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1. Obenauer S, Sohns C, Werner C, Grabbe E: Computer-aided detection in full-field digital mammography: detection in dependence of the BI-RADS categories. Breast J; 2006 Jan-Feb;12(1):16-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Adenocarcinoma / pathology. Adenocarcinoma / radiography. Adenocarcinoma, Mucinous / pathology. Adenocarcinoma, Mucinous / radiography. Adult. Aged. Carcinoma, Ductal, Breast / pathology. Carcinoma, Ductal, Breast / radiography. Carcinoma, Intraductal, Noninfiltrating / pathology. Carcinoma, Intraductal, Noninfiltrating / radiography. Carcinoma, Lobular / pathology. Carcinoma, Lobular / radiography. Carcinoma, Medullary / pathology. Carcinoma, Medullary / radiography. Carcinoma, Papillary / pathology. Carcinoma, Papillary / radiography. False Positive Reactions. Female. Hemangiosarcoma / pathology. Hemangiosarcoma / radiography. Humans. Middle Aged. Predictive Value of Tests. Retrospective Studies. Sensitivity and Specificity

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  • (PMID = 16409582.001).
  • [ISSN] 1075-122X
  • [Journal-full-title] The breast journal
  • [ISO-abbreviation] Breast J
  • [Language] eng
  • [Publication-type] Evaluation Studies; Journal Article
  • [Publication-country] United States
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2. Sher T, Hennessy BT, Valero V, Broglio K, Woodward WA, Trent J, Hunt KK, Hortobagyi GN, Gonzalez-Angulo AM: Primary angiosarcomas of the breast. Cancer; 2007 Jul 1;110(1):173-8
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  • [Title] Primary angiosarcomas of the breast.
  • BACKGROUND: The purpose of the study was to describe the clinicopathologic characteristics and clinical outcomes of patients with primary breast angiosarcoma.
  • METHODS: The institutional database was searched to identify breast angiosarcoma patients seen between 1965 and 2002.
  • CONCLUSIONS: Breast angiosarcoma is frequently advanced at diagnosis and has a tendency for local-regional recurrence.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology
  • [MeSH-minor] Adolescent. Adult. Aged. Aged, 80 and over. Female. Follow-Up Studies. Humans. Lymphatic Metastasis. Middle Aged. Neoplasm Staging. Receptors, Estrogen / metabolism. Receptors, Progesterone / metabolism. Survival Analysis

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  • [Copyright] Copyright (c) 2007 American Cancer Society.
  • (PMID = 17541936.001).
  • [ISSN] 0008-543X
  • [Journal-full-title] Cancer
  • [ISO-abbreviation] Cancer
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / L30 CA123630; United States / NCI NIH HHS / CA / L30 CA123630-01; United States / NCI NIH HHS / CA / L30 CA123630-02
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Receptors, Estrogen; 0 / Receptors, Progesterone
  • [Other-IDs] NLM/ NIHMS283619; NLM/ PMC4329779
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3. 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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4. Rossi G, Sartori G, Valli R, Bertolini F, Bigiani N, Schirosi L, Cavazza A, Luppi G: The value of c-kit mutational analysis in a cytokeratin positive gastrointestinal stromal tumour. J Clin Pathol; 2005 Sep;58(9):991-3
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  • This report describes a metastatic GIST that stained strongly for cytokeratins, CD117, and CD34 in a patient who was previously diagnosed with gastric epithelioid angiosarcoma.
  • [MeSH-minor] Adult. Biomarkers, Tumor / metabolism. Diagnosis, Differential. Female. Hemangiosarcoma / diagnosis. Humans. Pelvic Neoplasms / diagnosis. Pelvic Neoplasms / secondary

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  • (PMID = 16126886.001).
  • [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
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 68238-35-7 / Keratins; EC 2.7.10.1 / Proto-Oncogene Proteins c-kit
  • [Other-IDs] NLM/ PMC1770815
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5. Berry MF, Williams M, Welsby I, Lin S: Cardiac angiosarcoma presenting with right coronary artery pseudoaneurysm. J Cardiothorac Vasc Anesth; 2010 Aug;24(4):633-5
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  • [Title] Cardiac angiosarcoma presenting with right coronary artery pseudoaneurysm.
  • [MeSH-major] Aneurysm, False / diagnosis. Coronary Vessels / pathology. Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Diagnosis, Differential. Humans. Male

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  • (PMID = 19525126.001).
  • [ISSN] 1532-8422
  • [Journal-full-title] Journal of cardiothoracic and vascular anesthesia
  • [ISO-abbreviation] J. Cardiothorac. Vasc. Anesth.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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6. O'Donnell ME, Scally N, Carson J, Kenny B, Whiteside MC: Angiosarcoma: a difficult diagnosis. Hosp Med; 2005 Jul;66(7):428-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma: a difficult diagnosis.
  • [MeSH-major] Breast / pathology. Breast Neoplasms / pathology. Hemangiosarcoma / pathology
  • [MeSH-minor] Adult. Biopsy, Needle. Diagnosis, Differential. Female. Humans. Mammography / methods

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  • (PMID = 16025806.001).
  • [ISSN] 1462-3935
  • [Journal-full-title] Hospital medicine (London, England : 1998)
  • [ISO-abbreviation] Hosp Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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7. 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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  • (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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8. 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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  • (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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9. Salas S, Stock N, Stoeckle E, Kind M, Bui B, Coindre JM: Chronic lymphedema due to morbid obesity: an exceptional cause of abdominal wall angiosarcoma. Virchows Arch; 2008 Aug;453(2):217-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Chronic lymphedema due to morbid obesity: an exceptional cause of abdominal wall angiosarcoma.
  • [MeSH-major] Abdominal Wall / pathology. Hemangiosarcoma / etiology. Lymphedema / etiology. Obesity, Morbid / complications
  • [MeSH-minor] Adult. Fatal Outcome. Humans. Male. Skin Neoplasms / etiology. Skin Neoplasms / pathology

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  • (PMID = 18560886.001).
  • [ISSN] 0945-6317
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Germany
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10. 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
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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 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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11. Ceyhan K, Percinel S, Kinkli G, Karaca E, Umudum H: Epithelioid angiosarcoma. Acta Cytol; 2010 Jan-Feb;54(1):109-12
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Epithelioid angiosarcoma.
  • [MeSH-major] Hemangiosarcoma / pathology. Liver Neoplasms / pathology
  • [MeSH-minor] Adult. Biopsy, Fine-Needle. Humans. Immunohistochemistry. Male

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  • (PMID = 20307003.001).
  • [ISSN] 0001-5547
  • [Journal-full-title] Acta cytologica
  • [ISO-abbreviation] Acta Cytol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] United States
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12. 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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  • [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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13. 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
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  • [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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14. Di Matteo FM, De Stefano M, Vanni B, Palermo S, Biancafarina A, Giusti D, Savino G, Di Marco C, Casalvieri L, De Antoni E: [Retroperitoneal giant mixed sarcoma. Case report]. G Chir; 2008 May;29(5):238-41
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  • [Title] [Retroperitoneal giant mixed sarcoma. Case report].
  • [Transliterated title] Un caso di sarcoma misto retroperitoneale gigante.
  • Histology showed a mixed liposarcoma and angiosarcoma with high grade of malignancy and positivity for vimentin, factor VIII, CD34, CD31 and negativity for S-100, CD68, AMS, AML.
  • [MeSH-major] Hemangiosarcoma / surgery. Liposarcoma / surgery. Neoplasms, Multiple Primary / surgery. Retroperitoneal Neoplasms / surgery
  • [MeSH-minor] Adult. Female. Humans. Prognosis. Treatment Outcome

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  • (PMID = 18507961.001).
  • [ISSN] 0391-9005
  • [Journal-full-title] Il Giornale di chirurgia
  • [ISO-abbreviation] G Chir
  • [Language] ita
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Italy
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15. 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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16. 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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  • [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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17. 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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18. Abedalthagafi M, Rushing EJ, Auerbach A, Desouki MM, Marwaha J, Wang Z, Fanburg-Smith JC: Sporadic cutaneous angiosarcomas generally lack hypoxia-inducible factor 1alpha: a histologic and immunohistochemical study of 45 cases. Ann Diagn Pathol; 2010 Feb;14(1):15-22
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  • [Title] Sporadic cutaneous angiosarcomas generally lack hypoxia-inducible factor 1alpha: a histologic and immunohistochemical study of 45 cases.
  • Cutaneous angiosarcoma (AS) is a rare malignant neoplasm of dermis composed of infiltrating cells of endothelial phenotype with overall poor prognosis.
  • Although autocrine stimulation by vascular endothelial growth factor secretion may play a role in the pathogenesis of angiosarcoma, its mechanism has not been fully established.
  • The stability of HIF can regulate key proteins in angiogenesis and the alpha-subunit has been found in epithelial tumors, only 1 case of human retroperitoneal angiosarcoma, and rare vascular proliferations and tumors in knockout mice.
  • Cases coded as "angiosarcoma" of dermis were culled and re-reviewed for inclusion as AS, based on patient folder, slides, and obtained immunohistochemistry including CD31 and smooth muscle actin (SMA).
  • There was no history of other primary, lymphedema, radiation, breast-associated, or thorotrast-induced angiosarcoma.
  • Cutaneous angiosarcoma is largely found on the scalp of older individuals.
  • Cutaneous angiosarcoma generally lacks HIF-1alpha expression.
  • [MeSH-major] Dermis / metabolism. Hemangiosarcoma / metabolism. Hypoxia-Inducible Factor 1, alpha Subunit / metabolism. Neovascularization, Pathologic / metabolism. Skin Neoplasms / metabolism
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Anoxia / metabolism. Anoxia / pathology. Female. Follow-Up Studies. Humans. Immunohistochemistry. Male. Middle Aged. Neoplasm Recurrence, Local / metabolism. Neoplasm Recurrence, Local / mortality. Neoplasm Recurrence, Local / pathology

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  • [Copyright] Published by Elsevier Inc.
  • (PMID = 20123452.001).
  • [ISSN] 1532-8198
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / HIF1A protein, human; 0 / Hypoxia-Inducible Factor 1, alpha Subunit
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19. 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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20. Vijayalakshmi SP, Arunharke M, Sundaram: Erythematous plaque over the face. Indian J Dermatol Venereol Leprol; 2006 Nov-Dec;72(6):471-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Facial Neoplasms / pathology. Hemangiosarcoma / pathology. Skin Neoplasms / pathology
  • [MeSH-minor] Adult. Antigens, CD34 / metabolism. Humans. Immunohistochemistry. Male. Mitosis

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  • (PMID = 17179632.001).
  • [ISSN] 0973-3922
  • [Journal-full-title] Indian journal of dermatology, venereology and leprology
  • [ISO-abbreviation] Indian J Dermatol Venereol Leprol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
  • [Chemical-registry-number] 0 / Antigens, CD34
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21. Wang J, Li Q, Sun Y, Cui YL: [A case of angiosarcoma developed from liver hamartomas]. Zhonghua Gan Zang Bing Za Zhi; 2006 Sep;14(9):717
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  • [Title] [A case of angiosarcoma developed from liver hamartomas].
  • [MeSH-major] Hamartoma / pathology. Hemangiosarcoma / pathology. Liver Neoplasms / pathology
  • [MeSH-minor] Adult. Female. Humans

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  • (PMID = 16996000.001).
  • [ISSN] 1007-3418
  • [Journal-full-title] Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology
  • [ISO-abbreviation] Zhonghua Gan Zang Bing Za Zhi
  • [Language] chi
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] China
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22. Wan Musa WR, Abdulwakil Elraied MA, Phang KS, Kwah YG, Tan SP, Harun R, Ban AY: Primary epithelioid angiosarcoma of the lung presenting as left-sided shoulder pain. Ann Acad Med Singapore; 2010 Aug;39(8):658-9
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  • [Title] Primary epithelioid angiosarcoma of the lung presenting as left-sided shoulder pain.
  • [MeSH-major] Hemangiosarcoma / complications. Lung Neoplasms / complications. Sarcoma / complications. Shoulder Pain / diagnosis
  • [MeSH-minor] Humans. Male. Young Adult

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  • (PMID = 20838710.001).
  • [ISSN] 0304-4602
  • [Journal-full-title] Annals of the Academy of Medicine, Singapore
  • [ISO-abbreviation] Ann. Acad. Med. Singap.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Singapore
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23. Requena Caballero C, Nicolau MJ, Haro R, Martorell A, Sanmartín O, Llombart B, Botella R, Guillén C, Requena L: [Proliferative cutaneous epithelioid angiomatous nodule]. Actas Dermosifiliogr; 2009 Mar;100(2):137-41
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Adult. Angiomatosis, Bacillary / diagnosis. Diagnosis, Differential. Female. Hemangioendothelioma, Epithelioid / diagnosis. Hemangiosarcoma / diagnosis. Humans. Male. Pregnancy. Shoulder

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  • (PMID = 19445879.001).
  • [ISSN] 0001-7310
  • [Journal-full-title] Actas dermo-sifiliográficas
  • [ISO-abbreviation] Actas Dermosifiliogr
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 10
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24. 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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  • [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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25. 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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  • [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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26. Altan E, Arslan C, Dede D, Dogan E, Altundag K: Primary angiosarcoma of the breast after pregnancy. Am Surg; 2010 Aug;76(8):E115
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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 after pregnancy.
  • [MeSH-major] Breast Neoplasms. Hemangiosarcoma
  • [MeSH-minor] Adult. Biopsy. Diagnosis, Differential. Female. Humans. Mastectomy. Ultrasonography, Mammary

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  • (PMID = 21513627.001).
  • [ISSN] 0003-1348
  • [Journal-full-title] The American surgeon
  • [ISO-abbreviation] Am Surg
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] United States
  • [Chemical-registry-number] Angiosarcoma of the breast
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27. Weissferdt A, Kalhor N, Suster S, Moran CA: Primary angiosarcomas of the anterior mediastinum: a clinicopathologic and immunohistochemical study of 9 cases. Hum Pathol; 2010 Dec;41(12):1711-7
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  • [Title] Primary angiosarcomas of the anterior mediastinum: a clinicopathologic and immunohistochemical study of 9 cases.
  • We report 9 cases of primary angiosarcomas of the anterior mediastinum.
  • Primary angiosarcomas of the anterior mediastinum are rare tumors that need to be added to the differential diagnosis of primary anterior mediastinal neoplasms.
  • Despite their histologic similarity to angiosarcomas at other sites, primary angiosarcomas of the anterior mediastinum appear to follow a more protracted clinical course than their counterparts in other organ systems.
  • [MeSH-major] Hemangiosarcoma / pathology. Mediastinal Neoplasms / pathology. Mediastinum / pathology
  • [MeSH-minor] Adult. Biomarkers, Tumor / metabolism. Combined Modality Therapy. Disease-Free Survival. Fatal Outcome. Female. Humans. Immunohistochemistry. Male. Middle Aged. Thymus Gland / pathology

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  • [Copyright] Copyright © 2010 Elsevier Inc. All rights reserved.
  • (PMID = 20709359.001).
  • [ISSN] 1532-8392
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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28. 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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  • [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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29. Hoti E, Adam R: Liver transplantation for primary and metastatic liver cancers. Transpl Int; 2008 Dec;21(12):1107-17
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  • There is no controversy about the fact that liver transplantation for HCC in the adult population yields good results for patients whose tumour masses do not exceed the Milan criteria.
  • Epithelioid hemangioendothelioma is also an appropriate indication for liver transplantation, even in the presence of extrahepatic metastases, unlike angiosarcoma which is associated with a very poor survival and considered as a contraindication.
  • [MeSH-minor] Bile Duct Neoplasms / surgery. Carcinoma, Hepatocellular / pathology. Carcinoma, Hepatocellular / surgery. Cholangiocarcinoma / surgery. Colorectal Neoplasms / pathology. Hemangioendothelioma / surgery. Hemangiosarcoma / surgery. Humans. Neoplasm Metastasis. Neoplasm Staging. Neuroendocrine Tumors / surgery. Survival Analysis. Survivors. Treatment Outcome

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  • (PMID = 18713148.001).
  • [ISSN] 0934-0874
  • [Journal-full-title] Transplant international : official journal of the European Society for Organ Transplantation
  • [ISO-abbreviation] Transpl. Int.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 75
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30. 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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  • [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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31. 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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  • [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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32. Bien E, Kazanowska B, Dantonello T, Adamkiewicz-Drozynska E, Balcerska A, Madziara W, Rybczynska A, Nurzynska-Flak J, Solarz E, Kurylak A, Zalewska-Szewczyk B, Krawczyk M, Izycka-Swieszewska E, Rapala M, Koscielniak E: Factors predicting survival in childhood malignant and intermediate vascular tumors : retrospective analysis of the Polish and German cooperative paediatric soft tissue sarcoma study groups and review of the literature. Ann Surg Oncol; 2010 Jul;17(7):1878-89
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  • [Title] Factors predicting survival in childhood malignant and intermediate vascular tumors : retrospective analysis of the Polish and German cooperative paediatric soft tissue sarcoma study groups and review of the literature.
  • METHODS: A total of 32 children with malignant vascular tumors (14 angiosarcomas [AS], 5 epithelioid hemangioendotheliomas, and 13 intermediate vascular tumors, including other hemangioendotheliomas plus adult-type hemangiopericytomas), registered in the German and Polish Paediatric Soft Tissue Sarcomas Study Groups, were treated following the Cooperative Weichteilsarkom Studiengruppe (CWS)-81, -86, -91, and -96 protocols.
  • [MeSH-major] Hemangioendothelioma / mortality. Hemangiopericytoma / mortality. Hemangiosarcoma / mortality. Sarcoma / mortality. Vascular Neoplasms / mortality
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Germany / epidemiology. Humans. Infant. Infant, Newborn. Male. Poland / epidemiology. Retrospective Studies. Survival Rate. Young Adult

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  • (PMID = 20333551.001).
  • [ISSN] 1534-4681
  • [Journal-full-title] Annals of surgical oncology
  • [ISO-abbreviation] Ann. Surg. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study
  • [Publication-country] United States
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33. Weaver J, Billings SD: Postradiation cutaneous vascular tumors of the breast: a review. Semin Diagn Pathol; 2009 Aug;26(3):141-9
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  • (1) postradiation cutaneous angiosarcoma, malignant vascular neoplasms with significant morbidity and mortality; and (2) atypical vascular lesions (AVL), vascular tumors that reportedly behave in a benign manner.
  • Although first described separately 15 years ago, the relationship between postradiation cutaneous angiosarcoma and AVL remains controversial.
  • It appears that, in at least some cases, angiosarcoma can arise in the context of AVL, suggesting that these lesions are part of a spectrum of the same disease process.
  • Herein, we will discuss the evolution of this topic while reviewing the various clinical, histopathologic, and prognostic characteristics of postradiation cutaneous angiosarcoma and AVL.
  • [MeSH-major] Breast Neoplasms / radiotherapy. Hemangiosarcoma / pathology. Neoplasms, Radiation-Induced / pathology. Skin Neoplasms / pathology
  • [MeSH-minor] Adult. Aged. Female. Humans. Middle Aged. Neoplasm Recurrence, Local. Prognosis

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  • (PMID = 20043513.001).
  • [ISSN] 0740-2570
  • [Journal-full-title] Seminars in diagnostic pathology
  • [ISO-abbreviation] Semin Diagn Pathol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 21
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34. Sheu SY, Grabellus F, Schwertheim S, Mann K, Ensinger C, Ofner D, Bockhorn M, Fuhrer D, Schmid KW: COX-2 expression in highly aggressive thyroid malignancies - indication for a possible therapeutic option? Horm Metab Res; 2009 Apr;41(4):314-9
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  • Both anaplastic thyroid carcinoma (ATC) and angiosarcoma of the thyroid (AST) are highly aggressive malignancies with very limited therapeutic options.
  • [MeSH-major] Carcinoma / metabolism. Cyclooxygenase 2 / metabolism. Gene Expression. Hemangiosarcoma / metabolism. Thyroid Neoplasms / metabolism
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Female. Humans. Male. Middle Aged. Retrospective Studies

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  • (PMID = 19048457.001).
  • [ISSN] 1439-4286
  • [Journal-full-title] Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme
  • [ISO-abbreviation] Horm. Metab. Res.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] EC 1.14.99.1 / Cyclooxygenase 2; EC 1.14.99.1 / PTGS2 protein, human
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35. 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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  • [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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36. Baumhoer D, Gunawan B, Becker H, Füzesi L: Comparative genomic hybridization in four angiosarcomas of the female breast. Gynecol Oncol; 2005 May;97(2):348-52
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  • [Title] Comparative genomic hybridization in four angiosarcomas of the female breast.
  • OBJECTIVE: Angiosarcomas represent a heterogeneous group of malignant vascular tumors occurring in different anatomic sites.
  • In the female breast, they account for less than 1% of all malignant tumors and mainly develop as secondary angiosarcomas after prior irradiation.
  • Data on cytogenetic findings in angiosarcomas are scarce and up to now no characteristic primary aberrations have been established.
  • We herein add molecular cytogenetic findings in another 4 angiosarcomas to 11 previously reported cases.
  • METHODS: We investigated four angiosarcomas of the female breast (three primary angiosarcomas and one secondary tumor after irradiation for breast cancer) for DNA copy number changes using comparative genomic hybridization (CGH).
  • RESULTS: All angiosarcomas revealed aberrant karyotypes including multiple DNA copy number changes involving various chromosomes.
  • CONCLUSIONS: Angiosarcoma of the female breast represents a genetically heterogeneous tumor entity without a readily identifiable pattern of common chromosomal alterations.
  • However, reviewing the cytogenetic literature on angiosarcomas of different sites, gains at 8q and 20p appear to emerge as the most frequent aberrations in at least a subset of these tumors.
  • [MeSH-major] Breast Neoplasms / genetics. Hemangiosarcoma / genetics
  • [MeSH-minor] Adult. Female. Gene Dosage. Humans. Karyotyping. Middle Aged. Nucleic Acid Hybridization

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  • (PMID = 15863129.001).
  • [ISSN] 0090-8258
  • [Journal-full-title] Gynecologic oncology
  • [ISO-abbreviation] Gynecol. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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37. 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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  • [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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38. Moses KA, Tillett JW, Master VA: Primary penile angiosarcoma in a patient with AIDS: a case report. AIDS; 2007 Nov 12;21(17):2355-6
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  • [Title] Primary penile angiosarcoma in a patient with AIDS: a case report.
  • [MeSH-major] Acquired Immunodeficiency Syndrome / complications. Hemangiosarcoma / virology. Penile Neoplasms / virology
  • [MeSH-minor] Adult. Humans. Male. Sarcoma, Kaposi / complications

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  • (PMID = 18090289.001).
  • [ISSN] 0269-9370
  • [Journal-full-title] AIDS (London, England)
  • [ISO-abbreviation] AIDS
  • [Language] eng
  • [Publication-type] Case Reports; Letter; Review
  • [Publication-country] England
  • [Number-of-references] 11
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39. McMahon GS, Mikhail HM, Molyneux AJ, Thomas DV, Hicks RC: "Masson's pseudoangiosarcoma" in a popliteal aneurysm: tumor or thrombus? Cause or effect? Ann Vasc Surg; 2010 Feb;24(2):257.e1-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Aneurysm / complications. Endothelium, Vascular / pathology. Hemangiosarcoma / complications. Popliteal Artery / pathology. Thrombosis / complications. Vascular Neoplasms / complications
  • [MeSH-minor] Adult. Embolism / etiology. Embolism / therapy. Humans. Hyperplasia. Male. Saphenous Vein / transplantation. Thrombolytic Therapy. Tibial Arteries / surgery. Treatment Outcome. Vascular Surgical Procedures

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  • [Copyright] Copyright 2009 Annals of Vascular Surgery Inc. Published by Elsevier Inc. All rights reserved.
  • (PMID = 19892519.001).
  • [ISSN] 1615-5947
  • [Journal-full-title] Annals of vascular surgery
  • [ISO-abbreviation] Ann Vasc Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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40. Lvoff NM, Leung JW: Case of the season: primary angiosarcoma of the breast: correlative imaging and pathology. Semin Roentgenol; 2007 Oct;42(4):208-10
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  • [Title] Case of the season: primary angiosarcoma of the breast: correlative imaging and pathology.
  • [MeSH-major] Breast Neoplasms / diagnosis. Diagnostic Imaging. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Contrast Media. Diagnosis, Differential. Female. Humans. Mastectomy, Radical

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  • (PMID = 17919522.001).
  • [ISSN] 0037-198X
  • [Journal-full-title] Seminars in roentgenology
  • [ISO-abbreviation] Semin Roentgenol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Contrast Media
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41. Sheehan M, Roumpf SO, Summerlin DJ, Billings SD: Spindle cell hemangioma: report of a case presenting in the oral cavity. J Cutan Pathol; 2007 Oct;34(10):797-800
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Adult. Biomarkers, Tumor / metabolism. Diagnosis, Differential. Hemangioendothelioma, Epithelioid / diagnosis. Hemangiosarcoma / diagnosis. Humans. Male. Sarcoma, Kaposi / diagnosis. Treatment Outcome

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  • (PMID = 17880587.001).
  • [ISSN] 0303-6987
  • [Journal-full-title] Journal of cutaneous pathology
  • [ISO-abbreviation] J. Cutan. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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42. Serrano C, García Á, Brana I, Pérez-Benavente A, Oaknin A: Angiosarcoma of the ovary: is it always a lethal disease? J Clin Oncol; 2010 Nov 20;28(33):e675-7
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  • [Title] Angiosarcoma of the ovary: is it always a lethal disease?
  • [MeSH-major] Hemangiosarcoma / diagnosis. Ovarian Neoplasms / diagnosis
  • [MeSH-minor] Female. Humans. Young Adult

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  • (PMID = 20823420.001).
  • [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] Case Reports; Journal Article
  • [Publication-country] United States
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43. Mayer F, Aebert H, Rudert M, Königsrainer A, Horger M, Kanz L, Bamberg M, Ziemer G, Hartmann JT: Primary malignant sarcomas of the heart and great vessels in adult patients--a single-center experience. Oncologist; 2007 Sep;12(9):1134-42
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  • [Title] Primary malignant sarcomas of the heart and great vessels in adult patients--a single-center experience.
  • BACKGROUND: Sarcomas arising in the heart or the great vessels are rare entities.
  • METHODS: Between January 1993 and September 2006, of 1,429 patients registered to the Sarcoma Center, 14 had a primary sarcoma of the heart or large vessels.
  • The most frequently encountered histologic subtypes were leiomyosarcoma and angiosarcoma.
  • CONCLUSIONS: Patients with primary sarcomas of the heart and the large vessels were of a young age, and more than half of them presented with advanced disease.
  • [MeSH-major] Heart Neoplasms / epidemiology. Sarcoma / epidemiology. Vascular Neoplasms / epidemiology
  • [MeSH-minor] Adult. Aortic Diseases / epidemiology. Female. Follow-Up Studies. Germany / epidemiology. Hemangiosarcoma / epidemiology. Humans. Leiomyosarcoma / epidemiology. Lung Neoplasms / secondary. Lymphatic Metastasis. Male. Middle Aged. Neoadjuvant Therapy / statistics & numerical data. Pulmonary Artery / pathology. Remission Induction. Retrospective Studies. Survival Rate. Venae Cavae / pathology

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  • (PMID = 17914083.001).
  • [ISSN] 1083-7159
  • [Journal-full-title] The oncologist
  • [ISO-abbreviation] Oncologist
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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44. Gagua PO, Macharashvili LI, Kuchava VO, Gzirishvili LM, Lomidze ZT: [Diagnosis and results of surgical treatment of rare giant intrathoracic tumors]. Khirurgiia (Mosk); 2005;(12):21-4
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  • Sarcoma was diagnosed in 10 patients, mesenchymal tumors -- in 4, neurogenic tumors -- in 3, thymoma -- in 2 patients.
  • [MeSH-major] Hemangiosarcoma / radiography. Hemangiosarcoma / surgery. Liposarcoma / radiography. Liposarcoma / surgery. Thoracic Neoplasms / radiography. Thoracic Neoplasms / surgery. Thoracic Surgical Procedures / methods
  • [MeSH-minor] Adult. Female. Humans. Male. Middle Aged. Neoplasm Invasiveness. Neoplasm Staging. Tomography, X-Ray Computed

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  • (PMID = 16353021.001).
  • [ISSN] 0023-1207
  • [Journal-full-title] Khirurgiia
  • [ISO-abbreviation] Khirurgiia (Mosk)
  • [Language] rus
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
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45. Yang XH, Wu QL, Yu XB, Xu CX, Ma BF, Zhang XM, Li SN, Lahn BT, Xiang AP: Nestin expression in different tumours and its relevance to malignant grade. J Clin Pathol; 2008 Apr;61(4):467-73
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  • RESULTS: Nestin was expressed predominantly in the cytoplasm of angiosarcoma, pancreatic adenocarcinoma and GIST samples, and some tumour cells expressed in the nucleus.
  • There was a statistically significant difference between the histoscore of nestin in high malignant GIST (2.2366 (0.6920)) and that in low malignant GIST (1.3783 (0.4268)) (p = 0.003); and also between that in high malignant angiosarcoma (1.9188 (0.2069)) and that in low malignant angiosarcoma (0.6474 (0.3273)) (p = 0.000).
  • CONCLUSIONS: Results suggest that the expression of nestin may play an important role in the development of some neoplasms such as GIST and angiosarcoma.
  • [MeSH-minor] Adenocarcinoma / metabolism. Adenocarcinoma / pathology. Adult. Aged. Female. Gastrointestinal Stromal Tumors / metabolism. Gastrointestinal Stromal Tumors / pathology. Hemangiosarcoma / metabolism. Hemangiosarcoma / pathology. Humans. Immunoenzyme Techniques. Male. Middle Aged. Nestin. Pancreatic Neoplasms / metabolism. Pancreatic Neoplasms / pathology

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  • (PMID = 17873113.001).
  • [ISSN] 1472-4146
  • [Journal-full-title] Journal of clinical pathology
  • [ISO-abbreviation] J. Clin. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Intermediate Filament Proteins; 0 / NES protein, human; 0 / Neoplasm Proteins; 0 / Nerve Tissue Proteins; 0 / Nestin
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46. 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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  • [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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47. Pinto DS, Blair BM, Schwartzstein RM, Smith CC: Clinical problem-solving. A sailor's heartbreak. N Engl J Med; 2005 Sep 1;353(9):934-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Ascites / etiology. Diagnosis, Differential. Dyspnea / etiology. Echocardiography, Doppler, Color. Echocardiography, Transesophageal. Edema / etiology. Fatal Outcome. Heart Atria / pathology. Humans. Lung / radiography. Male. Pericardial Effusion / etiology. Pericardium / pathology. Pulmonary Embolism / complications. Pulmonary Embolism / diagnosis. Vomiting / etiology

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  • [CommentIn] N Engl J Med. 2005 Dec 1;353(22):2408-9; author reply 2408-9 [16319394.001]
  • (PMID = 16135839.001).
  • [ISSN] 1533-4406
  • [Journal-full-title] The New England journal of medicine
  • [ISO-abbreviation] N. Engl. J. Med.
  • [Language] eng
  • [Grant] United States / NIAID NIH HHS / AI / T32 AI007061
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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48. Gladdy RA, Qin LX, Moraco N, Edgar MA, Antonescu CR, Alektiar KM, Brennan MF, Singer S: Do radiation-associated soft tissue sarcomas have the same prognosis as sporadic soft tissue sarcomas? J Clin Oncol; 2010 Apr 20;28(12):2064-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Do radiation-associated soft tissue sarcomas have the same prognosis as sporadic soft tissue sarcomas?
  • PURPOSE To determine the prognostic significance of histologic type in radiation-associated soft tissue sarcomas (RASs) and determine whether RASs are associated with an inferior prognosis compared with sporadic soft tissue sarcomas (STSs).
  • Multivariate analysis of clinicopathologic factors for disease-specific survival (DSS) was performed for RASs, and a multivariate analysis of radiation exposure was also performed for RASs and sporadic sarcomas.
  • DSS in patients with primary RAS is significantly worse compared with sporadic STS independent of sarcoma histologic type.


49. Krombach GA, Spuentrup E, Buecker A, Mahnken AH, Katoh M, Temur Y, Higgins CB, Günther RW: [Heart tumors: magnetic resonance imaging and multislice spiral CT]. Rofo; 2005 Sep;177(9):1205-18
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Fibroma / diagnosis. Heart Neoplasms / diagnosis. Hemangioma / diagnosis. Hemangiosarcoma / diagnosis. Lipoma / diagnosis. Magnetic Resonance Imaging / methods. Myxoma / diagnosis. Pheochromocytoma / diagnosis. Rhabdomyoma / diagnosis. Tomography, Spiral Computed / methods
  • [MeSH-minor] Adult. Aged. Child. Contrast Media. Diagnosis, Differential. Echo-Planar Imaging / methods. Electrocardiography. Female. Gadolinium DTPA. Heart Atria. Heart Diseases / diagnosis. Heart Diseases / radiography. Heart Valves. Heart Ventricles. Humans. Magnetic Resonance Imaging, Cine / methods. Male. Middle Aged. Prognosis. Thrombosis / diagnosis. Thrombosis / radiography

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  • (PMID = 16123866.001).
  • [ISSN] 1438-9029
  • [Journal-full-title] RöFo : Fortschritte auf dem Gebiete der Röntgenstrahlen und der Nuklearmedizin
  • [ISO-abbreviation] Rofo
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Contrast Media; K2I13DR72L / Gadolinium DTPA
  • [Number-of-references] 59
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50. Brinckman SL, van der Wouw P: Images in cardiovascular medicine. Angiosarcoma of the pericardium: a fatal disease. Circulation; 2005 Jun 14;111(23):e388-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Images in cardiovascular medicine. Angiosarcoma of the pericardium: a fatal disease.
  • [MeSH-major] Heart Neoplasms / pathology. Hemangiosarcoma / pathology. Pericardium / pathology
  • [MeSH-minor] Adult. Echocardiography. Heart Ventricles / pathology. Heart Ventricles / ultrasonography. Humans. Magnetic Resonance Imaging. Male

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  • (PMID = 15956142.001).
  • [ISSN] 1524-4539
  • [Journal-full-title] Circulation
  • [ISO-abbreviation] Circulation
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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51. Stacher E, Gruber-Mösenbacher U, Halbwedl I, Dei Tos AP, Cavazza A, Papotti M, Carvalho L, Huber M, Ermert L, Popper HH: The VEGF-system in primary pulmonary angiosarcomas and haemangioendotheliomas: new potential therapeutic targets? Lung Cancer; 2009 Jul;65(1):49-55
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The VEGF-system in primary pulmonary angiosarcomas and haemangioendotheliomas: new potential therapeutic targets?
  • Malignant epitheloid vascular tumors (epitheloid haemangioendotheliomas and angiosarcomas) of the lung are very rare lesions often posing difficulties in diagnosis.
  • Next, we investigated several factors of the VEGF-signalling pathway as well as Tie 2 in eight primary pulmonary epitheloid haemangioendotheliomas and ten primary pulmonary epitheloid angiosarcomas by means of immunohistochemistry using commercially available antibodies against VEGF-A, VEGF-B, VEGF-C, VEGF-D, VEGFR-2, VEGFR-3 and endothelium specific kinase Tie2.
  • [MeSH-major] Hemangioendothelioma, Epithelioid / metabolism. Hemangiosarcoma / metabolism. Lung Neoplasms / metabolism. Receptors, Vascular Endothelial Growth Factor / metabolism. Vascular Endothelial Growth Factors / metabolism
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Female. Humans. Immunohistochemistry. Male. Middle Aged. Receptor, TIE-2 / metabolism. Signal Transduction

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  • (PMID = 19100646.001).
  • [ISSN] 1872-8332
  • [Journal-full-title] Lung cancer (Amsterdam, Netherlands)
  • [ISO-abbreviation] Lung Cancer
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Ireland
  • [Chemical-registry-number] 0 / Vascular Endothelial Growth Factors; EC 2.7.10.1 / Receptor, TIE-2; EC 2.7.10.1 / Receptors, Vascular Endothelial Growth Factor
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52. Yu K, Liu Y, Wang H, Hu S, Long C: Epidemiological and pathological characteristics of cardiac tumors: a clinical study of 242 cases. Interact Cardiovasc Thorac Surg; 2007 Oct;6(5):636-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Mesenchymoma and angiosarcoma were the most common primary malignant cardiac tumors.
  • [MeSH-major] Asian Continental Ancestry Group / statistics & numerical data. Heart Neoplasms. Hemangiosarcoma. Lipoma. Mesenchymoma. Myxoma. Rhabdomyoma
  • [MeSH-minor] Adolescent. Adult. Age Distribution. Aged. Child. Child, Preschool. China / epidemiology. Female. Humans. Incidence. Infant. Male. Middle Aged. Neoplasm Metastasis. Prevalence. Retrospective Studies. Sex Distribution

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  • (PMID = 17670730.001).
  • [ISSN] 1569-9285
  • [Journal-full-title] Interactive cardiovascular and thoracic surgery
  • [ISO-abbreviation] Interact Cardiovasc Thorac Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
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53. 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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54. Akiyama T, Hamazaki S, Monobe Y, Nishimura H, Irei I, Sadahira Y: Sphingosine-1-phosphate receptor 1 is a useful adjunct for distinguishing vascular neoplasms from morphological mimics. Virchows Arch; 2009 Feb;454(2):217-22
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • S1P(1) expression was observed in eight of eight hemangiomas, four of four lymphangiomas, four of four epithelioid hemangioendotheliomas, three of three Kaposi's sarcomas, and 15 of 15 angiosarcomas with vasoformative, spindle, epithelioid, and undifferentiated features.
  • Conventional analysis and use of a tissue microarray of soft tissue tumors revealed three of 21 liposarcomas to have weak cytoplasmic staining and one of five squamous cell carcinomas to have membranous staining in a very limited area among 115 nonvascular tumors including histological mimics of angiosarcoma such as undifferentiated carcinoma, melanoma, and epithelioid sarcoma.
  • The sensitivity with regards to the angiosarcoma cases was equal to, or even exceeded in undifferentiated angiosarcoma, that of CD31.
  • [MeSH-minor] Adult. Aged. Female. Hemangioma / diagnosis. Hemangiosarcoma / diagnosis. Humans. Immunohistochemistry. Lymphangioma / diagnosis. Male. Middle Aged

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  • (PMID = 19005676.001).
  • [ISSN] 1432-2307
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Receptors, Lysosphingolipid
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55. Tataria M, Dicker RA, Melcher M, Spain DA, Brundage SI: Spontaneous splenic rupture: the masquerade of minor trauma. J Trauma; 2005 Nov;59(5):1228-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Hemangiosarcoma / complications. Splenic Neoplasms / complications. Splenic Rupture / etiology
  • [MeSH-minor] Adult. Fatal Outcome. Female. Hemorrhage / etiology. Humans. Rupture, Spontaneous. Splenic Diseases / etiology

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  • (PMID = 16385305.001).
  • [ISSN] 0022-5282
  • [Journal-full-title] The Journal of trauma
  • [ISO-abbreviation] J Trauma
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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56. Schwab J, Haack G, Wünsch PH, Bär I, Zahn R: Cardiac angiosarcoma: case report and review of the literatur : R. R. Brandt, R. Arnold, R.M. Bohle, T. Dill, C.W. Hamm; Z Kardiol 94:824-828 (2005). Clin Res Cardiol; 2006 Jun;95(6):351-2; author reply 352-3
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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: case report and review of the literatur : R. R. Brandt, R. Arnold, R.M. Bohle, T. Dill, C.W. Hamm; Z Kardiol 94:824-828 (2005).
  • [MeSH-major] Heart Neoplasms / pathology. Hemangiosarcoma / pathology. Magnetic Resonance Imaging
  • [MeSH-minor] Adult. Humans. Male

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  • [CommentOn] Z Kardiol. 2005 Dec;94(12):824-8 [16382384.001]
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  • (PMID = 16741594.001).
  • [ISSN] 1861-0684
  • [Journal-full-title] Clinical research in cardiology : official journal of the German Cardiac Society
  • [ISO-abbreviation] Clin Res Cardiol
  • [Language] eng
  • [Publication-type] Case Reports; Comment; Letter
  • [Publication-country] Germany
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57. Burns CJ, Jammer BL, Bodnar CM: Mortality rates among chemical workers in the Kanawha Valley of West Virginia: 1940-1999. W V Med J; 2006 Jul-Aug;102(4):24-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • We observed no new cases of angiosarcoma of the liver, a cause of death previously reported in association with vinyl chloride production at the South Charleston location.
  • [MeSH-minor] Adult. Aged. Carcinogens, Environmental / adverse effects. Cause of Death. Cohort Studies. Employment. Female. Follow-Up Studies. Healthy Worker Effect. Hemangiosarcoma / chemically induced. Hemangiosarcoma / mortality. Humans. Liver Neoplasms / chemically induced. Liver Neoplasms / mortality. Lymphoma, Large B-Cell, Diffuse / chemically induced. Lymphoma, Large B-Cell, Diffuse / mortality. Lymphoma, Non-Hodgkin / chemically induced. Lymphoma, Non-Hodgkin / mortality. Male. Middle Aged. Risk. Risk Factors. Sex Factors. Time Factors. Vinyl Chloride / adverse effects. West Virginia

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  • [CommentIn] W V Med J. 2006 Sep-Oct;102(5):5 [17285946.001]
  • (PMID = 17111678.001).
  • [ISSN] 0043-3284
  • [Journal-full-title] The West Virginia medical journal
  • [ISO-abbreviation] W V Med J
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Carcinogens, Environmental; WD06X94M2D / Vinyl Chloride
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58. Barahona-Garrido J, López-Arce G, Criales S: Lower gastrointestinal bleeding in a patient with a history of breast cancer. Gastroenterology; 2010 Sep;139(3):e3-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Breast Neoplasms / therapy. Gastrointestinal Hemorrhage / etiology. Hemangiosarcoma / diagnosis. Ileal Neoplasms / diagnosis. Liver Neoplasms / diagnosis. Neoplasms, Second Primary
  • [MeSH-minor] Adult. Biopsy. Fatal Outcome. Female. Humans. Immunohistochemistry. Tomography, X-Ray Computed


59. Spira D, Ernemann U, Schulze M, Horger M: [Imaging of orbital tumors]. Rofo; 2009 Oct;181(10):925-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Adult. Calcinosis / diagnosis. Child. Contrast Media / administration & dosage. Eye / pathology. Eye Neoplasms / diagnosis. Eye Neoplasms / secondary. Hemangiosarcoma / diagnosis. Humans. Image Enhancement. Lymphoma, Non-Hodgkin / diagnosis. Meningioma / diagnosis. Optic Nerve / pathology. Optic Nerve Neoplasms / diagnosis. Orbit / pathology. Orbital Diseases / diagnosis. Orbital Pseudotumor / diagnosis. Osteosarcoma / diagnosis. Osteosarcoma / secondary. Sarcoma, Myeloid / diagnosis. Sensitivity and Specificity

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  • (PMID = 19795346.001).
  • [ISSN] 1438-9010
  • [Journal-full-title] RöFo : Fortschritte auf dem Gebiete der Röntgenstrahlen und der Nuklearmedizin
  • [ISO-abbreviation] Rofo
  • [Language] ger
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Contrast Media
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60. Deyrup AT, Miettinen M, North PE, Khoury JD, Tighiouart M, Spunt SL, Parham D, Weiss SW, Shehata BM: Angiosarcomas arising in the viscera and soft tissue of children and young adults: a clinicopathologic study of 15 cases. Am J Surg Pathol; 2009 Feb;33(2):264-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcomas arising in the viscera and soft tissue of children and young adults: a clinicopathologic study of 15 cases.
  • Angiosarcomas are rare tumors that predominantly affect adult and elderly patients and pursue an aggressive clinical course with high mortality.
  • Although angiosarcomas are well described in a variety of clinical settings, they have been incompletely characterized.
  • We identified 15 high-grade angiosarcomas arising from the viscera and soft tissue of patients 21 years old and younger from institutional and consultation files.
  • Although extremely rare, angiosarcomas do affect children and young adults and this diagnosis should be considered in atypical vascular tumors occurring in the mediastinum and those with brisk mitotic activity and/or necrosis.
  • [MeSH-major] Hemangiosarcoma / pathology. Soft Tissue Neoplasms / pathology. Viscera / pathology
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Female. Humans. Immunohistochemistry. Infant. Kaplan-Meier Estimate. Male. Prognosis

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  • (PMID = 18987547.001).
  • [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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61. 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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62. Voigtländer D, Schmidt A: [Restoration of function by microsurgical reconstruction after sarcoma excision in the upper limb]. Handchir Mikrochir Plast Chir; 2006 Aug;38(4):246-54
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  • [Title] [Restoration of function by microsurgical reconstruction after sarcoma excision in the upper limb].
  • The treatment of soft tissue sarcomas includes different modalities, but the complete excision of the tumor is the most important one.
  • [MeSH-major] Arm / surgery. Microsurgery / methods. Sarcoma / surgery. Soft Tissue Neoplasms / surgery. Surgical Flaps / blood supply
  • [MeSH-minor] Adult. Aged. Amputation / methods. Carpal Bones / surgery. Fibrosarcoma / surgery. Fingers / surgery. Forearm / radiation effects. Forearm / surgery. Hand / surgery. Hemangioendothelioma / surgery. Hemangiosarcoma / surgery. Humans. Leiomyosarcoma / surgery. Male. Middle Aged. Neoplasm Recurrence, Local / surgery. Neoplasms, Multiple Primary / surgery. Nose Neoplasms / surgery. Postoperative Complications / surgery. Radiation Injuries / surgery. Reoperation

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  • (PMID = 16991045.001).
  • [ISSN] 0722-1819
  • [Journal-full-title] Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft für Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft für Mikrochirurgie der Peripheren Nerven und Gefässe : Organ der Vereinigung der Deutschen Plastischen Chirurgen
  • [ISO-abbreviation] Handchir Mikrochir Plast Chir
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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63. Tucci E, Della Rocca C, Santilli F: Localized bacillary angiomatosis in the oral cavity: observations about a neoplasm with atypical behavior. Description of a case and review of the literature. Minerva Stomatol; 2006 Jan-Feb;55(1-2):67-75
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  • Bacillary angiomatosis can be clinically similar to the Kaposi's sarcoma and histologically confused with angiosarcoma, epitheloid hemangioma and pyogenic granuloma.
  • The high tendency to relapse, the capability in migration and to involve several localizations at the same time have induced the authors to deepen the research to exclude the possibility that it could be a Kaposi's sarcoma or a pyogenic granuloma and to get to an accurate diagnosis in order to resolve the disease.
  • [MeSH-minor] Adolescent. Adult. Ampicillin / analogs & derivatives. Ampicillin / therapeutic use. Bartonella henselae / pathogenicity. Bartonella quintana / pathogenicity. Child. Chlorhexidine / therapeutic use. Combined Modality Therapy. Diagnosis, Differential. Female. Gingival Neoplasms / diagnosis. Granuloma, Pyogenic / diagnosis. Hemangioendothelioma, Epithelioid / diagnosis. Hemangiosarcoma / diagnosis. Humans. Male. Pregnancy. Pregnancy Complications, Neoplastic / diagnosis. Recurrence. Sarcoma, Kaposi / diagnosis. Tooth Extraction

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  • (PMID = 16495874.001).
  • [ISSN] 0026-4970
  • [Journal-full-title] Minerva stomatologica
  • [ISO-abbreviation] Minerva Stomatol
  • [Language] eng; ita
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
  • [Chemical-registry-number] 7C782967RD / Ampicillin; 8GM2J22278 / bacampicillin; R4KO0DY52L / Chlorhexidine
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64. 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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  • [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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65. 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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66. 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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  • [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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67. Toro JR, Travis LB, Wu HJ, Zhu K, Fletcher CD, Devesa SS: Incidence patterns of soft tissue sarcomas, regardless of primary site, in the surveillance, epidemiology and end results program, 1978-2001: An analysis of 26,758 cases. Int J Cancer; 2006 Dec 15;119(12):2922-30
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  • [Title] Incidence patterns of soft tissue sarcomas, regardless of primary site, in the surveillance, epidemiology and end results program, 1978-2001: An analysis of 26,758 cases.
  • Soft tissue sarcomas (STS) are a heterogeneous group of uncommon tumors that show a broad range of differentiation that may reflect etiologic distinction.
  • Further, the lack of inclusion of sarcomas arising in all organs in most standard evaluations underestimates the true rates.
  • Leiomyosarcomas accounted for 23.9%, malignant fibrous histiocytomas 17.1%, liposarcomas 11.5%, dermatofibrosarcomas 10.5%, rhabdomyosarcomas 4.6% and angiosarcomas 4.1%.
  • Almost half (47.9%) of the sarcomas arose in the soft tissues, 14.0% in the skin and 7.0% in the uterus.
  • [MeSH-major] Population Surveillance / methods. Sarcoma / epidemiology
  • [MeSH-minor] Adolescent. Adult. African Americans / statistics & numerical data. Age Factors. Aged. Aged, 80 and over. Dermatofibrosarcoma / epidemiology. European Continental Ancestry Group / statistics & numerical data. Female. Hemangiosarcoma / epidemiology. Histiocytoma, Benign Fibrous / epidemiology. Humans. Incidence. Liposarcoma / epidemiology. Male. Middle Aged. Rhabdomyosarcoma / epidemiology. Sex Factors. Skin Neoplasms / epidemiology. Soft Tissue Neoplasms / epidemiology. United States / epidemiology. Uterine Neoplasms / epidemiology

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  • [Copyright] Copyright 2006 Wiley-Liss, Inc.
  • (PMID = 17013893.001).
  • [ISSN] 0020-7136
  • [Journal-full-title] International journal of cancer
  • [ISO-abbreviation] Int. J. Cancer
  • [Language] eng
  • [Grant] United States / Intramural NIH HHS / /
  • [Publication-type] Journal Article; Research Support, N.I.H., Intramural
  • [Publication-country] United States
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68. 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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69. Hyde JK, Krantz MJ, Woods JE: Intracardiac mass in a man infected with human immunodeficiency virus. Arch Pathol Lab Med; 2005 Jul;129(7):943-4
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  • [MeSH-major] HIV Infections / pathology. Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Humans. Male

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  • (PMID = 15974823.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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70. 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
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  • [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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71. 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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  • [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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72. 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
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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 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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73. 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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74. Kanitakis J: Rare skin cancers. Cancer Treat Res; 2009;146:323-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Adult. Aged. Dermatofibrosarcoma / diagnosis. Dermatofibrosarcoma / etiology. Female. Hemangiosarcoma / diagnosis. Hemangiosarcoma / etiology. Histiocytoma, Malignant Fibrous / diagnosis. Histiocytoma, Malignant Fibrous / etiology. Humans. Leiomyosarcoma / diagnosis. Leiomyosarcoma / etiology. Male. Middle Aged

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  • (PMID = 19415213.001).
  • [ISSN] 0927-3042
  • [Journal-full-title] Cancer treatment and research
  • [ISO-abbreviation] Cancer Treat. Res.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 30
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75. Matsumoto M, Tamura M, Komiya T, Aridome G, Narita R, Hisaoka M, Ohtsuki M, Otsuji Y: Hepatic angiosarcoma: a rare liver tumor in a hemodialysis patient. Clin Nephrol; 2009 May;71(5):590-2
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  • [Title] Hepatic angiosarcoma: a rare liver tumor in a hemodialysis patient.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Kidney Failure, Chronic / therapy. Liver Neoplasms / diagnosis. Renal Dialysis / methods
  • [MeSH-minor] Adult. Biopsy, Needle. Diagnosis, Differential. Fatal Outcome. Humans. Liver / pathology. Liver / radiography. Male. Tomography, X-Ray Computed

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  • (PMID = 19473625.001).
  • [ISSN] 0301-0430
  • [Journal-full-title] Clinical nephrology
  • [ISO-abbreviation] Clin. Nephrol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Germany
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76. Lang EK, Rudman E, Colon I, Macchia RJ: Hematuria: the presenting symptom of an angiosarcoma of the inferior vena cava. J Urol; 2009 Nov;182(5):2470
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  • [Title] Hematuria: the presenting symptom of an angiosarcoma of the inferior vena cava.
  • [MeSH-major] Hemangiosarcoma / complications. Hemangiosarcoma / diagnosis. Hematuria / etiology. Neoplasms, Multiple Primary / complications. Neoplasms, Multiple Primary / diagnosis. Vascular Neoplasms / complications. Vascular Neoplasms / diagnosis. Vena Cava, Inferior
  • [MeSH-minor] Adult. Humans. Male

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  • (PMID = 19765748.001).
  • [ISSN] 1527-3792
  • [Journal-full-title] The Journal of urology
  • [ISO-abbreviation] J. Urol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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77. 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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78. Tissier S, Codreanu A, Nicolas M, Laurent V, Aliot E, Regent D: [What is your diagnosis?]. J Radiol; 2005 Mar;86(3):345-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Heart Neoplasms / radiography. Hemangiosarcoma / radiography
  • [MeSH-minor] Adult. Female. Heart Atria. Humans

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  • (PMID = 15908877.001).
  • [ISSN] 0221-0363
  • [Journal-full-title] Journal de radiologie
  • [ISO-abbreviation] J Radiol
  • [Language] fre
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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79. Hsieh VW, Leung D: A rare cause of pericardial constriction in a young man. J Am Soc Echocardiogr; 2007 Feb;20(2):197.e5-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Heart Neoplasms / complications. Heart Neoplasms / ultrasonography. Hemangiosarcoma / complications. Hemangiosarcoma / ultrasonography. Pericarditis, Constrictive / etiology. Pericarditis, Constrictive / ultrasonography. Pericardium / ultrasonography
  • [MeSH-minor] Adult. Humans. Male. Rare Diseases / complications. Rare Diseases / ultrasonography

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  • (PMID = 17275708.001).
  • [ISSN] 1097-6795
  • [Journal-full-title] Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography
  • [ISO-abbreviation] J Am Soc Echocardiogr
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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80. Styring E, Fernebro J, Jönsson PE, Ehinger A, Engellau J, Rissler P, Rydholm A, Nilbert M, Vult von Steyern F: Changing clinical presentation of angiosarcomas after breast cancer: from late tumors in edematous arms to earlier tumors on the thoracic wall. Breast Cancer Res Treat; 2010 Aug;122(3):883-7
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  • [Title] Changing clinical presentation of angiosarcomas after breast cancer: from late tumors in edematous arms to earlier tumors on the thoracic wall.
  • Angiosarcoma is a rare complication of breast cancer treatment.
  • In order to define predictors, clinical presentation, and outcome, we characterized a population-based 50-year cohort of angiosarcomas after breast cancer.
  • Clinical data were collected from all females with previous breast cancer who developed angiosarcomas/lymphangiosarcomas on the thoracic wall/upper extremity between 1958 and 2008 in the Southern Swedish health care region.
  • In total, 31 angiosarcomas developed at a median age of 71 years.
  • The patients formed two distinct groups; 14 females treated for breast cancer with radical mastectomy and radiotherapy 1949-1988 developed angiosarcomas in edematous arms (Stewart-Treves syndrome) after median 11 years, and 17 females treated by segmental resection, anti-hormonal treatment and radiotherapy 1980-2005 developed angiosarcomas in the irradiated field on the thoracic wall after median 7.3 years.
  • In this population-based cohort, the early angiosarcomas developed in edematous arms after radical mastectomies, whereas more recent cases occurred after a shorter time period in the irradiated fields following breast conserving surgery.
  • We conclude that the clinical presentation of angiosarcomas has changed, parallel with altered treatment principles for breast cancer.
  • [MeSH-major] Arm. Breast Neoplasms / therapy. Edema / etiology. Hemangiosarcoma / etiology. Neoplasm Recurrence, Local / etiology. Neoplasms, Second Primary / etiology. Thoracic Wall / pathology
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Cohort Studies. Female. Humans. Middle Aged. Prognosis

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  • (PMID = 20087653.001).
  • [ISSN] 1573-7217
  • [Journal-full-title] Breast cancer research and treatment
  • [ISO-abbreviation] Breast Cancer Res. Treat.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Netherlands
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81. Soares AB, Altemani A, Furuse C, Demasi AP, Gati C, Nunes N, de Araújo VC: Intravascular papillary endothelial hyperplasia: report of 2 cases and immunohistochemical study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Nov;106(5):708-11
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  • The main significance of the lesion lies in the fact that it may be mistaken for angiosarcoma.
  • [MeSH-minor] Actins / analysis. Adult. Aged. Antigens, CD34 / analysis. Diagnosis, Differential. Female. Fibrillar Collagens / analysis. Hemangiosarcoma / diagnosis. Humans. Hyperplasia / pathology. Immunohistochemistry. Laminin / analysis. Lip Diseases / pathology. Mouth Mucosa / pathology. Mouth Neoplasms / diagnosis. Vimentin / analysis

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  • (PMID = 18929993.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Actins; 0 / Antigens, CD34; 0 / Fibrillar Collagens; 0 / Laminin; 0 / Vimentin
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82. 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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  • [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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83. 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
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  • [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


84. Contreras AL, Punar M, Tamboli P, Tu SM, Pisters L, Moran C, Czerniak BA, Guo CC: Mediastinal germ cell tumors with an angiosarcomatous component: a report of 12 cases. Hum Pathol; 2010 Jun;41(6):832-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Hemangiosarcoma / pathology. Mediastinal Neoplasms / pathology. Neoplasms, Germ Cell and Embryonal / pathology
  • [MeSH-minor] Adult. Carcinoma / mortality. Carcinoma / pathology. Humans. Leiomyosarcoma / mortality. Leiomyosarcoma / pathology. Male. Neoplasm Metastasis. Neoplasm Recurrence, Local. Rhabdomyosarcoma / mortality. Rhabdomyosarcoma / pathology. Survival Rate. Young Adult

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  • [Copyright] Copyright 2010 Elsevier Inc. All rights reserved.
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  • (PMID = 20153508.001).
  • [ISSN] 1532-8392
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / P50 CA091846
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ NIHMS614200; NLM/ PMC4163004
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85. 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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86. Zhou ML, Yan FH, Ye F, Xiong Z, Wang JH, Ji Y: [Images of primary hepatic angiosarcomas]. Zhonghua Gan Zang Bing Za Zhi; 2008 Feb;16(2):136-7
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  • [Title] [Images of primary hepatic angiosarcomas].
  • [MeSH-major] Hemangiosarcoma / radiography. Liver Neoplasms / radiography. Tomography, X-Ray Computed
  • [MeSH-minor] Adult. Aged. Female. Humans. Male. Middle Aged

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  • (PMID = 18304433.001).
  • [ISSN] 1007-3418
  • [Journal-full-title] Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology
  • [ISO-abbreviation] Zhonghua Gan Zang Bing Za Zhi
  • [Language] chi
  • [Publication-type] Journal Article
  • [Publication-country] China
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87. Deyrup AT, McKenney JK, Tighiouart M, Folpe AL, Weiss SW: Sporadic cutaneous angiosarcomas: a proposal for risk stratification based on 69 cases. Am J Surg Pathol; 2008 Jan;32(1):72-7
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  • [Title] Sporadic cutaneous angiosarcomas: a proposal for risk stratification based on 69 cases.
  • Angiosarcomas have traditionally been considered high-grade lesions for which histologic features and grading have played no role in prognostication and, consequently, they have been excluded from the American Joint Committee on Cancer staging system.
  • We have, therefore, analyzed 69 cutaneous angiosarcomas seen in consultation and not associated with lymphedema or prior radiation therapy to determine if a combination of histologic and clinical parameters could be used to differentiate indolent from aggressive tumors.
  • In conclusion, we report that a combination of clinical and histologic features allows stratification of angiosarcoma patients into 2 risk groups that are strongly associated with marked differences in clinical course.
  • [MeSH-major] Hemangiosarcoma / pathology. Skin Neoplasms / pathology
  • [MeSH-minor] Adult. Age Factors. Aged. Aged, 80 and over. Female. Humans. Male. Middle Aged. Risk Factors. Survival Analysis

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  • (PMID = 18162773.001).
  • [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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88. Tavora F, Montgomery E, Epstein JI: A series of vascular tumors and tumorlike lesions of the bladder. Am J Surg Pathol; 2008 Aug;32(8):1213-9
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  • We identified 13 lesions that included 3 hemangiomas, 3 intravascular papillary endothelial hyperplasias (Masson vegetant hemangioendotheliomas), 2 arteriovenous malformations (AVMs), 1 epithelioid hemangioendothelioma (EHE), and 4 angiosarcomas.
  • One of the angiosarcomas was associated with conventional high-grade urothelial carcinoma (sarcomatoid carcinoma).
  • There was no statistical difference among the various lesions in terms of age, although angiosarcomas tended to arise in older patients (mean 71 y vs. 60 y of the remainder).
  • All cases of angiosarcoma and EHE involved the muscularis propria.
  • Two of four patients with angiosarcoma had a history of prior radiation therapy and all 4 were dead of disease at 6 months.
  • Angiosarcomas measured 3, 4.5, 5, and 5.8 cm in greatest diameter at cystoscopy.
  • Papillary endothelial hyperplasia occurs in the bladder and must be differentiated from angiosarcoma, which has a rapidly fatal outcome.
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Arteriovenous Malformations / pathology. Endothelium, Vascular / pathology. Female. Hemangioendothelioma / pathology. Hemangioendothelioma, Epithelioid / pathology. Hemangioma / pathology. Hemangiosarcoma / pathology. Hematuria / etiology. Humans. Hyperplasia. Male. Middle Aged. Neoplasm Invasiveness. Prognosis. Retrospective Studies

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  • (PMID = 18580491.001).
  • [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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89. 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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  • [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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90. 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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91. Aghel A, Krasuski RA: A 37-year-old man with chest pain, ECG changes, and elevated cardiac enzymes. Cleve Clin J Med; 2009 Mar;76(3):199-205
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Chest Pain / etiology. Electrocardiography / methods. Heart Neoplasms / complications. Hemangiosarcoma / complications. Troponin / blood
  • [MeSH-minor] Adult. Diagnosis, Differential. Echocardiography. Heart Atria. Humans. Magnetic Resonance Imaging / methods. Male. Tomography, Emission-Computed, Single-Photon. Tomography, X-Ray Computed

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  • (PMID = 19258467.001).
  • [ISSN] 1939-2869
  • [Journal-full-title] Cleveland Clinic journal of medicine
  • [ISO-abbreviation] Cleve Clin J Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Troponin
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92. Bioulac-Sage P, Laumonier H, Laurent C, Blanc JF, Balabaud C: Benign and malignant vascular tumors of the liver in adults. Semin Liver Dis; 2008 Aug;28(3):302-14
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  • Vascular tumors of the liver in adult patients include cavernous hemangioma, a common benign tumor; epithelioid hemangioendothelioma, a rare, usually low-grade malignant tumor; and angiosarcoma, a rare and very aggressive tumor.
  • A definitive diagnosis of epithelioid hemangioendothelioma and angiosarcoma requires histopathologic examination.
  • The prognosis of angiosarcoma remains dismal.
  • [MeSH-minor] Adult. Hemangioendothelioma, Epithelioid / pathology. Hemangioendothelioma, Epithelioid / therapy. Hemangioma, Cavernous / pathology. Hemangioma, Cavernous / therapy. Hemangiosarcoma / pathology. Hemangiosarcoma / therapy. Hepatic Stellate Cells / pathology. Humans. Sarcoma, Kaposi / pathology. Sarcoma, Kaposi / therapy. Treatment Outcome

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  • (PMID = 18814083.001).
  • [ISSN] 0272-8087
  • [Journal-full-title] Seminars in liver disease
  • [ISO-abbreviation] Semin. Liver Dis.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 45
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93. 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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  • [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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94. 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
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  • [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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95. 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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96. Bansal M, Mehrotra R, Agrawal V, Kasliwal RR, Trehan N: Primary tumor of the heart. Angiosarcoma. Indian Heart J; 2009 Jul-Aug;61(4):383
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary tumor of the heart. Angiosarcoma.
  • [MeSH-major] Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Humans. Lymphoma / diagnosis. Male

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  • (PMID = 20635745.001).
  • [ISSN] 0019-4832
  • [Journal-full-title] Indian heart journal
  • [ISO-abbreviation] Indian Heart J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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97. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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98. Goldberg J, Losman JA, Cavanaugh K: A bleeding heart. Am J Med; 2006 Dec;119(12):1029-32
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis
  • [MeSH-minor] Adult. Female. Heart Diseases / etiology. Hemorrhage / etiology. Humans

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  • (PMID = 17145243.001).
  • [ISSN] 1555-7162
  • [Journal-full-title] The American journal of medicine
  • [ISO-abbreviation] Am. J. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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99. Burjonroppa SC, Reardon MJ, Swafford J: Images in cardiology: Right atrial mass: primary angiosarcoma. Heart; 2005 Oct;91(10):1271
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Images in cardiology: Right atrial mass: primary angiosarcoma.
  • [MeSH-major] Heart Neoplasms / ultrasonography. Hemangiosarcoma / ultrasonography
  • [MeSH-minor] Adult. Echocardiography, Transesophageal. Heart Atria. Humans. Male

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  • (PMID = 16162612.001).
  • [ISSN] 1468-201X
  • [Journal-full-title] Heart (British Cardiac Society)
  • [ISO-abbreviation] Heart
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC1769126
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100. Kairi-Vassilatou E, Grapsa D, Kontogianni-Katsarou K, Smyrniotis V, Hasiakos D, Agatha AK: Clinicopathological features of unusual vascular lesions of the pelvis, retroperitoneum and colon in females: a report of five cases and review of the literature. Eur J Gynaecol Oncol; 2006;27(3):250-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • In our study we describe five diverse and unusual cases of vascular lesions of the pelvis, retroperitoneum and colon in female patients: a case of retroperitoneal angiosarcoma, pelvic hemangioendothelioma, pelvic angiomyxoma, retroperitoneal lymphangioleiomyomatosis and a case of diffuse cavernous hemangiomatosis of the colon, with emphasis on their clinicopathological features and differential diagnosis.
  • [MeSH-minor] Adult. Female. Hemangioendothelioma / pathology. Hemangioma, Cavernous / pathology. Hemangiosarcoma / pathology. Humans. Lymphangioleiomyomatosis / pathology. Middle Aged. Myxoma / pathology

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  • (PMID = 16800252.001).
  • [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] 35
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