;129(1):e7-10 [15628928.001]
  • [Cites] Diagn Cytopathol. 2000 Aug;23(2):143-5 [10888763.001]
  • [Cites] Am J Surg Pathol. 2004 Mar;28(3):298-307 [15104292.001]
  • [Cites] Diagn Cytopathol. 2002 Jun;26(6):349-55 [12112823.001]
  • [Cites] Arch Pathol Lab Med. 2005 Aug;129(8):1054-6 [16048401.001]
  • (PMID = 20033373.001).
  • [ISSN] 1860-1499
  • [Journal-full-title] Medical molecular morphology
  • [ISO-abbreviation] Med Mol Morphol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Antigens, CD31; 0 / Antigens, CD34; 0 / von Willebrand Factor
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77. Nascimento AF, Raut CP, Fletcher CD: Primary angiosarcoma of the breast: clinicopathologic analysis of 49 cases, suggesting that grade is not prognostic. Am J Surg Pathol; 2008 Dec;32(12):1896-904
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the breast: clinicopathologic analysis of 49 cases, suggesting that grade is not prognostic.
  • Mammary angiosarcoma is a rare neoplasm, accounting for about 0.05% of all primary malignancies of the breast.
  • It is currently believed that histologic grading of mammary angiosarcomas plays an important role in prognostication.
  • Forty-nine cases of primary angiosarcoma of the breast were retrieved from our files.
  • In conclusion, mammary angiosarcoma is a rare disease that affects relatively younger patients.
  • This tumor seems to have an overall similar clinical course as other types of angiosarcoma arising in skin or soft tissue; it carries a moderate risk of local recurrence, and a high risk of metastasis and death.
  • In this large series, there is no correlation between histologic grade and patient outcome, more in line with angiosarcomas at other sites.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology
  • [MeSH-minor] Adolescent. Adult. Age Distribution. Aged. Disease-Free Survival. Female. Humans. Middle Aged. Prognosis

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  • (PMID = 18813119.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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78. Wang ZS, Zhan N, Xiong CL, Li H: Primary epithelioid angiosarcoma of the male breast: report of a case. Surg Today; 2007;37(9):782-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary epithelioid angiosarcoma of the male breast: report of a case.
  • We report a case of primary epithelioid angiosarcoma of the male breast.
  • Histopathological examination and immunohistochemical analysis confirmed a diagnosis of primary epithelioid angiosarcoma of the male breast, without axillary lymph node metastasis.
  • [MeSH-major] Breast Neoplasms, Male / pathology. Hemangiosarcoma / pathology. Neoplasms, Glandular and Epithelial / pathology
  • [MeSH-minor] Adult. Humans. Immunohistochemistry. Male. Sex Factors

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  • [Cites] Arch Anat Cytol Pathol. 1997;45(1):54-6 [9339005.001]
  • [Cites] Virchows Arch A Pathol Anat Histopathol. 1993;423(4):309-14 [8236827.001]
  • [Cites] Histopathology. 1999 Aug;35(2):114-20 [10460655.001]
  • [Cites] Histopathology. 1994 Mar;24(3):269-71 [7726886.001]
  • [Cites] Gan No Rinsho. 1984 Feb;30(2):167-9 [6708304.001]
  • [Cites] Cancer. 1985 Oct 15;56(8):2099-106 [4040802.001]
  • [Cites] Int J Radiat Oncol Biol Phys. 2000 Jan 15;46(2):383-90 [10661345.001]
  • [Cites] Virchows Arch. 1999 Nov;435(5):473-8 [10592050.001]
  • [Cites] Arch Surg. 1995 Feb;130(2):221-3 [7848095.001]
  • [Cites] Clin Oncol (R Coll Radiol). 2006 Jun;18(5):426-7 [16817336.001]
  • [Cites] J Surg Oncol. 1988 Oct;39(2):90-5 [3172796.001]
  • [Cites] Zhonghua Wai Ke Za Zhi. 1997 May;35(5):294-5 [10374567.001]
  • [Cites] Am J Surg. 2003 Oct;186(4):359-61 [14553850.001]
  • [Cites] Hum Pathol. 1995 Nov;26(11):1275-7 [7590704.001]
  • [Cites] Ann Pathol. 2005 Jun;25(3):235-9 [16230950.001]
  • [Cites] Am J Surg Pathol. 1994 Jan;18(1):62-73 [8279629.001]
  • [Cites] Int J Radiat Oncol Biol Phys. 1993 Oct 20;27(3):671-5 [8226163.001]
  • [Cites] Hum Pathol. 1986 Sep;17(9):906-13 [3019868.001]
  • [Cites] Am J Surg Pathol. 1998 Sep;22(9):1154-9 [9737250.001]
  • [Cites] Ophthalmology. 1983 Dec;90(12 ):1414-21 [6687155.001]
  • [Cites] J Cutan Pathol. 1995 Apr;22(2):164-7 [7560351.001]
  • [Cites] J Clin Pathol. 1998 Dec;51(12):928-30 [10070336.001]
  • [Cites] Am J Clin Pathol. 1994 Dec;102(6):757-63 [7801888.001]
  • [Cites] Breast Cancer Res Treat. 1989 Jan;13(1):39-48 [2468372.001]
  • [Cites] Am J Surg Pathol. 1991 Oct;15(10):915-24 [1718176.001]
  • [Cites] Surg Clin North Am. 1996 Apr;76(2):383-92 [8610270.001]
  • [Cites] Cancer. 1980 Jul 15;46(2):368-71 [7190060.001]
  • [Cites] Semin Diagn Pathol. 1986 Nov;3(4):259-87 [3303234.001]
  • [Cites] Am J Clin Pathol. 1994 Sep;102(3):388-9 [8085563.001]
  • [Cites] Hum Pathol. 1997 Mar;28(3):383-5 [9042806.001]
  • [Cites] Am J Surg Pathol. 1999 Nov;23(11):1418-22 [10555012.001]
  • [Cites] Am J Clin Pathol. 1994 Sep;102(3):322-30 [8085556.001]
  • [Cites] Am J Surg Pathol. 1997 May;21(5):599-604 [9158686.001]
  • [Cites] Am J Surg Pathol. 1996 Dec;20(12):1431-9 [8944035.001]
  • [Cites] Radiology. 1992 Jun;183(3):649-54 [1584913.001]
  • [Cites] Int Surg. 1988 Jul-Sep;73(3):193-5 [3068175.001]
  • [Cites] Histopathology. 2003 Jul;43(1):1-16 [12823707.001]
  • [Cites] Histopathology. 1999 Oct;35(4):319-27 [10564386.001]
  • [Cites] Neurol Med Chir (Tokyo). 1995 Jun;35(6):364-8 [7566378.001]
  • (PMID = 17713733.001).
  • [ISSN] 0941-1291
  • [Journal-full-title] Surgery today
  • [ISO-abbreviation] Surg. Today
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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79. Kinderyte R, Alisauskaite L, Juodzbaliene EB, Juozaityte E: [Angiosarcoma of the breast: a case report and literature review]. Medicina (Kaunas); 2006;42(7):580-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Angiosarcoma of the breast: a case report and literature review].
  • Sarcoma of the breast is a rare tumor (makes up 0.5 to 1% of all malignant breast tumors).
  • In literature, only isolated cases of primary angiosarcoma of the breast were described.
  • Secondary angiosarcomas are more frequently diagnosed in women and mostly in patients who underwent breast-conserving surgery and were treated by radiotherapy.
  • In this article a very rare case of angiosarcoma of the breast is presented.
  • After review of histopathology slides the likely diagnosis of angiosarcoma of the breast was made.
  • The mean survival of patients with angiosarcoma of the breast, described in literature, ranges from 13 to 22 months, and the treatment in this case most likely could not have an effect on survival of the patient.
  • [MeSH-major] Breast Neoplasms. Hemangiosarcoma
  • [MeSH-minor] Adult. Breast / pathology. Diagnosis, Differential. Female. Humans. Lung Neoplasms / radiography. Lung Neoplasms / secondary. Lymphatic Metastasis / diagnosis. Mastectomy, Simple. Prognosis. Radiography, Thoracic. Time Factors

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  • (PMID = 16861841.001).
  • [ISSN] 1648-9144
  • [Journal-full-title] Medicina (Kaunas, Lithuania)
  • [ISO-abbreviation] Medicina (Kaunas)
  • [Language] lit
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Lithuania
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80. Luini A, Gatti G, Diaz J, Botteri E, Oliveira E, Cecilio Sahium de Almeida R, Veronesi P, Intra M, Pagani G, Naninato P, Viale G: Angiosarcoma of the breast: the experience of the European Institute of Oncology and a review of the literature. Breast Cancer Res Treat; 2007 Sep;105(1):81-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the breast: the experience of the European Institute of Oncology and a review of the literature.
  • Angiosarcoma of the breast (AB) is a rare entity: its overall incidence is estimated at between 0.002% and 0.005% per year.
  • We report the experience of the European Institute of Oncology with this unusual disease from January 1996 to January 2006: sixteen patients with angiosarcoma, 9 (56%) of whom had primary AB and 7 (44%), secondary AB, are discussed.
  • [MeSH-major] Breast Neoplasms / diagnosis. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Aged. Disease-Free Survival. Europe. Female. Humans. Middle Aged. Retrospective Studies. Risk Factors. Sarcoma / diagnosis. Sarcoma / pathology. Sarcoma / radiotherapy. Soft Tissue Neoplasms / diagnosis. Soft Tissue Neoplasms / pathology. Soft Tissue Neoplasms / radiotherapy. Time Factors

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  • (PMID = 17115110.001).
  • [ISSN] 0167-6806
  • [Journal-full-title] Breast cancer research and treatment
  • [ISO-abbreviation] Breast Cancer Res. Treat.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
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81. Govender PS: Atypical presentation of angiosarcoma of the scalp in the setting of human immunodeficiency virus (HIV). World J Surg Oncol; 2009;7:99
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  • [Title] Atypical presentation of angiosarcoma of the scalp in the setting of human immunodeficiency virus (HIV).
  • BACKGROUND: Angiosarcoma of the head and neck is an uncommon, aggressive malignant entity most commonly found in elderly Caucasian males.
  • The atypical gender, age and race of the patient reflect the unusual clinical presentation of this case of angiosarcoma, attributable to the patient's HIV status.
  • [MeSH-major] HIV Infections / complications. HIV-1 / pathogenicity. Head and Neck Neoplasms / etiology. Hemangiosarcoma / etiology. Scalp / pathology
  • [MeSH-minor] Adult. Anthracyclines / administration & dosage. Antineoplastic Combined Chemotherapy Protocols. CD4 Lymphocyte Count. Combined Modality Therapy. Female. Humans. Ifosfamide / administration & dosage. Radiotherapy Dosage. Young Adult


82. Vavilis D, Papadopoulos N, Agorastos T, Efstratiou I, Kommoss F, Bontis IN: Primary ovarian angiosarcoma--review of the literature and report of a case with coexisting chylothorax. Eur J Gynaecol Oncol; 2007;28(4):287-9
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  • [Title] Primary ovarian angiosarcoma--review of the literature and report of a case with coexisting chylothorax.
  • BACKGROUND: Primary ovarian angiosarcoma is a very rare gynaecologic malignancy with poor prognosis and uncertain, up-to-date, treatment options.
  • CASE: We report a case of primary pure ovarian angiosarcoma with coexisting chylothorax which is, to the best of our knowledge, the first reported case.
  • RESULT: In spite of all therapeutic efforts, surgical and medical, prognosis of ovarian angiosarcoma remains very poor in most cases.
  • CONCLUSION: Primary ovarian angiosarcoma is a rare and aggressive malignancy.
  • [MeSH-major] Chylothorax / complications. Hemangiosarcoma / complications. Ovarian Neoplasms / complications
  • [MeSH-minor] Adult. Fatal Outcome. Female. Humans

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  • (PMID = 17713094.001).
  • [ISSN] 0392-2936
  • [Journal-full-title] European journal of gynaecological oncology
  • [ISO-abbreviation] Eur. J. Gynaecol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Italy
  • [Number-of-references] 23
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83. Puppala S, Hoey ET, Mankad K, Wood AM: Primary cardiac angiosarcoma arising from the interatrial septum: magnetic resonance imaging appearances. Br J Radiol; 2010 Nov;83(995):e230-4
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  • [Title] Primary cardiac angiosarcoma arising from the interatrial septum: magnetic resonance imaging appearances.
  • We present a case of primary cardiac angiosarcoma arising from the interatrial septum that had imaging features overlapping with those of right atrial myxoma.
  • To the best of our knowledge, this is the first reported case of angiosarcoma arising from the interatrial septum that has undergone evaluation with CMR.
  • [MeSH-major] Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis. Magnetic Resonance Imaging / methods
  • [MeSH-minor] Adult. Atrial Septum. Diagnosis, Differential. Female. Humans. Myxoma / diagnosis. Myxoma / pathology

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  • [Cites] Chest. 2000 Aug;118(2):547-9 [10936155.001]
  • [Cites] Radiographics. 2000 Jul-Aug;20(4):1073-103; quiz 1110-1, 1112 [10903697.001]
  • [Cites] Radiographics. 2002 May-Jun;22(3):673-89 [12006696.001]
  • [Cites] Am J Cardiol. 2003 Oct 1;92(7):890-5 [14516903.001]
  • [Cites] Radiographics. 2003 Oct;23 Spec No:S141-5 [14557508.001]
  • [Cites] Cancer. 1986 Feb 15;57(4):852-9 [3510706.001]
  • [Cites] Mayo Clin Proc. 1992 Oct;67(10):957-65 [1434856.001]
  • [Cites] J Am Soc Echocardiogr. 1996 Mar-Apr;9(2):209-12 [8849621.001]
  • [Cites] Cathet Cardiovasc Diagn. 1998 Apr;43(4):451-3 [9554777.001]
  • [Cites] Cardiologia. 1998 Oct;43(10):1101-3 [9922576.001]
  • [Cites] Eur Radiol. 2005 Jul;15(7):1446-55 [15627179.001]
  • [Cites] Radiographics. 2005 Sep-Oct;25(5):1255-76 [16160110.001]
  • [Cites] Cardiol Rev. 2006 Mar-Apr;14(2):101-3 [16493248.001]
  • [Cites] Radiographics. 2006 May-Jun;26(3):795-810 [16702455.001]
  • [Cites] Clin Oncol (R Coll Radiol). 2007 Dec;19(10):748-56 [17693068.001]
  • [Cites] Heart. 2008 Jan;94(1):117-23 [18083956.001]
  • [Cites] Nat Clin Pract Oncol. 2008 Feb;5(2):112-5 [18235443.001]
  • [Cites] Magn Reson Imaging Clin N Am. 2008 May;16(2):137-64, vii [18474324.001]
  • [Cites] Circulation. 2008 Sep 30;118(14 Suppl):S7-15 [18824772.001]
  • [Cites] AJR Am J Roentgenol. 2009 Aug;193(2):377-87 [19620434.001]
  • [Cites] Ann Thorac Surg. 1999 Oct;68(4):1236-41 [10543485.001]
  • [Cites] Radiographics. 2000 Sep-Oct;20(5):1303-19 [10992020.001]
  • (PMID = 20965894.001).
  • [ISSN] 1748-880X
  • [Journal-full-title] The British journal of radiology
  • [ISO-abbreviation] Br J Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC3473733
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84. Wang XY, Jakowski J, Tawfik OW, Thomas PA, Fan F: Angiosarcoma of the breast: a clinicopathologic analysis of cases from the last 10 years. Ann Diagn Pathol; 2009 Jun;13(3):147-50
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma of the breast: a clinicopathologic analysis of cases from the last 10 years.
  • Breast angiosarcoma may occur de novo, or as a complication of radiation therapy, or chronic lymphedema secondary to axillary lymph node dissection for mammary carcinoma.
  • In our effort to characterize the clinicopathologic features of breast angiosarcoma, we reviewed all breast angiosarcoma cases in the University of Kansas Medical Center and Ohio State University Medical Center archives from 1997 to 2007.
  • Only 11 angiosarcomas were identified among more than 5000 malignant breast neoplasms (0.1%-0.2% incidence) for the last 10 years.
  • Eight cases (6 high grade, 1 intermediate grade, 1 low grade) were identified as postradiation angiosarcoma (postradiation time interval, 4-12 years), and 3 cases were identified as primary angiosarcomas (1 high grade, 2 low grade).
  • Follow-up (median, 36 months) revealed that 3 cases of postradiation angiosarcoma recurred as skin and/or chest wall lesions and 1 case of primary angiosarcoma developed liver metastases (all high-grade).
  • In conclusion, breast angiosarcoma remains a rare disease.
  • Rosen's method for grading breast angiosarcoma is easy to implement and correlates well with clinical outcome.
  • There are no distinct clinical or histologic differences between primary and postradiation breast angiosarcomas.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Chemotherapy, Adjuvant. Combined Modality Therapy. Female. Humans. Mastectomy. Middle Aged. Neoplasm Recurrence, Local / epidemiology. Neoplasms, Radiation-Induced / pathology. Neoplasms, Radiation-Induced / therapy

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  • (PMID = 19433291.001).
  • [ISSN] 1532-8198
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 12
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85. Bernardos L, García Marín A, Rey Valcárcel C, Martín Gil J, Turégano Fuentes F: [Hepatic angiosarcoma]. Rev Esp Enferm Dig; 2008 Dec;100(12):804-6
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  • [Title] [Hepatic angiosarcoma].
  • [Transliterated title] Angiosarcoma hepático.
  • [MeSH-major] Hemangiosarcoma / pathology. Liver Neoplasms / pathology
  • [MeSH-minor] Adult. Female. Humans. Male. Middle Aged

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  • (PMID = 19222346.001).
  • [ISSN] 1130-0108
  • [Journal-full-title] Revista española de enfermedades digestivas : organo oficial de la Sociedad Española de Patología Digestiva
  • [ISO-abbreviation] Rev Esp Enferm Dig
  • [Language] spa
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Spain
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86. Azimi NA, Selter JG, Abott JD, Cabin HS, Hutner A, Copel J, Setaro JF: Angiosarcoma in a pregnant woman presenting with pericardial tamponade--a case report and review of the literature. Angiology; 2006 Mar-Apr;57(2):251-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma in a pregnant woman presenting with pericardial tamponade--a case report and review of the literature.
  • The authors present a rare case of pericardial tamponade complicating pregnancy with resulting diagnosis of angiosarcoma.
  • They review the literature involving pericardial disease in pregnancy and discuss important issues in management and include a discussion of angiosarcoma.
  • [MeSH-major] Cardiac Tamponade / etiology. Heart Neoplasms / complications. Hemangiosarcoma / complications. Pregnancy Complications, Neoplastic
  • [MeSH-minor] Adult. Biopsy. Cardiac Surgical Procedures / methods. Diagnosis, Differential. Echocardiography. Female. Follow-Up Studies. Heart Atria. Humans. Magnetic Resonance Imaging. Pericardial Effusion / complications. Pericardial Effusion / diagnosis. Pericardial Effusion / surgery. Pregnancy. Tomography, X-Ray Computed

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  • (PMID = 16518537.001).
  • [ISSN] 0003-3197
  • [Journal-full-title] Angiology
  • [ISO-abbreviation] Angiology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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87. Jha S, Chan KK, Poole CJ, Rollason TP: Pregnancy following recurrent angiosarcoma of the ovary--a case report and review of literature. Gynecol Oncol; 2005 Jun;97(3):935-7
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  • [Title] Pregnancy following recurrent angiosarcoma of the ovary--a case report and review of literature.
  • BACKGROUND: Ovarian angiosarcomas are rare tumors which may to be distinguished from other unusual primary ovarian tumors such as clear cell carcinoma, yolk sac tumor and leiomyosarcoma on the basis of histological appearance and immunohistochemistry.
  • Angiosarcomas of the ovary occur in all age groups but are more frequent in women of child bearing age (less than 40 years).
  • CASE: The case we present is the only reported long-term survivor of recurrent ovarian angiosarcoma.
  • CONCLUSION: Adjuvant chemotherapy of ovarian angiosarcoma with a combination of doxorubicin and ifosfamide appears effective and should be considered in women at risk of relapse who wish to conserve fertility.
  • [MeSH-major] Hemangiosarcoma / therapy. Neoplasm Recurrence, Local. Ovarian Neoplasms / therapy. Pregnancy Complications, Neoplastic
  • [MeSH-minor] Adult. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Combined Modality Therapy. Doxorubicin / administration & dosage. Female. Fertility. Humans. Ifosfamide / administration & dosage. Pregnancy

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  • (PMID = 15943995.001).
  • [ISSN] 0090-8258
  • [Journal-full-title] Gynecologic oncology
  • [ISO-abbreviation] Gynecol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 80168379AG / Doxorubicin; UM20QQM95Y / Ifosfamide
  • [Number-of-references] 15
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88. Gagner JP, Yim JH, Yang GC: Fine-needle aspiration cytology of epithelioid angiosarcoma: a diagnostic dilemma. Diagn Cytopathol; 2005 Dec;33(6):429-33

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Fine-needle aspiration cytology of epithelioid angiosarcoma: a diagnostic dilemma.
  • On the basis of cytologic features on smears, high-grade sarcoma was reported.
  • The case was sent for expert consultation, and the expert's opinion was epithelioid angiosarcoma.
  • The clinical presentation, cytology, histology, and immunohistochemistry of the current case and 15 other cases of epithelioid angiosarcoma found in the cytology literature are summarized.
  • [MeSH-major] Hemangiosarcoma / pathology. Iliac Vein / pathology. Vascular Neoplasms / pathology
  • [MeSH-minor] Adult. Biopsy, Fine-Needle. Diagnosis, Differential. Diagnostic Errors. Epithelioid Cells / pathology. Female. Humans. Immunohistochemistry. Venous Thrombosis / radiography

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  • (PMID = 16299742.001).
  • [ISSN] 8755-1039
  • [Journal-full-title] Diagnostic cytopathology
  • [ISO-abbreviation] Diagn. Cytopathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 24
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89. Sanchez-Mejia RO, Ojemann SG, Simko J, Chaudhary UB, Levy J, Lawton MT: Sacral epithelioid angiosarcoma associated with a bleeding diathesis and spinal epidural hematoma: case report. J Neurosurg Spine; 2006 Mar;4(3):246-50
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  • [Title] Sacral epithelioid angiosarcoma associated with a bleeding diathesis and spinal epidural hematoma: case report.
  • Epithelioid angiosarcoma of bone is a rare, high-grade lesion that is highly vascular and can be associated with a bleeding diathesis.
  • An association has been reported in angiosarcomas in other locations with coagulopathy from tumor-related disseminated intravascular coagulopathy and fibrinolysis.
  • The authors report the case of a rare occurrence of a primary sacral epithelioid angiosarcoma associated with a large epidural hematoma and a severe bleeding diathesis.
  • This case represents the first report of a primary epithelioid angiosarcoma in the sacrum and emphasizes that the coagulopathy seen in angiosarcoma is also a feature of this epithelioid variant.
  • [MeSH-major] Bone Neoplasms / complications. Hemangiosarcoma / complications
  • [MeSH-minor] Adult. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Blood Transfusion. Combined Modality Therapy. Doxorubicin / administration & dosage. Embolization, Therapeutic. Female. Hematoma, Epidural, Spinal. Hemorrhagic Disorders. Hemostasis. Humans. Ifosfamide / administration & dosage. Laminectomy. Magnetic Resonance Imaging. Sacrum / pathology. Sacrum / surgery. Treatment Outcome

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  • (PMID = 16572625.001).
  • [ISSN] 1547-5654
  • [Journal-full-title] Journal of neurosurgery. Spine
  • [ISO-abbreviation] J Neurosurg Spine
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 80168379AG / Doxorubicin; UM20QQM95Y / Ifosfamide
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90. Asmane I, Litique V, Heymann S, Marcellin L, Métivier AC, Duclos B, Bergerat JP, Kurtz JE: Adriamycin, cisplatin, ifosfamide and paclitaxel combination as front-line chemotherapy for locally advanced and metastatic angiosarcoma. Analysis of three case reports and review of the literature. Anticancer Res; 2008 Sep-Oct;28(5B):3041-5
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  • [Title] Adriamycin, cisplatin, ifosfamide and paclitaxel combination as front-line chemotherapy for locally advanced and metastatic angiosarcoma. Analysis of three case reports and review of the literature.
  • Angiosarcoma represents 1 to 2% of soft tissue tumors.
  • The outcome of angiosarcoma is poor for those patients in whom aggressive surgery cannot be considered.
  • We report three cases of angiosarcoma in which first-line chemotherapy with adriamycin 40 mg/m2 day 1, ifosfamide 3 g/m2 day 1-2, cisplatin 35 mg/m2 day 1-2 and paclitaxel 175 mg/m2 day 3 led to clinically meaningful responses.
  • We emphasize the need for designing trials specifically dedicated to angiosarcomas, as this rare and severe condition may be a target for new antiangiogenic drugs.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Bone Neoplasms / drug therapy. Breast Neoplasms / drug therapy. Hemangiosarcoma / drug therapy. Soft Tissue Neoplasms / drug therapy
  • [MeSH-minor] Adult. Aged. Cisplatin / administration & dosage. Doxorubicin / administration & dosage. Female. Humans. Ifosfamide / administration & dosage. Lumbar Vertebrae. Male. Middle Aged. Paclitaxel / administration & dosage. Young Adult

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  • (PMID = 19031953.001).
  • [ISSN] 0250-7005
  • [Journal-full-title] Anticancer research
  • [ISO-abbreviation] Anticancer Res.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Greece
  • [Chemical-registry-number] 80168379AG / Doxorubicin; P88XT4IS4D / Paclitaxel; Q20Q21Q62J / Cisplatin; UM20QQM95Y / Ifosfamide
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91. Fonseca V, Reis G, Lourenço C, Alves C, Vasconcelos AP, Martelo F, Bravio I, Lousinha A, Timóteo AT, Pinto E, Granadeiro J, Pinto Saraiva A: [Pulmonary metastasis in a cardiac angiosarcoma - case report and discussion]. Rev Port Pneumol; 2009 Nov-Dec;15(6):1175-84
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  • [Title] [Pulmonary metastasis in a cardiac angiosarcoma - case report and discussion].
  • Admitted to the pulmonology unit patient underwent videothoracsopy which diagnosed cardiac angiosarcoma with pulmonary metastisation.
  • [MeSH-major] Heart Neoplasms / pathology. Hemangiosarcoma / secondary. Lung Neoplasms / secondary
  • [MeSH-minor] Adult. Humans. Male

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  • (PMID = 19859633.001).
  • [ISSN] 2172-6825
  • [Journal-full-title] Revista portuguesa de pneumologia
  • [ISO-abbreviation] Rev Port Pneumol
  • [Language] por
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Portugal
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92. Cardinale L, Mirra M, Galli C, Goldblum JR, Pizzolitto S, Falconieri G: Angiosarcoma of the uterus: report of 2 new cases with deviant clinicopathologic features and review of the literature. Ann Diagn Pathol; 2008 Jun;12(3):217-21
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  • [Title] Angiosarcoma of the uterus: report of 2 new cases with deviant clinicopathologic features and review of the literature.
  • A few cases of uterine angiosarcoma have been detailed in the literature: 2 new cases are herein described featuring some unusual clinical or phenotypic differences compared with previously published cases, such as occurrence in premenopausal age or a poorly differentiated histology.
  • Occurrence in childbearing age or a deviant histologic pattern, as documented in this report, may be added to the clinicopathologic spectrum of uterine angiosarcoma.
  • [MeSH-major] Hemangiosarcoma / secondary. Uterine Neoplasms / pathology
  • [MeSH-minor] Adult. Aged, 80 and over. Antigens, CD / analysis. Biomarkers, Tumor / analysis. Diagnosis, Differential. Factor VIII / analysis. Fatal Outcome. Female. Humans. Immunohistochemistry. Leiomyosarcoma / diagnosis. Necrosis

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  • (PMID = 18486900.001).
  • [ISSN] 1532-8198
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD; 0 / Biomarkers, Tumor; 9001-27-8 / Factor VIII
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93. Farag R, Schulak JA, Abdul-Karim FW, Wasman JK: Angiosarcoma arising in an arteriovenous fistula site in a renal transplant patient: a case report and literature review. Clin Nephrol; 2005 May;63(5):408-12
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  • [Title] Angiosarcoma arising in an arteriovenous fistula site in a renal transplant patient: a case report and literature review.
  • Angiosarcoma in the setting of immunosuppressed renal transplant recipients is exceedingly rare.
  • In this report, we describe the occurrence of angiosarcoma arising at an arteriovenous fistula site of a 39-year-old renal transplant recipient that clinically mimicked a thrombosed aneurysm.
  • [MeSH-major] Arteriovenous Fistula / pathology. Hemangiosarcoma / pathology. Immunocompromised Host. Kidney Transplantation / immunology. Vascular Neoplasms / pathology
  • [MeSH-minor] Adult. Biopsy, Needle. Disease Progression. Fatal Outcome. Humans. Immunohistochemistry. Male. Risk Assessment

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  • (PMID = 15909604.001).
  • [ISSN] 0301-0430
  • [Journal-full-title] Clinical nephrology
  • [ISO-abbreviation] Clin. Nephrol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 32
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94. Scholsem M, Raket D, Flandroy P, Sciot R, Deprez M: Primary temporal bone angiosarcoma: a case report. J Neurooncol; 2005 Nov;75(2):121-5
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  • [Title] Primary temporal bone angiosarcoma: a case report.
  • We present a rare case of temporal bone angiosarcoma diagnosed in a 26-year-old female patient at 36 week of pregnancy.
  • Pathological findings were those of a poorly differentiated, highly malignant sarcoma with a large epitheloid component and immunohistochemical evidence of endothelial differentiation (CD31, Factor VIII related antigen, CD34), consistent with an angiosarcoma with epitheloid features.
  • We present a rare case of primary temporal bone angiosarcoma and report our experience with a multimode therapeutic approach combining surgery, radiotherapy and chemotherapy.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Pregnancy Complications, Neoplastic / diagnosis. Skull Neoplasms / diagnosis. Skull Neoplasms / pathology. Temporal Bone
  • [MeSH-minor] Adult. Angiography. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Bone Neoplasms / secondary. Combined Modality Therapy. Fatal Outcome. Female. Follow-Up Studies. Humans. Lung Neoplasms / secondary. Pregnancy. Pregnancy Trimester, Third. Tomography, X-Ray Computed

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  • [Cites] Ann Otol Rhinol Laryngol. 1948 Mar;57(1):235-40 [18913539.001]
  • [Cites] Cancer. 1971 Jun;27(6):1403-14 [5088217.001]
  • [Cites] J Neurosurg. 1991 Jul;75(1):73-6 [2045922.001]
  • [Cites] Laryngoscope. 1974 Mar;84(3):454-8 [4814415.001]
  • [Cites] AJNR Am J Neuroradiol. 2001 Apr;22(4):755-8 [11290494.001]
  • [Cites] Am J Otolaryngol. 1999 Jul-Aug;20(4):223-31 [10442774.001]
  • [Cites] Surg Neurol. 2004 Jun;61(6):575-9 [15165804.001]
  • [Cites] Cancer. 1982 Feb 15;49(4):727-36 [7198934.001]
  • [Cites] Neurosurgery. 1999 Feb;44(2):405-7; discussion 407-8 [9932897.001]
  • [Cites] Cancer. 1995 Feb 15;75(4):989-96 [7842420.001]
  • [Cites] Cancer Invest. 1998;16(7):442-6 [9774950.001]
  • [Cites] Ann Otol Rhinol Laryngol. 1994 Feb;103(2):156-9 [8311392.001]
  • [Cites] J Laryngol Otol. 1980 Feb;94(2):205-10 [7189541.001]
  • [Cites] South Med J. 1991 Apr;84(4):517-20 [2014445.001]
  • [Cites] Eur J Neurol. 2003 Nov;10(6):741-2 [14641524.001]
  • [Cites] Neurosurgery. 1996 Mar;38(3):583-5; discussion 585-6 [8837814.001]
  • [Cites] Histopathology. 1991 May;18(5):395-402 [1715839.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 1997 May 4;40(1):67-71 [9184980.001]
  • [Cites] Cancer. 1999 Nov 15;86(10):2034-7 [10570428.001]
  • [Cites] AJNR Am J Neuroradiol. 1996 Nov-Dec;17 (10 ):1946-8 [8933884.001]
  • [Cites] Pediatr Radiol. 1992;22(2):134-5 [1501943.001]
  • (PMID = 16132518.001).
  • [ISSN] 0167-594X
  • [Journal-full-title] Journal of neuro-oncology
  • [ISO-abbreviation] J. Neurooncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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95. Köhler HF, Neves RI, Brechtbühl ER, Mattos Granja NV, Ikeda MK, Kowalski LP: Cutaneous angiosarcoma of the head and neck: report of 23 cases from a single institution. Otolaryngol Head Neck Surg; 2008 Oct;139(4):519-24
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  • [Title] Cutaneous angiosarcoma of the head and neck: report of 23 cases from a single institution.
  • BACKGROUND: To report a single-institution experience in the treatment of cutaneous head and neck angiosarcoma.
  • [MeSH-major] Head and Neck Neoplasms / mortality. Hemangiosarcoma / mortality. Skin Neoplasms / mortality
  • [MeSH-minor] Adolescent. Adult. Aged. Child. Female. Humans. Kaplan-Meier Estimate. Male. Middle Aged. Neoplasm Recurrence, Local. Scalp. Treatment Outcome

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  • (PMID = 18922337.001).
  • [ISSN] 0194-5998
  • [Journal-full-title] Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery
  • [ISO-abbreviation] Otolaryngol Head Neck Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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96. den Bakker MA, Ansink AC, Ewing-Graham PC: "Cutaneous-type" angiosarcoma arising in a mature cystic teratoma of the ovary. J Clin Pathol; 2006 Jun;59(6):658-60
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  • [Title] "Cutaneous-type" angiosarcoma arising in a mature cystic teratoma of the ovary.
  • An angiosarcoma with "cutaneous" type typical features arising in a dermoid cyst of the ovary is reported.
  • [MeSH-major] Hemangiosarcoma / pathology. Neoplasms, Second Primary / pathology. Ovarian Neoplasms / pathology. Teratoma / pathology
  • [MeSH-minor] Adult. Female. Humans

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  • [Cites] Pathol Oncol Res. 1999;5(4):318-9 [10607929.001]
  • [Cites] Eur J Obstet Gynecol Reprod Biol. 2000 Feb;88(2):153-7 [10690674.001]
  • [Cites] Semin Diagn Pathol. 2000 Aug;17(3):225-35 [10968708.001]
  • [Cites] Int J Gynecol Pathol. 2002 Jan;21(1):16-21 [11781518.001]
  • [Cites] Am J Surg Pathol. 2003 Jan;27(1):58-64 [12502928.001]
  • [Cites] Int J Surg Pathol. 2001 Oct;9(4):317-21 [12574850.001]
  • [Cites] Virchows Arch. 2003 Oct;443(4):574-8 [12836022.001]
  • [Cites] Hum Pathol. 1985 Mar;16(3):268-72 [2982720.001]
  • [Cites] Arch Pathol Lab Med. 1986 Jan;110(1):77-8 [3753575.001]
  • [Cites] Am J Surg Pathol. 1986 Oct;10(10):711-7 [3021008.001]
  • [Cites] Mod Pathol. 1989 Jan;2(1):55-8 [2922391.001]
  • [Cites] J Clin Pathol. 1990 Sep;43(9):752-7 [2212067.001]
  • [Cites] Am J Surg Pathol. 1991 Oct;15(10):915-24 [1718176.001]
  • [Cites] Obstet Gynecol. 1971 Jun;37(6):920-41 [4378308.001]
  • [Cites] Ann Med. 1993 Jun;25(3):221-33 [8333922.001]
  • [Cites] Semin Surg Oncol. 1994 Sep-Oct;10(5):369-73 [7997731.001]
  • [Cites] Am J Surg Pathol. 1995 Jun;19(6):642-52 [7538732.001]
  • [Cites] J Cutan Pathol. 1995 Jun;22(3):215-22 [7593814.001]
  • [Cites] Aust N Z J Obstet Gynaecol. 1996 May;36(2):221-2 [8798322.001]
  • [Cites] Int J Gynecol Pathol. 1997 Oct;16(4):378-82 [9421078.001]
  • [Cites] Am J Surg Pathol. 1998 May;22(5):620-30 [9591733.001]
  • [Cites] Am J Surg Pathol. 1998 Jun;22(6):683-97 [9630175.001]
  • [Cites] Gynecol Oncol. 1999 Jun;73(3):443-6 [10366476.001]
  • [Cites] Obstet Gynecol Surv. 1957 Dec;12(6):793-830 [13493921.001]
  • [Cites] Diagn Cytopathol. 2005 May;32(5):307-9 [15830366.001]
  • (PMID = 16731607.001).
  • [ISSN] 0021-9746
  • [Journal-full-title] Journal of clinical pathology
  • [ISO-abbreviation] J. Clin. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC1860385
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97. Fury MG, Antonescu CR, Van Zee KJ, Brennan MF, Maki RG: A 14-year retrospective review of angiosarcoma: clinical characteristics, prognostic factors, and treatment outcomes with surgery and chemotherapy. Cancer J; 2005 May-Jun;11(3):241-7
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  • [Title] A 14-year retrospective review of angiosarcoma: clinical characteristics, prognostic factors, and treatment outcomes with surgery and chemotherapy.
  • PURPOSE: Angiosarcoma is a rare vascular malignancy, and there are few published data to guide chemotherapy treatment decisions.
  • We present a retrospective analysis of angiosarcoma encompassing all anatomic sites of disease presenting to a single institution over a 14-year period.
  • One hundred twenty-five patients with angiosarcoma were seen and treated between January 1, 1990 and December 31, 2003.
  • RESULTS: Angiosarcoma showed marked variation by anatomic site regarding gender ratio, median age at diagnosis, overall survival, and response to chemotherapy.
  • Overall 5-year survival was 31% for angiosarcoma.
  • For unresectable angiosarcoma, doxorubicin based regimens yielded progression-free survival of 3.7-5.4 months.
  • Paclitaxel achieved a progression-free survival of 6.8 months for scalp angiosarcoma and 2.8 months for sites below the clavicle.
  • DISCUSSION: Angiosarcoma is an aggressive malignancy characterized by biologic heterogeneity at different anatomic sites and relative sensitivity to paclitaxel and doxorubicin.
  • [MeSH-major] Antibiotics, Antineoplastic / therapeutic use. Antineoplastic Agents, Phytogenic / therapeutic use. Doxorubicin / therapeutic use. Hemangiosarcoma. Neoplasm Staging. Paclitaxel / therapeutic use
  • [MeSH-minor] Adult. Age of Onset. Aged. Aged, 80 and over. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Disease Progression. Disease-Free Survival. Female. Humans. Male. Middle Aged. Prognosis. Retrospective Studies. Sex Factors

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  • [ErratumIn] Cancer J. 2005 Jul-Aug;11(4):354
  • (PMID = 16053668.001).
  • [ISSN] 1528-9117
  • [Journal-full-title] Cancer journal (Sudbury, Mass.)
  • [ISO-abbreviation] Cancer J
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / P01 CA47179
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antibiotics, Antineoplastic; 0 / Antineoplastic Agents, Phytogenic; 80168379AG / Doxorubicin; P88XT4IS4D / Paclitaxel
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98. Nelson BL, Thompson LD: Sinonasal tract angiosarcoma: a clinicopathologic and immunophenotypic study of 10 cases with a review of the literature. Head Neck Pathol; 2007 Sep;1(1):1-12

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Sinonasal tract angiosarcoma: a clinicopathologic and immunophenotypic study of 10 cases with a review of the literature.
  • BACKGROUND: Primary sinonasal tract angiosarcoma are rare tumors that are frequently misclassified, resulting in inappropriate clinical management.
  • MATERIALS AND METHODS: Ten patients with sinonasal tract angiosarcoma were retrospectively retrieved from the Otorhinolaryngic Registry of the Armed Forces Institute of Pathology.
  • The principle differential diagnosis includes granulation tissue, lobular capillary hemangioma (pyogenic granuloma), and Kaposi's sarcoma.
  • CONCLUSIONS: Sinonasal tract angiosarcoma is a rare tumor, frequently presenting in middle-aged patients as a large mass usually involving the nasal cavity with characteristic histomorphologic and immunophenotypic features.
  • Sinonasal tract angiosarcoma will often have a poor prognosis making appropriate separation from other conditions important.
  • [MeSH-major] Hemangiosarcoma / pathology. Nasal Cavity / pathology. Paranasal Sinus Neoplasms / pathology
  • [MeSH-minor] Adolescent. Adult. Aged. Aged, 80 and over. Biomarkers, Tumor / metabolism. Diagnosis, Differential. Fatal Outcome. Female. Granulation Tissue / pathology. Granuloma, Pyogenic / diagnosis. Humans. Male. Middle Aged. Prognosis. Sarcoma, Kaposi / diagnosis. Young Adult

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  • [Cites] Arch Pathol Lab Med. 1990 Aug;114(8):825-8 [1695836.001]
  • [Cites] Histopathology. 1990 Sep;17(3):237-42 [2242851.001]
  • [Cites] J Laryngol Otol. 1990 Oct;104(10):831-4 [2246590.001]
  • [Cites] Genes Chromosomes Cancer. 1990 Mar;1(4):315-6 [2278963.001]
  • [Cites] Ear Nose Throat J. 1990 Dec;69(12):813-8 [2079004.001]
  • [Cites] Am J Clin Pathol. 1991 Jul;96(1):25-31 [1712541.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 1991 Oct;117(10):1182-4 [1910709.001]
  • [Cites] Mod Pathol. 1991 Jul;4(4):449-55 [1924276.001]
  • [Cites] Int J Dermatol. 1991 Dec;30(12):851-6 [1816127.001]
  • [Cites] J Laryngol Otol. 1992 Apr;106(4):368-9 [1613355.001]
  • [Cites] Head Neck. 1992 Jan-Feb;14(1):1-7 [1624288.001]
  • [Cites] Ann Otol Rhinol Laryngol. 1992 Jul;101(7):623-5 [1626913.001]
  • [Cites] Eur Arch Otorhinolaryngol. 1992;249(4):195-200 [1642875.001]
  • [Cites] J Otolaryngol. 1992 Aug;21(4):235-7 [1527824.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 1993 Sep;119(9):973-8 [8357598.001]
  • [Cites] Am J Surg Pathol. 1994 Jan;18(1):62-73 [8279629.001]
  • [Cites] Otolaryngol Head Neck Surg. 1995 Jun;112(6):735-7 [7777360.001]
  • [Cites] Cancer. 1996 Jun 1;77(11):2400-6 [8635113.001]
  • [Cites] Histopathology. 1996 Mar;28(3):235-40 [8729042.001]
  • [Cites] Am J Surg Pathol. 1997 Apr;21(4):363-74 [9130982.001]
  • [Cites] Ann Otol Rhinol Laryngol. 1997 Nov;106(11):943-51 [9373085.001]
  • [Cites] J Histochem Cytochem. 1998 Feb;46(2):165-76 [9446823.001]
  • [Cites] Am J Surg Pathol. 1998 Feb;22(2):246-50 [9500227.001]
  • [Cites] J Am Acad Dermatol. 1998 May;38(5 Pt 2):837-40 [9591798.001]
  • [Cites] J Laryngol Otol. 1998 Mar;112(3):280-2 [9624380.001]
  • [Cites] Gac Med Mex. 2006 Mar-Apr;142(2):155-8 [16711550.001]
  • [Cites] Arch Pathol Lab Med. 2007 Feb;131(2):288-92 [17284115.001]
  • [Cites] Cancer. 1979 Sep;44(3):1106-13 [573173.001]
  • [Cites] Head Neck Surg. 1979 Jan-Feb;1(3):274-80 [574132.001]
  • [Cites] Am J Surg Pathol. 1980 Oct;4(5):470-9 [7435775.001]
  • [Cites] Head Neck Surg. 1981 Mar-Apr;3(4):326-39 [6260710.001]
  • [Cites] Cancer. 1981 Oct 15;48(8):1907-21 [7197190.001]
  • [Cites] Am J Otolaryngol. 1999 Jul-Aug;20(4):223-31 [10442774.001]
  • [Cites] Surg Gynecol Obstet. 1950 Oct;91(4):465-82 [14782142.001]
  • [Cites] Jibiinkoka. 1963 Nov;35:943-5 [14096917.001]
  • [Cites] Ear Nose Throat J. 2005 Jan;84(1):45-6, 51 [15742774.001]
  • [Cites] Otolaryngol Pol. 2005;59(1):105-8 [15915928.001]
  • [Cites] Otolaryngol Head Neck Surg. 2006 May;134(5):886-7 [16647554.001]
  • [Cites] Am J Surg Pathol. 1998 Jun;22(6):683-97 [9630175.001]
  • [Cites] Lin Chuang Er Bi Yan Hou Ke Za Zhi. 1997 Feb;11(2):64-5 [9644183.001]
  • [Cites] J Laryngol Otol. 1998 May;112(5):500-2 [9747488.001]
  • [Cites] Neurosurgery. 1999 Feb;44(2):405-7; discussion 407-8 [9932897.001]
  • [Cites] J Oral Pathol Med. 1999 Feb;28(2):92-5 [9950257.001]
  • [Cites] Virchows Arch. 1999 Jan;434(1):51-6 [10071235.001]
  • [Cites] Am J Surg. 1973 Oct;126(4):547-56 [4355257.001]
  • [Cites] Cancer. 1974 May;33(5):1275-88 [4362952.001]
  • [Cites] Cancer. 1976 Sep;38(3):1227-36 [986234.001]
  • [Cites] J Oral Surg. 1976 Nov;34(11):1019-21 [1068252.001]
  • [Cites] Clin Exp Dermatol. 1976 Dec;1(4):287-312 [793743.001]
  • [Cites] J Laryngol Otol. 1979 Feb;93(2):181-6 [571001.001]
  • [Cites] Cancer Genet Cytogenet. 2001 Aug;129(1):64-8 [11520569.001]
  • [Cites] Laryngoscope. 2001 Jul;111(7):1197-202 [11568541.001]
  • [Cites] Acta Otorhinolaryngol Belg. 2001;55(3):241-6 [11685962.001]
  • [Cites] Mod Pathol. 2002 Mar;15(3):324-30 [11904345.001]
  • [Cites] Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2002 Sep;94(3):333-7 [12324789.001]
  • [Cites] Am J Surg Pathol. 2002 Oct;26(10):1319-29 [12360047.001]
  • [Cites] J Dermatol. 2002 Sep;29(9):593-8 [12392068.001]
  • [Cites] Int J Surg Pathol. 2001 Oct;9(4):309-15 [12574849.001]
  • [Cites] J Laryngol Otol. 2003 Jan;117(1):75-7 [12590863.001]
  • [Cites] Mod Pathol. 2003 Mar;16(3):263-71 [12640107.001]
  • [Cites] Am J Surg Pathol. 2003 May;27(5):594-611 [12717245.001]
  • [Cites] Am J Surg Pathol. 2003 Jun;27(6):737-49 [12766577.001]
  • [Cites] Ear Nose Throat J. 2003 Aug;82(8):608-10, 612, 614 [14503098.001]
  • [Cites] Am J Surg Pathol. 2004 Apr;28(4):505-13 [15087670.001]
  • [Cites] Am J Surg. 1968 Oct;116(4):548-53 [5692131.001]
  • [Cites] Rev Stomatoodontol Nord Fr. 1968 Oct-Dec;23(91):159-72 [5751937.001]
  • [Cites] Cancer. 1970 Oct;26(4):868-83 [5528267.001]
  • [Cites] Acta Otolaryngol Suppl. 1971;289:1-25 [4338000.001]
  • [Cites] ORL J Otorhinolaryngol Relat Spec. 1982;44(6):335-9 [6292811.001]
  • [Cites] Clin Exp Dermatol. 1984 May;9(3):232-42 [6539660.001]
  • [Cites] J Endod. 1983 Feb;9(2):65-70 [6590766.001]
  • [Cites] Head Neck Surg. 1981 Jan-Feb;3(3):231-9 [7461981.001]
  • [Cites] J Cutan Pathol. 1985 Feb;12(1):66-71 [4038718.001]
  • [Cites] J Am Acad Dermatol. 1985 May;12(5 Pt 1):781-96 [4008683.001]
  • [Cites] Otolaryngol Head Neck Surg. 1985 Jun;93(3):436-41 [3927245.001]
  • [Cites] Eur J Surg Oncol. 1986 Jun;12(2):147-52 [3709819.001]
  • [Cites] Br J Oral Maxillofac Surg. 1986 Aug;24(4):286-92 [2942183.001]
  • [Cites] Laryngoscope. 1986 Dec;96(12):1321-9 [3023771.001]
  • [Cites] Laryngoscope. 1986 Dec;96(12):1381-4 [3784742.001]
  • [Cites] Cancer. 1987 Mar 1;59(5):1046-57 [3815265.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 1987 Sep;113(9):936-42 [3038146.001]
  • [Cites] Acta Otolaryngol. 1988 Jan-Feb;105(1-2):132-9 [2829500.001]
  • [Cites] J Laryngol Otol. 1988 May;102(5):464-7 [3294314.001]
  • [Cites] J Laryngol Otol. 1988 Dec;102(12):1159-60 [3066836.001]
  • [Cites] J Oral Maxillofac Surg. 1989 Jul;47(7):747-53 [2659753.001]
  • [Cites] Hum Pathol. 2000 Feb;31(2):239-41 [10685640.001]
  • [Cites] J Laryngol Otol. 2000 May;114(5):381-4 [10912272.001]
  • [Cites] Hum Pathol. 2000 Sep;31(9):1062-7 [11014572.001]
  • [Cites] Eur J Dermatol. 2000 Oct-Nov;10(7):555-8 [11056431.001]
  • [Cites] J Laryngol Otol. 1989 Sep;103(9):874-6 [2685156.001]
  • (PMID = 20614274.001).
  • [ISSN] 1936-0568
  • [Journal-full-title] Head and neck pathology
  • [ISO-abbreviation] Head Neck Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  • [Other-IDs] NLM/ PMC2807511
  • [Keywords] NOTNLM ; Angiosarcoma / Differential diagnosis / Hemangioma / Immunohistochemistry / Nasal cavity / Prognosis / Sarcoma / Sinonasal tract / Survival / Vascular
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99. Patton KT, Deyrup AT, Weiss SW: Atypical vascular lesions after surgery and radiation of the breast: a clinicopathologic study of 32 cases analyzing histologic heterogeneity and association with angiosarcoma. Am J Surg Pathol; 2008 Jun;32(6):943-50
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Atypical vascular lesions after surgery and radiation of the breast: a clinicopathologic study of 32 cases analyzing histologic heterogeneity and association with angiosarcoma.
  • Of the 21 patients, 17 are alive without disease, 1 is alive with disease, 1 died of breast carcinoma, 1 died of unknown causes, and 1 showed progressive histologic changes in the AVLs over a period of 5 years resulting in a well-differentiated angiosarcoma.
  • One patient underwent a mastectomy that revealed extensive residual AVL and the second developed a high-grade angiosarcoma after 14 months.
  • There seems to be an association of AVL with angiosarcoma that differs depending on the histologic features, with the VT AVLs having the higher risk.
  • In the 2 patients who developed angiosarcoma, morphologic evidence suggested AVLs to be a precursor rather than simply a risk factor.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology. Neoplasms, Radiation-Induced / pathology
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Female. Humans. Mastectomy, Segmental. Middle Aged

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  • (PMID = 18551753.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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100. Quesenberry CD, Li C, Chen AH, Zweizig SL, Ball HG 3rd: Primary angiosarcoma of the ovary: a case report of Stage I disease. Gynecol Oncol; 2005 Oct;99(1):218-21
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the ovary: a case report of Stage I disease.
  • BACKGROUND: There are 20 documented cases of primary ovarian angiosarcoma.
  • CASE: We present a case of Stage Ic primary ovarian angiosarcoma treated with 3 cycles of adjuvant MAID chemotherapy.
  • CONCLUSION: A review of the literature indicates a potential role for MAID chemotherapy in the treatment of ovarian angiosarcomas.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Hemangiosarcoma / drug therapy. Ovarian Neoplasms / drug therapy
  • [MeSH-minor] Adult. Chemotherapy, Adjuvant. Dacarbazine / administration & dosage. Doxorubicin / administration & dosage. Female. Humans. Ifosfamide / administration & dosage. Mesna / administration & dosage. Neoplasm Staging

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  • (PMID = 16081151.001).
  • [ISSN] 0090-8258
  • [Journal-full-title] Gynecologic oncology
  • [ISO-abbreviation] Gynecol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 7GR28W0FJI / Dacarbazine; 80168379AG / Doxorubicin; NR7O1405Q9 / Mesna; UM20QQM95Y / Ifosfamide; MAID protocol
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