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Items 1 to 96 of about 96
1. Oztürk E, Mutlu H, Sönmez G, Sildiroğlu HO: Primary angiosarcoma of the spleen. Turk J Gastroenterol; 2007 Dec;18(4):272-5
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  • [Title] Primary angiosarcoma of the spleen.
  • Primary angiosarcoma of the spleen is a rare neoplasm with a very poor prognosis.
  • We present computed tomography and magnetic resonance imaging of a 49-year-old man with primary splenic angiosarcoma and liver metastasis.
  • The literature on primary splenic angiosarcoma is reviewed and imaging variability of this rare tumor is discussed.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Splenic Neoplasms / diagnosis

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  • (PMID = 18080928.001).
  • [ISSN] 2148-5607
  • [Journal-full-title] The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology
  • [ISO-abbreviation] Turk J Gastroenterol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Turkey
  • [Number-of-references] 23
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2. Aviles-Salas A, Luévano-González A: [Primary angiosarcoma of the spleen: report of one case]. Rev Med Chil; 2007 Sep;135(9):1178-81

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  • [Title] [Primary angiosarcoma of the spleen: report of one case].
  • [Transliterated title] Angiosarcoma primario del bazo: Caso clínico.
  • Primary angiosarcoma of the spleen is rare and almost always fatal.
  • It has an aggressive behavior and frequently presents with hematological abnormalities or metastatic disease.
  • He was subjected to a splenectomy and the biopsy disclosed an angiosarcoma of the spleen.
  • [MeSH-major] Hemangiosarcoma / pathology. Splenic Neoplasms / pathology

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  • (PMID = 18064374.001).
  • [ISSN] 0034-9887
  • [Journal-full-title] Revista médica de Chile
  • [ISO-abbreviation] Rev Med Chil
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Chile
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3. Rohan VS, Hanji AM, Patel JJ, Tankshali RA: Primary angiosarcoma of the breast in a postmenopausal patient. J Cancer Res Ther; 2010 Jan-Mar;6(1):120-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the breast in a postmenopausal patient.
  • Primary angiosarcoma of the breast is a rare entity forming 0.04% of primary breast tumors.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology

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  • (PMID = 20479566.001).
  • [ISSN] 1998-4138
  • [Journal-full-title] Journal of cancer research and therapeutics
  • [ISO-abbreviation] J Cancer Res Ther
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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4. Pandit SA, Fiedler PN, Westcott JL: Primary angiosarcoma of the lung. Ann Diagn Pathol; 2005 Oct;9(5):302-4
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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 lung.
  • Primary angiosarcoma of the lung is a rare disorder with few cases reported in the literature [Patel AM, Ryu JH.
  • Angiosarcoma in the lung.
  • We present a case of primary angiosarcoma of the lung in a 79-year-old woman.
  • The histologic, cytologic, and immunophenotypic features were characteristic of epithelioid angiosarcoma.
  • [MeSH-major] Hemangiosarcoma / pathology. Lung Neoplasms / pathology

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  • (PMID = 16198962.001).
  • [ISSN] 1092-9134
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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5. Böge G, Gallix B, Gresillon C, Khau Van Kien A, Veerapen R, Quéré I: [Primary angiosarcoma of the aorta]. Vasa; 2007 Feb;36(1):33-40
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  • [Title] [Primary angiosarcoma of the aorta].
  • [Transliterated title] Primäres Angiosarkom der Aorta.
  • Primary angiosarcoma of the aorta is a rare disease.
  • The prognosis is poor, resulting of embolic complications and early metastatic disease, with a median survival of nine months.
  • We report the case of a 68-year-old woman referred for a thrombosis of the superior mesenteric artery, occurring a few weeks after resection of an angiosarcoma of the small intestine, disclosing a primary angiosarcoma of the aortic wall with metastatic disease.
  • [MeSH-major] Aorta, Thoracic. Aortic Diseases / diagnosis. Hemangiosarcoma / diagnosis. Mesenteric Artery, Superior. Mesenteric Vascular Occlusion / etiology. Thrombosis / etiology. Vascular Neoplasms / diagnosis

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  • (PMID = 17323296.001).
  • [ISSN] 0301-1526
  • [Journal-full-title] VASA. Zeitschrift für Gefässkrankheiten
  • [ISO-abbreviation] VASA
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Switzerland
  • [Number-of-references] 34
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6. Bhati CS, Bhatt AN, Starkey G, Hubscher SG, Bramhall SR: Acute liver failure due to primary angiosarcoma: a case report and review of literature. World J Surg Oncol; 2008 Sep 30;6:104
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  • [Title] Acute liver failure due to primary angiosarcoma: a case report and review of literature.
  • BACKGROUND: Hepatic angiosarcoma is a primary sarcoma of the liver, accounting for only 2% of all primary hepatic malignancies.
  • Acute liver failure is an extremely rare presentation of a primary liver tumour.
  • On further investigation he was found to have primary angiosarcoma of liver.
  • CONCLUSION: The treatment outcomes for hepatic angiosarcoma are poor, we discuss the options available and the need for prompt investigation and establishment of a diagnosis.
  • [MeSH-major] Hemangiosarcoma / complications. Liver Failure, Acute / etiology. Liver Neoplasms / complications

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  • [Cites] Hepatogastroenterology. 2007 Mar;54(74):533-5 [17523315.001]
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  • (PMID = 18826593.001).
  • [ISSN] 1477-7819
  • [Journal-full-title] World journal of surgical oncology
  • [ISO-abbreviation] World J Surg Oncol
  • [Language] eng
  • [Grant] United Kingdom / Medical Research Council / / G0701304
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 28
  • [Other-IDs] NLM/ PMC2567320
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7. Hidaka Y, Hagio M, Uchida K, Hara Y: Primary hemangiosarcoma of the humerus in a Maltese dog. J Vet Med Sci; 2006 Aug;68(8):895-8
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  • [Title] Primary hemangiosarcoma of the humerus in a Maltese dog.
  • Histopathologically, the dog was diagnosed with primary hemangiosarcoma of the humerus.
  • Thereafter, metastatic lesions appeared in the skin, and the dog was euthanized 1 month after the operation.

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  • (PMID = 16953096.001).
  • [ISSN] 0916-7250
  • [Journal-full-title] The Journal of veterinary medical science
  • [ISO-abbreviation] J. Vet. Med. Sci.
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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8. Ryu DY, Hwang SY, Lee DW, Kim TO, Park DY, Kim GH, Heo J, Kang DH, Song GA, Cho M: [A case of primary angiosarcoma of small intestine presenting as recurrent gastrointestinal bleeding]. Korean J Gastroenterol; 2005 Nov;46(5):404-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [A case of primary angiosarcoma of small intestine presenting as recurrent gastrointestinal bleeding].
  • Angiosarcoma is a rare malignant tumor which occurs frequently in the skin and soft subcutis.
  • Moreover, primary gastrointestinal angiosarcomas are very rare.
  • This tumor manifests as non-specific symptoms such as gastrointestinal bleeding, abdominal pain and nausea.
  • We report a case of primary angiosarcoma of the small intestine presenting as recurrent gastrointestinal bleeding.
  • The ileal mass was diagnosed as angiosarcoma on immunohistochemical stain.
  • [MeSH-major] Gastrointestinal Hemorrhage / etiology. Hemangiosarcoma / diagnosis. Intestinal Neoplasms / diagnosis. Intestine, Small

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  • (PMID = 16301855.001).
  • [ISSN] 1598-9992
  • [Journal-full-title] The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi
  • [ISO-abbreviation] Korean J Gastroenterol
  • [Language] kor
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Korea (South)
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9. Kim JB, Kim SH, Lim SY, Roh SY, Cho GY, Song HJ, Park S, Lee J, Kim SJ: Primary angiosarcoma of the pulmonary trunk mimicking pulmonary thromboembolism. Echocardiography; 2010 Feb;27(2):E23-6

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

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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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10. Liu H, Zhao J, Fan Y, Fu XL, Fu L: [Clinical and pathologic characteristics of primary angiosarcoma of breast]. Zhonghua Bing Li Xue Za Zhi; 2006 Oct;35(10):598-601
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Clinical and pathologic characteristics of primary angiosarcoma of breast].
  • OBJECTIVE: To study the clinical and pathologic characteristics of primary angiosarcoma of breast.
  • METHODS: Five cases of primary angiosarcoma of breast were reviewed.
  • CONCLUSIONS: Primary angiosarcoma of breast is a rare entity.
  • [MeSH-major] Breast Neoplasms / pathology. Breast Neoplasms, Male / pathology. Hemangiosarcoma / pathology

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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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11. Losanoff JE, Jaber S, Esuba M, Perry M, Sauter ER: Primary angiosarcoma of the breast: do enlarged axillary nodes matter? Breast J; 2006 Jul-Aug;12(4):371-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the breast: do enlarged axillary nodes matter?
  • Primary angiosarcoma of the breast is a rare and aggressive malignancy that is typically seen in premenopausal patients.
  • We present a case of breast angiosarcoma presenting with enlarged axillary lymph nodes treated with a modified mastectomy and axillary lymph node dissection.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology. Lymph Nodes / pathology

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  • (PMID = 16848851.001).
  • [ISSN] 1075-122X
  • [Journal-full-title] The breast journal
  • [ISO-abbreviation] Breast J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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12. Forton GE, Van Parys G, Hertveldt K: Primary angiosarcoma of the non-irradiated parotid gland: a most uncommon, highly malignant tumor. Eur Arch Otorhinolaryngol; 2005 Mar;262(3):173-7
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  • [Title] Primary angiosarcoma of the non-irradiated parotid gland: a most uncommon, highly malignant tumor.
  • This case report discusses the clinical presentation, imaging, surgery and further treatment and course of a primary angiosarcoma of a non-irradiated parotid gland.
  • [MeSH-major] Hemangiosarcoma / secondary. Parotid Neoplasms / pathology. Skin Neoplasms / secondary
  • [MeSH-minor] Aged. Aged, 80 and over. Antigens, CD45 / immunology. Humans. Keratins / immunology. Magnetic Resonance Imaging. Male. Neoplasm Staging. Neoplasms, Second Primary / diagnostic imaging. Neoplasms, Second Primary / pathology. Tomography, X-Ray Computed

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  • (PMID = 15133686.001).
  • [ISSN] 0937-4477
  • [Journal-full-title] European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
  • [ISO-abbreviation] Eur Arch Otorhinolaryngol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 68238-35-7 / Keratins; EC 3.1.3.48 / Antigens, CD45
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13. Saglik Y, Yildiz Y, Atalar H, Basarir K: Primary angiosarcoma of the fibula : a case report. Acta Orthop Belg; 2007 Dec;73(6):799-803
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  • [Title] Primary angiosarcoma of the fibula : a case report.
  • Primary vascular neoplasms of bone are rare and have a poor prognosis.
  • Angiosarcoma of bone originates in vascular endothelial cells within bone tissue.
  • Here we present a 72-year-old male patient who had primary angiosarcoma of the fibula.
  • [MeSH-major] Bone Neoplasms / diagnosis. Fibula. Hemangiosarcoma / diagnosis

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  • (PMID = 18260498.001).
  • [ISSN] 0001-6462
  • [Journal-full-title] Acta orthopaedica Belgica
  • [ISO-abbreviation] Acta Orthop Belg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Belgium
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14. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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

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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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15. Indelicato DJ, Keole SR, Shahlaee AH, Morris CG, Gibbs CP, Scarborough MT, Islam S, Marcus RB: Ewing tumors of the chest wall: Local control and long-term outcomes. J Clin Oncol; 2009 May 20;27(15_suppl):e21501

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • : e21501 Background: Primary sarcomas of the lungs and mediastinum are rare and few data are reported on treatment and results of therapy.
  • 4 pts had a previous history of mediastinal radiation for Hodgkin's and non-Hodgkin's linfomas.
  • 26 lung sarcomas presented as a singular mass in 23 cases and as a metastatic disease in 3.
  • The histology were: peripheral nerve tumour 7, leiomyosarcoma 4, MFH 2, fibrosarcoma 2, liposarcoma 1, angiosarcoma 2, undifferentiated sarcoma 1, solitary fibrous tumour 2, rhabdomyosarcoma 2, synovialsarcoma 2, pulmonary artery sarcoma 1, pleuropolmonary blastoma 1, malignant hemangiopericytoma 1, mixoid chondrosarcoma 1, ectopic osteosarcoma 1, aggressive fibromatosis 1.
  • Local relapse or metastatic progression were recorded in 16/23 pts and 12 received one or more lines of palliative CT.
  • CONCLUSIONS: Primary sarcomas of the lungs and mediastinum have a very severe prognosis.

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  • (PMID = 27963390.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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16. Comandone A, Boglione A, Pochettino P, Berno E, Inguì M, Papotti M, Borasio P, Maggi G, Brach Del Prever E, Gino G: Primary sarcomas of the lungs and mediastinum: Clinicopathological study and therapy results of Piedmontese Group for Sarcomas. J Clin Oncol; 2009 May 20;27(15_suppl):e21509

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary sarcomas of the lungs and mediastinum: Clinicopathological study and therapy results of Piedmontese Group for Sarcomas.
  • : e21509 Background: Primary sarcomas of the lungs and mediastinum are rare and few data are reported on treatment and results of therapy.
  • 4 pts had a previous history of mediastinal radiation for Hodgkin's and non-Hodgkin's linfomas.
  • 26 lung sarcomas presented as a singular mass in 23 cases and as a metastatic disease in 3.
  • The histology were: peripheral nerve tumour 7, leiomyosarcoma 4, MFH 2, fibrosarcoma 2, liposarcoma 1, angiosarcoma 2, undifferentiated sarcoma 1, solitary fibrous tumour 2, rhabdomyosarcoma 2, synovialsarcoma 2, pulmonary artery sarcoma 1, pleuropolmonary blastoma 1, malignant hemangiopericytoma 1, mixoid chondrosarcoma 1, ectopic osteosarcoma 1, aggressive fibromatosis 1.
  • Local relapse or metastatic progression were recorded in 16/23 pts and 12 received one or more lines of palliative CT.
  • CONCLUSIONS: Primary sarcomas of the lungs and mediastinum have a very severe prognosis.

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  • (PMID = 27963441.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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17. Altan E, Arslan C, Dede D, Dogan E, Altundag K: Primary Angiosarcoma of the Breast after Pregnancy. Am Surg; 2010 Aug 01;76(8):115

  • [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.

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  • (PMID = 28958226.001).
  • [ISSN] 1555-9823
  • [Journal-full-title] The American surgeon
  • [ISO-abbreviation] Am Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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18. Koutelidakis IM, Tsiaousis PZ, Papaziogas BT, Patsas AG, Atmatzidis SK, Atmatzidis KS: Spleen rupture due to primary angiosarcoma: a case report. J Gastrointest Cancer; 2007;38(2-4):74-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Spleen rupture due to primary angiosarcoma: a case report.
  • A case of a 79-year-old female with rupture of the spleen due to primary angiosarcoma is presented.
  • Symptoms were non-specific.
  • Primary angiosarcoma of the spleen is a very rare and aggressive neoplasm with a high metastatic rate and almost uniformly fatal.
  • [MeSH-major] Hemangiosarcoma / complications. Splenic Neoplasms / complications. Splenic Rupture / etiology

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  • (PMID = 19016352.001).
  • [ISSN] 1941-6628
  • [Journal-full-title] Journal of gastrointestinal cancer
  • [ISO-abbreviation] J Gastrointest Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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19. Shet T, Malaviya A, Nadkarni M, Kakade A, Parmar V, Badwe R, Chinoy R: Primary angiosarcoma of the breast: observations in Asian Indian women. J Surg Oncol; 2006 Oct 1;94(5):368-74
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the breast: observations in Asian Indian women.
  • BACKGROUND: Primary angiosarcomas of breast are rare tumors, with a fatal outcome.
  • RESULTS: All patients had primary angiosarcoma; no case of secondary angiosarcoma was accessioned during the study period.
  • Interesting cases encountered included an epithelioid angiosarcoma and an angiosarcoma arising on the background of a biphasic tumor.
  • The patient with well-differentiated angiosarcoma also died of metastasis albeit after a longer time.
  • CONCLUSION: Primary angiosarcoma was fatal in young Indian women even in lower grade tumors.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology. Proto-Oncogene Proteins c-kit / biosynthesis

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  • [Copyright] Copyright (c) 2006 Wiley-Liss, Inc.
  • (PMID = 16967461.001).
  • [ISSN] 0022-4790
  • [Journal-full-title] Journal of surgical oncology
  • [ISO-abbreviation] J Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] EC 2.7.10.1 / Proto-Oncogene Proteins c-kit
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20. Winter L, Langrehr J, Hänninen EL: Primary angiosarcoma of the abdominal aorta: multi-row computed tomography. Abdom Imaging; 2010 Aug;35(4):485-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the abdominal aorta: multi-row computed tomography.
  • Primary angiosarcoma of the aorta is a rare tumor.
  • We report on interventional and CT-angiographic features of an abdominal aortic angiosarcoma, observed in a 71-year-old patient.
  • [MeSH-major] Aorta, Abdominal. Hemangiosarcoma / radiography. Tomography, X-Ray Computed. Vascular Neoplasms / radiography

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  • (PMID = 19462198.001).
  • [ISSN] 1432-0509
  • [Journal-full-title] Abdominal imaging
  • [ISO-abbreviation] Abdom Imaging
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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21. Lach B, Hassounah M, Khafaga Y: Primary angiosarcoma of the brain in a child. Fetal Pediatr Pathol; 2008;27(3):175-83
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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 brain in a child.
  • We describe a pediatric case of primary angiosarcoma of the brain displaying striking intravascular papillary pattern, consistent with the "Dabska tumor," often in continuity with a massive, multifocal intravascular papillary endothelial hyperplasia.
  • Colocalization of these lesions suggests the development of a papillary angiosarcoma in the pre-existing vascular malformation.
  • [MeSH-major] Brain Neoplasms. Hemangiosarcoma. Neoplasms, Vascular Tissue

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  • (PMID = 18633770.001).
  • [ISSN] 1551-3823
  • [Journal-full-title] Fetal and pediatric pathology
  • [ISO-abbreviation] Fetal Pediatr Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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22. Hsu JT, Ueng SH, Hwang TL, Chen HM, Jan YY, Chen MF: Primary angiosarcoma of the spleen in a child with long-term survival. Pediatr Surg Int; 2007 Aug;23(8):807-10

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the spleen in a child with long-term survival.
  • Primary angiosarcoma of the spleen is a very rare and aggressive neoplasm with poor prognosis.
  • Splenic angiosarcoma rarely occurs in the pediatric group (18 years or younger).
  • We report a 7-year-old boy with splenic angiosarcoma presented with left upper quadrant abdominal pain and a palpable abdominal mass.
  • Histological examination of the surgical specimen showed that this tumor had typical feature of angiosarcoma including vasoformative architecture, highly pleomorphic tumor cells with irregular, hyperchromatic and prominent nucleoli, and some mitosis.
  • This is the longest reported duration of survival in a patient with splenic angiosarcoma.
  • [MeSH-major] Hemangiosarcoma. Splenic Neoplasms

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  • [Cites] J Surg Oncol. 1996 Mar;61(3):170-6 [8637202.001]
  • [Cites] Int Surg. 1980 Jul-Aug;65(4):369-73 [7194868.001]
  • [Cites] Med Pediatr Oncol. 2003 Jun;40(6):411-2 [12692821.001]
  • [Cites] Am J Surg Pathol. 1997 Jul;21(7):827-35 [9236839.001]
  • [Cites] Pediatr Hematol Oncol. 2005 Jul-Aug;22(5):387-90 [16020128.001]
  • [Cites] Mod Pathol. 2000 Sep;13(9):978-87 [11007038.001]
  • [Cites] Pediatr Pathol. 1985;4(3-4):331-9 [3835556.001]
  • [Cites] Arch Pathol Lab Med. 1979 Mar;103(3):122-4 [581838.001]
  • [Cites] Cancer. 1996 Jun 1;77(11):2400-6 [8635113.001]
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  • (PMID = 17641924.001).
  • [ISSN] 0179-0358
  • [Journal-full-title] Pediatric surgery international
  • [ISO-abbreviation] Pediatr. Surg. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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23. 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.
  • Forty-nine cases of primary angiosarcoma of the breast were retrieved from our files.
  • Histologically, primary tumors were graded using Rosen's 3-tier system: 17 tumors (35.4%) as low grade, 17 (35.4%) as intermediate grade, and 14 (29.2%) as high grade.
  • 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.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology

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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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24. Fujii Y, Koibuchi-Yamaoka H, Taniguchi N, Yasuda Y, Nagai H: Metastasis from a primary angiosarcoma of the scalp to the colon: sonographic and CT findings. J Clin Ultrasound; 2008 Feb;36(2):110-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metastasis from a primary angiosarcoma of the scalp to the colon: sonographic and CT findings.
  • We report a case of metastasis to the colon from a primary angiosarcoma of the scalp in a 61-year-old Japanese man and describe the sonographic features and CT findings, with a brief discussion of the clinical and histopathologic findings.
  • Although this entity is extremely rare, it should be considered when a patient with prior diagnosis of angiosarcoma in another organ has focal thickening with preserved compressibility of the wall of the colon.
  • [MeSH-major] Colonic Neoplasms / secondary. Head and Neck Neoplasms / pathology. Hemangiosarcoma / secondary. Scalp. Skin Neoplasms / pathology. Tomography, X-Ray Computed / methods. Ultrasonography, Doppler / methods

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  • [Copyright] (c) 2007 Wiley Periodicals, Inc.
  • (PMID = 17636504.001).
  • [ISSN] 0091-2751
  • [Journal-full-title] Journal of clinical ultrasound : JCU
  • [ISO-abbreviation] J Clin Ultrasound
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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25. Isa NM, James DT, Saw TH, Pennisi R, Gough I: Primary angiosarcoma of the thyroid gland with recurrence diagnosed by fine needle aspiration: a case report. Diagn Cytopathol; 2009 Jun;37(6):427-32
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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 thyroid gland with recurrence diagnosed by fine needle aspiration: a case report.
  • Angiosarcoma of the thyroid is a rare and aggressive primary malignant tumor of the thyroid originally reported in patients from the Swiss Alpine region.
  • We describe a case of primary angiosarcoma of the thyroid in a 48-year-old female, who presented with a rapidly enlarging neck mass associated with compressive symptoms.
  • A diagnosis of poorly differentiated malignant tumor consistent with angiosarcoma was made.
  • Second aspiration cytology of the recurrent tumor yielded hypocellular smears containing singularly dispersed atypical cells having eccentrically-placed nuclei with prominent macronucleoli and intracytoplasmic vacuoles within a background of inflammatory cells, consistent with recurrent angiosarcoma.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Hemangiosarcoma / pathology. Thyroid Gland / pathology

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  • [Copyright] (c) 2009 Wiley-Liss, Inc.
  • (PMID = 19306411.001).
  • [ISSN] 1097-0339
  • [Journal-full-title] Diagnostic cytopathology
  • [ISO-abbreviation] Diagn. Cytopathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD31
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26. Hsu JT, Chen HM, Lin CY, Yeh CN, Hwang TL, Jan YY, Chen MF: Primary angiosarcoma of the spleen. J Surg Oncol; 2005 Dec 15;92(4):312-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the spleen.
  • BACKGROUND AND OBJECTIVES: Primary splenic angiosarcoma is a very rare and aggressive neoplasm with a high metastatic rate and dismal prognosis.
  • METHODS: The records of all cases of primary splenic angiosarcoma treated at Chang Gung Memorial Hospital from April 1991 to July 2004 were retrospectively reviewed.
  • CONCLUSIONS: The clinical presentations of splenic angiosarcoma were similar to those of previous reports apart from the higher rate of splenomegaly observed in this study.
  • [MeSH-major] Hemangiosarcoma. Splenic Neoplasms

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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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27. Seethala RR, Gomez JA, Vakar-Lopez F: Primary angiosarcoma of the bladder. Arch Pathol Lab Med; 2006 Oct;130(10):1543-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the bladder.
  • CONTEXT: Primary bladder angiosarcomas are extremely rare, and their clinical and pathologic features are not well described.
  • OBJECTIVE: To further refine the clinical features of primary bladder angiosarcomas and define their pathologic spectra.
  • STUDY SELECTION: After excluding 4 cases that likely secondarily involved the bladder, we identified 9 true primary bladder angiosarcomas.
  • DATA SYNTHESIS: Primary bladder angiosarcomas were found at a mean age of 64.2 years, with a male-female ratio of 8:1.
  • Primary bladder angiosarcomas typically presented with hematuria and were grossly hemorrhagic, raised masses (mean size, 6.7 cm) of the trigone and/or dome.
  • CONCLUSIONS: Primary angiosarcomas of the bladder are typically rare tumors of middle-aged and elderly men that present with locally advanced disease and show a wide histologic spectrum.
  • [MeSH-major] Hemangiosarcoma / complications. Hemangiosarcoma / pathology. Hematuria / etiology. Hemorrhage / etiology. Urinary Bladder / blood supply. Urinary Bladder Neoplasms / complications. Urinary Bladder Neoplasms / pathology

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  • (PMID = 17090199.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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28. Hadidy A, Alsharif A, Sheikh-Ali R, Abukhalaf M, Awidi A, Abukaraki A, Nimri C, Omari A: Odontogenic myxofibroma synchronous with primary angiosarcoma of the spleen. Br J Radiol; 2010 Jan;83(985):e10-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Odontogenic myxofibroma synchronous with primary angiosarcoma of the spleen.
  • Odontogenic myxofibroma of the temporomandibular joint (TMJ) is a rare tumour; moreover, primary splenic angiosarcoma (PAS) in paediatric patients is extremely rare.
  • The TMJ swelling proved to be odontogenic myxofibroma and the abdominal pain was a result of primary splenic angiosarcoma with hepatic metastasis.
  • [MeSH-major] Fibroma / diagnosis. Hemangiosarcoma / diagnosis. Neoplasms, Multiple Primary / diagnosis. Odontogenic Tumors / diagnosis. Splenic Neoplasms / diagnosis. Temporomandibular Joint Disorders / diagnosis

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  • [Cites] Abdom Imaging. 2000 May-Jun;25(3):283-5 [10823452.001]
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  • (PMID = 20139242.001).
  • [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/ PMC3487256
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29. Granier G, Lemoine MC, Mares P, Pignodel C, Marty-Double C: [Primary angiosarcoma of the male breast]. Ann Pathol; 2005 Jun;25(3):235-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Primary angiosarcoma of the male breast].
  • [Transliterated title] Angiosarcome primitif du sein chez l'homme.
  • We report an exceptional case of primary breast angiosarcoma in a 58-year-old man.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology

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  • (PMID = 16230950.001).
  • [ISSN] 0242-6498
  • [Journal-full-title] Annales de pathologie
  • [ISO-abbreviation] Ann Pathol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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30. Timóteo AT, Branco LM, Bravio I, Pinto E, Timoteo T, Matos P, Ferreira RC: Primary angiosarcoma of the pericardium: case report and review of the literature. Kardiol Pol; 2010 Jul;68(7):802-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the pericardium: case report and review of the literature.
  • Primary cardiac tumours are rare entities and angiosarcoma is the most frequent primary cardiac malignant tumour.
  • We present the case of a 50 year-old patient with localised pericardial angiosarcoma who survived 23 months after diagnosis with a combined approach of chemotherapy and surgery.
  • [MeSH-major] Heart Neoplasms / pathology. Heart Neoplasms / therapy. Hemangiosarcoma / pathology. Hemangiosarcoma / therapy. Pericardium / pathology

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  • (PMID = 20648441.001).
  • [ISSN] 0022-9032
  • [Journal-full-title] Kardiologia polska
  • [ISO-abbreviation] Kardiol Pol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Poland
  • [Number-of-references] 11
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31. Mendiz O, Lev G, Valdivieso L, Fava C, Gallucci E, Baldessari E, Favaloro R: Lifesaving kissing stent for pulmonary trunk stenosis due to primary angiosarcoma. Ann Vasc Surg; 2010 Nov;24(8):1135.e9-12

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Lifesaving kissing stent for pulmonary trunk stenosis due to primary angiosarcoma.
  • [MeSH-major] Arterial Occlusive Diseases / therapy. Endovascular Procedures / instrumentation. Hemangiosarcoma / complications. Pulmonary Artery. Stents. Vascular Neoplasms / complications

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  • [Copyright] Copyright © 2010 Annals of Vascular Surgery Inc. Published by Elsevier Inc. All rights reserved.
  • (PMID = 21035708.001).
  • [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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32. Nakajima H, Kobayashi J, Matsuda H, Ishibashi-Ueda H: A primary angiosarcoma in the aorta. Interact Cardiovasc Thorac Surg; 2007 Dec;6(6):832-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A primary angiosarcoma in the aorta.
  • We present herein a huge primary sarcoma in the abdominal aorta, which has been reported as extremely rare.
  • [MeSH-major] Aorta / pathology. Arterial Occlusive Diseases / complications. Hemangiosarcoma / diagnosis. Multiple Organ Failure / etiology. Vascular Neoplasms / diagnosis

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  • (PMID = 17699542.001).
  • [ISSN] 1569-9285
  • [Journal-full-title] Interactive cardiovascular and thoracic surgery
  • [ISO-abbreviation] Interact Cardiovasc Thorac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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33. Armah HB, Rao UN, Parwani AV: Primary angiosarcoma of the testis: report of a rare entity and review of the literature. Diagn Pathol; 2007;2:23
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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 testis: report of a rare entity and review of the literature.
  • BACKGROUND: Primary testicular angiosarcomas are extremely rare, and their clinicopathologic features are not well described.
  • Our objective was to further define the clinical features and pathologic spectra of primary testicular angiosarcomas.
  • After excluding 2 cases because they did not involve the testis, we identified 4 previously reported cases of true primary testicular angiosarcoma.
  • We also searched the electronic medical archival records of our institution and identified one additional unreported case of true primary testicular angiosarcomas.
  • Data were extracted on the demographics, predisposing factors, clinical presentation, gross pathology, microscopic pathology, immunophenotype, therapy, and outcomes of each of these 5 cases of true primary testicular angiosarcomas.
  • RESULTS: Primary testicular angiosarcomas were found at a mean age of 43.4 years.
  • One patient had multiple metastatic recurrences but eventual outcome was not available, and 1 patient died a month after diagnosis from stroke but no autopsy was performed.
  • CONCLUSION: Primary testicular angiosarcomas are typically rare tumors of men of all ages that appear to segregate into 2 groups; one associated with teratoma and occurring in young people, and the other occurring in the elderly and not associated with germ cell neoplasm, but may be associated with chronic hydrocele.

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  • (PMID = 17601346.001).
  • [ISSN] 1746-1596
  • [Journal-full-title] Diagnostic pathology
  • [ISO-abbreviation] Diagn Pathol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC1919353
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34. Brylka D, Demos TC, Pierce K: Primary angiosarcoma of the abdominal aorta: a case report and literature review (aortic angiosarcoma). Abdom Imaging; 2009 Mar-Apr;34(2):239-42
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the abdominal aorta: a case report and literature review (aortic angiosarcoma).
  • Fewer than 140 cases of aortic sarcoma have been reported with only 34 classified as angiosarcoma.
  • Angiosarcoma was an unexpected pathologic diagnosis based on tissue removed during aortobifemoral bypass surgery.
  • [MeSH-major] Aorta, Abdominal. Hemangiosarcoma / radiography. Vascular Neoplasms / radiography

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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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35. Verge J, Albiol J, Navas M, Martín C: [Primary angiosarcoma of the spleen with liver metastases. Case report and literature review]. Cir Esp; 2005 Jul;78(1):50-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Primary angiosarcoma of the spleen with liver metastases. Case report and literature review].
  • [Transliterated title] Angiosarcoma primario de bazo con metástasis hepáticas: presentación de un caso y revisión de la bibliografía.
  • [MeSH-major] Hemangiosarcoma / secondary. Hemangiosarcoma / surgery. Liver Neoplasms / secondary. Liver Neoplasms / surgery. Splenic Neoplasms / pathology. Splenic Neoplasms / surgery

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  • (PMID = 16420791.001).
  • [ISSN] 0009-739X
  • [Journal-full-title] Cirugía española
  • [ISO-abbreviation] Cir Esp
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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36. Bradford L, Swartz K, Rose S: Primary angiosarcoma of the ovary complicated by hemoperitoneum: a case report and review of the literature. Arch Gynecol Obstet; 2010 Jan;281(1):145-50
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the ovary complicated by hemoperitoneum: a case report and review of the literature.
  • A small subset of these, primary ovarian angiosarcoma, is even more rare, with only 26 cases reported in the literature.
  • She underwent a full staging and optimal debulking that revealed Stage IIIC primary ovarian angiosarcoma.
  • The patient died 3 weeks post-operatively secondary to hemorrhage from progressive, metastatic tumor sites prior to initiation of chemotherapy.
  • CONCLUSION: Primary ovarian angiosarcoma is extremely rare, often presenting in later stages with nonspecific symptoms.
  • [MeSH-major] Hemangiosarcoma / complications. Hemoperitoneum / etiology. Ovarian Neoplasms / complications

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  • (PMID = 19396453.001).
  • [ISSN] 1432-0711
  • [Journal-full-title] Archives of gynecology and obstetrics
  • [ISO-abbreviation] Arch. Gynecol. Obstet.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Germany
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37. Akkad T, Tsankov A, Pelzer A, Peschel R, Bartsch G, Steiner H: Early diagnosis and straight forward surgery of an asymptomatic primary angiosarcoma of the kidney led to long-term survival. Int J Urol; 2006 Aug;13(8):1112-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Early diagnosis and straight forward surgery of an asymptomatic primary angiosarcoma of the kidney led to long-term survival.
  • We report the first case of a diagnosis of an asymptomatic primary renal angiosarcoma.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Hemangiosarcoma / surgery. Incidental Findings. Kidney Neoplasms / diagnosis. Kidney Neoplasms / surgery

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  • [CommentIn] Int J Urol. 2007 Aug;14(8):777; author reply 777-8 [17681076.001]
  • (PMID = 16903939.001).
  • [ISSN] 0919-8172
  • [Journal-full-title] International journal of urology : official journal of the Japanese Urological Association
  • [ISO-abbreviation] Int. J. Urol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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38. Lahat G, Dhuka AR, Hallevi H, Xiao L, Zou C, Smith KD, Phung TL, Pollock RE, Benjamin R, Hunt KK, Lazar AJ, Lev D: Angiosarcoma: clinical and molecular insights. Ann Surg; 2010 Jun;251(6):1098-106
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  • [Title] Angiosarcoma: clinical and molecular insights.
  • OBJECTIVE: Angiosarcoma (AS) is a rare understudied soft tissue sarcoma exhibiting endothelial cell differentiation.
  • RESULTS: Forty-three (19.4%) metastatic AS patients and 179 patients (80.6%) with localized disease were included.
  • Median survival of localized versus metastatic AS was 49 (range, 2-188) versus 10 (range, 1-69) months (P < 0.0001).
  • [MeSH-major] Hemangiosarcoma / mortality

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  • (PMID = 20485141.001).
  • [ISSN] 1528-1140
  • [Journal-full-title] Annals of surgery
  • [ISO-abbreviation] Ann. Surg.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / R01 CA138345
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Adaptor Proteins, Signal Transducing; 0 / Benzamides; 0 / Biomarkers, Tumor; 0 / DNA-Binding Proteins; 0 / EIF4EBP1 protein, human; 0 / ELF4 protein, human; 0 / Phosphoproteins; 0 / Transcription Factors; 0 / Vascular Endothelial Growth Factor A; 82558-50-7 / isoxaben; EC 2.7.- / Phosphotransferases; EC 2.7.10.1 / Proto-Oncogene Proteins c-kit; EC 2.7.10.1 / Receptor, Epidermal Growth Factor; EC 2.7.11.1 / Proto-Oncogene Proteins c-akt
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39. Eng SP, Goh CH, Khoo JB, Yang TL, Lim LH: Metastatic angiosarcoma to the thyroid. Rev Laryngol Otol Rhinol (Bord); 2005;126(2):111-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metastatic angiosarcoma to the thyroid.
  • BACKGROUND: Angiosarcoma (AS) in non-alpine areas is exceptionally rare, and so is metastatic AS to the thyroid.
  • RESULTS: A Chinese gentleman with AS metastatic to the thyroid presented a year after radiotherapy to his scalp AS.
  • CONCLUSION: AS metastatic to the thyroid is possible.
  • [MeSH-major] Hemangiosarcoma / secondary. Thyroid Neoplasms / secondary

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  • (PMID = 16180351.001).
  • [ISSN] 0035-1334
  • [Journal-full-title] Revue de laryngologie - otologie - rhinologie
  • [ISO-abbreviation] Rev Laryngol Otol Rhinol (Bord)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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40. Quesenberry CD, Li C, Chen AH, Zweizig SL, Ball HG 3rd: Primary angiosarcoma of the ovary: a case report of Stage I disease. Gynecol Oncol; 2005 Oct;99(1):218-21
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the ovary: a case report of Stage I disease.
  • BACKGROUND: There are 20 documented cases of primary ovarian angiosarcoma.
  • Most patients present with metastatic disease and respond poorly to chemotherapy.
  • CASE: We present a case of Stage Ic primary ovarian angiosarcoma treated with 3 cycles of adjuvant MAID chemotherapy.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Hemangiosarcoma / drug therapy. Ovarian Neoplasms / drug therapy

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  • (PMID = 16081151.001).
  • [ISSN] 0090-8258
  • [Journal-full-title] Gynecologic oncology
  • [ISO-abbreviation] Gynecol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 7GR28W0FJI / Dacarbazine; 80168379AG / Doxorubicin; NR7O1405Q9 / Mesna; UM20QQM95Y / Ifosfamide; MAID protocol
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41. Arribas-Garcia I, Domínguez MF, Alcalá-Galiano A, García AF, Valls JC, De Rasche EN: Oral primary angiosarcoma of the lower lip mucosa: report of a case in a 15-year-old boy. Head Neck; 2008 Oct;30(10):1384-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Oral primary angiosarcoma of the lower lip mucosa: report of a case in a 15-year-old boy.
  • METHODS AND RESULTS: We present the case of an inferior lip mucosal low-grade angiosarcoma in a 15-year-old boy treated exclusively with surgery.
  • [MeSH-major] Hemangiosarcoma. Lip Neoplasms

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  • [Copyright] Copyright (c) 2008 Wiley Periodicals, Inc. Head Neck 2008.
  • (PMID = 18286486.001).
  • [ISSN] 1097-0347
  • [Journal-full-title] Head & neck
  • [ISO-abbreviation] Head Neck
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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42. Uchiyama Y, Murakami S, Kishino M, Furukawa S: A case report of primary gingival angiosarcoma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Dec;108(6):e17-21

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case report of primary gingival angiosarcoma.
  • Angiosarcoma is a rare malignant neoplasm and primary angiosarcoma is extremely rare.
  • This study reports clinico-pathological features and CT image finding of a case of primary angiosarcoma in the upper gingival and a review of previously reported cases of primary gingival angiosarcomas including the present case.
  • [MeSH-major] Gingival Neoplasms / pathology. Hemangiosarcoma / pathology. Maxillary Neoplasms / pathology

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  • (PMID = 19913715.001).
  • [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; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Interleukin-2; 0 / Recombinant Proteins
  • [Number-of-references] 12
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43. Gatcombe HG, Olson TA, Esiashvili N: Metastatic primary angiosarcoma of the breast in a pediatric patient with a complete response to systemic chemotherapy and definitive radiation therapy: case report and review of the literature. J Pediatr Hematol Oncol; 2010 Apr;32(3):192-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metastatic primary angiosarcoma of the breast in a pediatric patient with a complete response to systemic chemotherapy and definitive radiation therapy: case report and review of the literature.
  • We present a case of a rare malignancy, primary breast angiosarcoma, in a 15-year-old girl.
  • She presented with a locally advanced tumor and suspected metastatic disease to the mediastinum and bones on PET imaging.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Bone Neoplasms / therapy. Breast Neoplasms / therapy. Hemangiosarcoma / therapy. Mediastinal Neoplasms / therapy. Radiotherapy

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  • (PMID = 20186104.001).
  • [ISSN] 1536-3678
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 5J49Q6B70F / Vincristine; 80168379AG / Doxorubicin; UM20QQM95Y / Ifosfamide
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44. 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

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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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45. Liu ZH, Lee ST, Jung SM, Tu PH: Primary spinal angiosarcoma. J Clin Neurosci; 2010 Mar;17(3):387-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary spinal angiosarcoma.
  • Primary angiosarcoma of the spine is rare.
  • To our knowledge, primary angiosarcoma in the posterior element of the spine has not been reported previously.
  • [MeSH-major] Hemangiosarcoma. Spinal Neoplasms

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  • [Copyright] Copyright 2009 Elsevier Ltd. All rights reserved.
  • (PMID = 20074966.001).
  • [ISSN] 1532-2653
  • [Journal-full-title] Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
  • [ISO-abbreviation] J Clin Neurosci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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46. Hasiloglu ZI, Metin DY, Ozbayrak M, Havan N: Locally invasive primary splenic angiosarcoma. Eurasian J Med; 2010 Dec;42(3):160-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Locally invasive primary splenic angiosarcoma.
  • Primary angiosarcoma of the spleen is a very rare vascular neoplasm, but it represents the most common non-hematolymphoid malignant tumor of the spleen.
  • In this report, we present the case of a 48-year-old man with primary splenic angiosarcoma with local invasion to the left diaphragm and the radiological imaging findings for this cancer.

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  • (PMID = 25610150.001).
  • [ISSN] 1308-8734
  • [Journal-full-title] The Eurasian journal of medicine
  • [ISO-abbreviation] Eurasian J Med
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Turkey
  • [Other-IDs] NLM/ PMC4299831
  • [Keywords] NOTNLM ; Computed tomography / Neoplasm / Splenic angiosarcoma
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47. Thompson WM, Levy AD, Aguilera NS, Gorospe L, Abbott RM: Angiosarcoma of the spleen: imaging characteristics in 12 patients. Radiology; 2005 Apr;235(1):106-15

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

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  • [Copyright] (c) RSNA, 2005
  • (PMID = 15749977.001).
  • [ISSN] 0033-8419
  • [Journal-full-title] Radiology
  • [ISO-abbreviation] Radiology
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, U.S. Gov't, Non-P.H.S.
  • [Publication-country] United States
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48. Penel N, Bui BN, Bay JO, Cupissol D, Ray-Coquard I, Piperno-Neumann S, Kerbrat P, Fournier C, Taieb S, Jimenez M, Isambert N, Peyrade F, Chevreau C, Bompas E, Brain EG, Blay JY: Phase II trial of weekly paclitaxel for unresectable angiosarcoma: the ANGIOTAX Study. J Clin Oncol; 2008 Nov 10;26(32):5269-74
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Phase II trial of weekly paclitaxel for unresectable angiosarcoma: the ANGIOTAX Study.
  • PURPOSE: The objective of this phase II trial was to assess the efficacy and toxicity of weekly paclitaxel for patients with metastatic or unresectable angiosarcoma.
  • The primary end point was the nonprogression rate after two cycles.
  • Three patients with locally advanced breast angiosarcoma presented partial response, which enabled a secondary curative-intent surgery with complete histologic response in two cases.
  • [MeSH-major] Antineoplastic Agents, Phytogenic / administration & dosage. Breast Neoplasms / drug therapy. Head and Neck Neoplasms / drug therapy. Hemangiosarcoma / drug therapy. Paclitaxel / administration & dosage. Scalp. Skin Neoplasms / drug therapy. Soft Tissue Neoplasms / drug therapy

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  • (PMID = 18809609.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Clinical Trial, Phase II; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents, Phytogenic; P88XT4IS4D / Paclitaxel
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49. Yoshida K, Ito F, Nakazawa H, Maeda Y, Tomoe H, Aiba M: A case of primary renal angiosarcoma. Rare Tumors; 2009;1(2):e28

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case of primary renal angiosarcoma.
  • The renal specimen was re-evaluated using whole cross-section analysis and immunohistochemistry, and diagnosed as a primary renal angiosarcoma.
  • Recombinant interleukin-2 therapy was started immediately; however, the patient died of metastatic disease 13 months after the initial operation.
  • Although contrast imaging depicted the primary lesion as a non-specific hematoma with little focal pooling, and low-grade cytological atypia was shown pathologically, the angiosarcoma was extremely aggressive.

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  • (PMID = 21139907.001).
  • [ISSN] 2036-3613
  • [Journal-full-title] Rare tumors
  • [ISO-abbreviation] Rare Tumors
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Italy
  • [Other-IDs] NLM/ PMC2994470
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50. Di Tommaso L, Colombo G, Miceli S, Ferrari B, Santoro A, Poletti A, Roncalli M: [Angiosarcoma of the nasal cavity. Report of a case and review of the literature]. Pathologica; 2007 Jun;99(3):76-80
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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 nasal cavity. Report of a case and review of the literature].
  • [Transliterated title] Angiosarcoma della cavità nasale. Descrizione di un caso e revisione della letteratura.
  • We report an unusual case of primary angiosarcoma of the nasal cavity (AS-nc).
  • [MeSH-major] Hemangiosarcoma / pathology. Nasal Cavity. Nose Neoplasms / pathology

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  • (PMID = 17987727.001).
  • [ISSN] 0031-2983
  • [Journal-full-title] Pathologica
  • [ISO-abbreviation] Pathologica
  • [Language] ita
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Italy
  • [Number-of-references] 10
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51. Souza FF, Katkar A, den Abbeele AD, Dipiro PJ: Breast angiosarcoma metastatic to the ovary. Case Rep Med; 2009;2009:381015
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Breast angiosarcoma metastatic to the ovary.
  • Approximately 5%-10% of ovarian malignancies are diagnosed as metastatic tumors.
  • Primary angiosarcoma can arise anywhere in the body and when it arises in the breast, it usually affects women in their 3rd and 4th decades and accounts for one in 1700-2300 cases of primary breast cancer.
  • We present a case of a solitary ovarian metastasis from angiosarcoma of the breast.

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  • (PMID = 19718246.001).
  • [ISSN] 1687-9627
  • [Journal-full-title] Case reports in medicine
  • [ISO-abbreviation] Case Rep Med
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2729273
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52. Safapor F, Aghajanzade M, Kohsari MR, Hoda S, Safarpor D: Spontaneous rupture of the spleen: a case report and review of the literature. Saudi J Gastroenterol; 2007 Jul-Sep;13(3):136-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Primary angiosarcoma of the spleen is a very rare neoplasm with disastrous prognosis.

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  • (PMID = 19858631.001).
  • [ISSN] 1998-4049
  • [Journal-full-title] Saudi journal of gastroenterology : official journal of the Saudi Gastroenterology Association
  • [ISO-abbreviation] Saudi J Gastroenterol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Saudi Arabia
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53. 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].
  • [Transliterated title] Angiosarcome mammaire primitif: à propos de deux cas.
  • 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

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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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54. Delacruz V, Jorda M, Gomez-Fernandez C, Benedetto P, Ganjei P: Fine-needle aspiration diagnosis of angiosarcoma of the spleen: a case report and review of the literature. Arch Pathol Lab Med; 2005 Aug;129(8):1054-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Fine-needle aspiration diagnosis of angiosarcoma of the spleen: a case report and review of the literature.
  • Primary angiosarcoma of the spleen is a very rare neoplasm with a poor prognosis.
  • We describe a case of angiosarcoma diagnosed by fine-needle aspiration cytology prior to splenectomy.
  • A malignant endothelial neoplasm was diagnosed by fine-needle aspiration cytology using immunocytochemistry, and a splenectomy confirmed the presence of angiosarcoma.
  • To our knowledge, this is the first well-documented and confirmed case of primary angiosarcoma of the spleen diagnosed by fine-needle aspiration cytology.
  • [MeSH-major] Biopsy, Fine-Needle. Hemangiosarcoma / secondary. Splenic Neoplasms / pathology
  • [MeSH-minor] Aged. Antigens, CD31 / analysis. Biomarkers, Tumor / analysis. Endothelium, Vascular / chemistry. Endothelium, Vascular / pathology. Factor VIII / analysis. Female. Humans. Immunohistochemistry. Liposarcoma / chemistry. Liposarcoma / pathology. Liposarcoma / surgery. Neoplasms, Multiple Primary. Spleen / pathology. Spleen / radiography. Spleen / surgery. Splenectomy. Tomography, X-Ray Computed. Treatment Outcome

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  • (PMID = 16048401.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD31; 0 / Biomarkers, Tumor; 9001-27-8 / Factor VIII
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55. 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

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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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56. den Hoed ID, Granzen B, Granzen B, Aronson DC, Pauwels P, de Kraker J, van Heurn LW: Metastasized angiosarcoma of the spleen in a 2-year-old girl. Pediatr Hematol Oncol; 2005 Jul-Aug;22(5):387-90
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metastasized angiosarcoma of the spleen in a 2-year-old girl.
  • Primary angiosarcoma of the spleen is rare and the prognosis is very poor.
  • The authors present a 2-year-old girl with spontaneous rupture of splenic angiosarcoma.
  • [MeSH-major] Hemangiosarcoma / secondary. Liver Neoplasms / secondary. Splenic Neoplasms / pathology

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  • (PMID = 16020128.001).
  • [ISSN] 0888-0018
  • [Journal-full-title] Pediatric hematology and oncology
  • [ISO-abbreviation] Pediatr Hematol Oncol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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57. Jobke B, Werner M, Jundt G, Ostertag H, Freyschmidt J: Protracted disseminated skeletal metastases from angiosarcoma of the spleen. Clin Exp Metastasis; 2010 Feb;27(2):117-22
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Protracted disseminated skeletal metastases from angiosarcoma of the spleen.
  • The 55-years-old patient presented in this case report had a disease-free 4 years interval between splenectomy after primary angiosarcoma of the spleen and an unusual skeletal metastatic pattern mimicking benign angiomatosis.
  • Despite lacking radiographic evidence for a highly aggressive osseous process, the histopathological resemblance of the bone biopsy with the primary tumor manifestation and the fulminant course of disease after onset of disseminated osseous spread confirmed the malignant character of the vascular tumor.
  • [MeSH-major] Bone Neoplasms / secondary. Hemangiosarcoma / pathology. Splenic Neoplasms / pathology

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  • [Cites] Skeletal Radiol. 1996 Apr;25(3):255-61 [8741063.001]
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  • (PMID = 20174857.001).
  • [ISSN] 1573-7276
  • [Journal-full-title] Clinical & experimental metastasis
  • [ISO-abbreviation] Clin. Exp. Metastasis
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Netherlands
  • [Number-of-references] 21
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58. Butrón Vila T, García Villar O, Alonso García S, Bonachia Naranjo O, Pérez Espejo G, Lomas Espadas M, Hidalgo Pascual M: Angiosarcoma in the small intestine. Apropos of a particular case. Hepatogastroenterology; 2005 Jul-Aug;52(64):1139-42
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiosarcoma in the small intestine. Apropos of a particular case.
  • Presentation of a case of small intestine primary angiosarcoma in a 70-year-old male.
  • [MeSH-major] Hemangiosarcoma / pathology. Ileal Neoplasms / pathology

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  • (PMID = 16001647.001).
  • [ISSN] 0172-6390
  • [Journal-full-title] Hepato-gastroenterology
  • [ISO-abbreviation] Hepatogastroenterology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Greece
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59. Ho CK, Wang E, Au WK, Cheng LC: Primary cardiac angiosarcoma of left atrium. J Card Surg; 2009 Sep-Oct;24(5):524-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary cardiac angiosarcoma of left atrium.
  • Cardiac angiosarcoma usually arises from the right atrium.
  • We report an extremely rare case of primary angiosarcoma originating from the left atrium in a 70-year-old woman.
  • This represents the ninth reported case of left-sided cardiac angiosarcoma in the English literature.
  • [MeSH-major] Heart Atria / pathology. Heart Neoplasms / pathology. Hemangiosarcoma / pathology

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  • (PMID = 19740289.001).
  • [ISSN] 1540-8191
  • [Journal-full-title] Journal of cardiac surgery
  • [ISO-abbreviation] J Card Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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60. Pace V, Wieczorek G, Pace M, Weber K, Perentes E: Spontaneous metastatic angiosarcoma of the tongue in a Wistar rat: morphological and immunohistochemical characterization. Toxicol Pathol; 2010 Apr;38(3):472-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Spontaneous metastatic angiosarcoma of the tongue in a Wistar rat: morphological and immunohistochemical characterization.
  • A primary angiosarcoma was found in the tongue of a six-week-old female Wistar rat, sacrificed for humane reasons during the course of a four-week toxicology study.
  • Multiple metastases were found in the lungs, and the morphology of the cells resembled that of the primary tumor.
  • Immunohistochemically, the primary tumor and the lung metastases were positive for von Willebrand factor and vimentin.
  • The diagnosis of tongue angiosarcoma metastasizing to the lungs was made on the basis of microscopic and immunohistochemical findings.
  • [MeSH-major] Hemangiosarcoma / secondary. Hemangiosarcoma / veterinary. Lung Neoplasms / secondary. Lung Neoplasms / veterinary. Tongue Neoplasms / pathology. Tongue Neoplasms / veterinary

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  • (PMID = 20215585.001).
  • [ISSN] 1533-1601
  • [Journal-full-title] Toxicologic pathology
  • [ISO-abbreviation] Toxicol Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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61. Sadhu S, Pattari S, Shaikh F, Verma R, Roy MK: Colonic metastasis from subcutaneous angiosarcoma: A diagnostic dilemma. Indian J Surg; 2010 Jul;72(Suppl 1):328-30

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Colonic metastasis from subcutaneous angiosarcoma: A diagnostic dilemma.
  • Primary angiosarcoma is an extremely rare and aggressive soft-tissue malignancy of endothelial cell origin that occurs most frequently in the skin and subcutaneous tissues of the extremities.
  • Presence of this disease in the intestine as a primary or metastatic deposit is an extremely uncommon incident, and might causes diagnostic confusion with primary colonic neoplasm.
  • We encountered epithelioid angiosarcoma of the sigmoid colon in a 59-year-old male patient who presented with occasional bleeding per rectum and had also had an angiosarcoma arising from the subcutaneous tissue of the right thigh.

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  • [Cites] Am J Surg Pathol. 1998 Jun;22(6):683-97 [9630175.001]
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  • (PMID = 23133287.001).
  • [ISSN] 0972-2068
  • [Journal-full-title] The Indian journal of surgery
  • [ISO-abbreviation] Indian J Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC3451850
  • [Keywords] NOTNLM ; Angiosarcoma / Colonic metastasis
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62. Park SM, Kang WC, Park CH, Shin MS, Chung WJ, Ahn TH, Shin EK: Rapidly growing angiosarcoma of the pericardium presenting as hemorrhagic pericardial effusion. Int J Cardiol; 2008 Oct 30;130(1):109-12

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rapidly growing angiosarcoma of the pericardium presenting as hemorrhagic pericardial effusion.
  • Primary angiosarcoma of the heart is exceptionally rare.
  • Angiosarcoma of the heart often go undetected until late in the course of the disease as symptoms are insidious and available non-invasive imaging modalities lack specificity.
  • Recently, we experienced an angiosarcoma of the pericardium that presented hemorrhagic pericardial effusion initially, but progressed rapidly during short period.
  • [MeSH-major] Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis. Pericardium

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  • (PMID = 18082279.001).
  • [ISSN] 1874-1754
  • [Journal-full-title] International journal of cardiology
  • [ISO-abbreviation] Int. J. Cardiol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Netherlands
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63. 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.
  • [MeSH-major] Ascites / pathology. Cytodiagnosis / methods. Hemangiosarcoma / pathology. Ovarian Neoplasms / pathology

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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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64. Pfeiffer DF, Bode-Lesniewska B: Fine needle aspiration biopsy diagnosis of angiosarcoma after breast-conserving therapy for carcinoma supported by use of a cell block and immunohistochemistry. Acta Cytol; 2006 Sep-Oct;50(5):553-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Fine needle aspiration biopsy diagnosis of angiosarcoma after breast-conserving therapy for carcinoma supported by use of a cell block and immunohistochemistry.
  • BACKGROUND: Angiosarcoma is a rare malignant soft tissue tumor occurring at various sites as either a primary or secondary event.
  • Primary angiosarcoma of the breast is an unusual tumor, counting for 1 in 1700-2,000 primary malignant tumors of this organ.
  • CASE: Angiosarcoma arose 6 years after breast-conserving therapy for invasive carcinoma in a 69-year-old woman.
  • Fine needle aspiration of several small, reddish, intradermal nodules over the treated area revealed malignant cells with an endothelial immunophenotype in the cel block, yielding the diagnosis of angiosarcoma, subsequently confired in a mastectomy speciman.
  • CONCLUSION: Fine needle aspiration, supported by ancillary techniques, such as cell block and immunohistochemistry, allows the cytologic diagnosis of an angiosarcoma and differentiates it from a carcinoma recurrence.
  • [MeSH-major] Breast / pathology. Breast Neoplasms / diagnosis. Carcinoma, Ductal, Breast / diagnosis. Hemangiosarcoma / diagnosis. Neoplasms, Second Primary / diagnosis. Radiotherapy / adverse effects

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  • (PMID = 17017445.001).
  • [ISSN] 0001-5547
  • [Journal-full-title] Acta cytologica
  • [ISO-abbreviation] Acta Cytol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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65. Kunkel T, Mylonas I, Mayr D, Friese K, Sommer HL: Recurrence of secondary angiosarcoma in a patient with post-radiated breast for breast cancer. Arch Gynecol Obstet; 2008 Nov;278(5):497-501
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Recurrence of secondary angiosarcoma in a patient with post-radiated breast for breast cancer.
  • INTRODUCTION: Angiosarcoma of the breast is a rare finding.
  • Two different subtypes of angiosarcomas have been described: (a) the Stewart-Treves syndrome and (b) the cutaneous post-radiation angiosarcoma.
  • We report a case where both types of angiosarcoma occurred.
  • CASE REPORT: At first, an angiosarcoma affecting parenchyma of the breast was observed after radiotherapy following breast conserving therapy and a history of lymphoedema of the radiated area.
  • Additionally, a subsequent local recurrence of the angiosarcoma of the skin after mastectomy and complete resection of the primary angiosarcoma was diagnosed.
  • DISCUSSION: This case is distinguished by a short latency period after primary therapy (less than 4 years) and a rapid recurrence after complete resection (14 weeks).
  • Additionally, every oncologist should be aware of this rare complication as quick diagnosis and prompt surgical treatment is indispensable due to the aggressive entity of angiosarcoma.
  • [MeSH-major] Breast Neoplasms / therapy. Hemangiosarcoma / therapy. Neoplasm Recurrence, Local / therapy. Skin Neoplasms / therapy

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  • (PMID = 18305948.001).
  • [ISSN] 0932-0067
  • [Journal-full-title] Archives of gynecology and obstetrics
  • [ISO-abbreviation] Arch. Gynecol. Obstet.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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66. Kinderyte R, Alisauskaite L, Juodzbaliene EB, Juozaityte E: [Angiosarcoma of the breast: a case report and literature review]. Medicina (Kaunas); 2006;42(7):580-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Angiosarcoma of the breast: a case report and literature review].
  • In literature, only isolated cases of primary angiosarcoma of the breast were described.
  • 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

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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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67. Husted TL, Neff G, Thomas MJ, Gross TG, Woodle ES, Buell JF: Liver transplantation for primary or metastatic sarcoma to the liver. Am J Transplant; 2006 Feb;6(2):392-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Liver transplantation for primary or metastatic sarcoma to the liver.
  • Sarcoma is generally a rare disease in the US, with poor survival in patients with both primary angiosarcoma and metastatic disease from sarcoma and GIST.
  • Those patients with liver failure from primary or metastatic liver sarcoma were evaluated.
  • 19 patients are identified having received liver transplantation after treatment for sarcoma of the liver, 6 patients with primary hepatic sarcoma and 13 patients with metastatic sarcoma of the liver.
  • Given the early recurrence of tumor and meager 1-year survival outcome, liver transplantation is a poor therapeutic choice for patients with either primary or metastatic liver sarcoma, including high-grade leiomyosarcoma (GIST) regardless of primary site or primary therapy.


68. Fontanesi J, Mott MP, Kraut MJ, Lucas DR, Miller PR: A unique radiation scheme for the treatment of high-grade non-metastatic soft tissue sarcoma: the detroit medical center experience. Sarcoma; 2005;9(3-4):141-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A unique radiation scheme for the treatment of high-grade non-metastatic soft tissue sarcoma: the detroit medical center experience.
  • PURPOSE: This is the initial report on the utilization of combined photon irradiation followed by a neutron boost irradiation for the initial management of patients with high-grade non-metastatic soft tissue sarcoma (STS).
  • METHODS AND MATERIALS: Between 1/1/1995 and 10/31/02, twenty-three patients with high-grade non-metastatic soft tissue sarcoma were referred to the Department of Radiation Oncology at the Detroit Medical Center.
  • The most common histology was malignant fibrous histiocytoma (n=6), followed by liposarcoma (n=5), synovial sarcoma (n=4), and angiosarcoma (n=2).

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  • (PMID = 18521422.001).
  • [ISSN] 1357-714X
  • [Journal-full-title] Sarcoma
  • [ISO-abbreviation] Sarcoma
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Egypt
  • [Other-IDs] NLM/ PMC2395635
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69. Balamurali G, du Plessis DG, Wengoy M, Bryan N, Herwadkar A, Richardson PL: Thorotrast-induced primary cerebral angiosarcoma: case report. Neurosurgery; 2009 Jul;65(1):E210-1; discussion E211
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Thorotrast-induced primary cerebral angiosarcoma: case report.
  • Gliosarcomas, meningiomas, and schwannomas have been reported previously, as has Thorotrast-associated angiosarcoma, typically in the liver.
  • A unique case of a primary intracerebral well-differentiated angiosarcoma in a 68-year-old man with a history of colocalized exposure to Thorotrast is described.
  • This may be the first case of a primary angiosarcoma in the brain.
  • Primary lesions of the central nervous system associated with Thorotrast are very rarely reported, despite its extensive use in cerebral angiography and management of brain abscess between 1930 and 1960.
  • [MeSH-major] Brain Neoplasms / chemically induced. Carcinogens / pharmacology. Hemangiosarcoma / chemically induced. Hemangiosarcoma / diagnosis. Thorium Dioxide / pharmacology

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  • (PMID = 19574803.001).
  • [ISSN] 1524-4040
  • [Journal-full-title] Neurosurgery
  • [ISO-abbreviation] Neurosurgery
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Carcinogens; 9XA7X17UQC / Thorium Dioxide
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70. Biswas T, Tang P, Muhs A, Ling M: Angiosarcoma of the breast: a rare clinicopathological entity. Am J Clin Oncol; 2009 Dec;32(6):582-6
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  • [Title] Angiosarcoma of the breast: a rare clinicopathological entity.
  • OBJECTIVES: Angiosarcoma is a rare subtype of sarcoma that usually arises after radiation therapy for primary breast cancer.
  • Primary sarcomas of the breast are rare entities and account for less than 1% of all malignant breast neoplasms.
  • METHODS: To conduct a retrospective review, all female patients with a diagnosis of angiosarcoma of the breast were identified from our pathology database.
  • RESULTS: A total of 8 patients were identified who had a histologically confirmed diagnosis of angiosarcoma of the breast.
  • Seven (87%) patients had a history of prior radiation to the breast, whereas 1 (13%) had primary angiosarcoma.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology. Neoplasms, Radiation-Induced / pathology. Neoplasms, Second Primary / pathology

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  • (PMID = 19581792.001).
  • [ISSN] 1537-453X
  • [Journal-full-title] American journal of clinical oncology
  • [ISO-abbreviation] Am. J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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71. Vorburger SA, Xing Y, Hunt KK, Lakin GE, Benjamin RS, Feig BW, Pisters PW, Ballo MT, Chen L, Trent J 3rd, Burgess M, Patel S, Pollock RE, Cormier JN: Angiosarcoma of the breast. Cancer; 2005 Dec 15;104(12):2682-8
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  • [Title] Angiosarcoma of the breast.
  • BACKGROUND: Angiosarcoma of the breast is a rare entity.
  • METHODS: Clinical and pathologic factors were analyzed in all patients with angiosarcoma of the breast treated between 1990 and 2003.
  • RESULTS: Fifty-five women with angiosarcoma of the breast were identified.
  • For the 32 patients with primary angiosarcoma of the breast 5-year OS was 59%.
  • These patients with radiation therapy-associated angiosarcoma were on average 30 years older and less likely to present with distant metastatic disease than patients presenting with radiation-naive angiosarcoma of the breast.
  • CONCLUSIONS: In this series of 55 patients with angiosarcoma of the breast, radiation therapy-naive angiosarcomas occurred in younger patients, but they behaved similarly to radiation therapy-associated angiosarcomas.
  • [MeSH-major] Breast Neoplasms / mortality. Breast Neoplasms / therapy. Hemangiosarcoma / mortality. Hemangiosarcoma / therapy. Mastectomy / methods

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  • [Copyright] Copyright 2005 American Cancer Society.
  • (PMID = 16288486.001).
  • [ISSN] 0008-543X
  • [Journal-full-title] Cancer
  • [ISO-abbreviation] Cancer
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
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72. Gambino G, Mannone T, Rizzo A, Scio A, Branca M, Airò Farulla M, Guccione M, Spallitta IS, Nicoli N: Adrenal epithelioid angiosarcoma: a case report. Chir Ital; 2008 May-Jun;60(3):463-7
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  • [Title] Adrenal epithelioid angiosarcoma: a case report.
  • We report what to the best of our knowledge is the first case of primary angiosarcoma of the adrenal gland.
  • [MeSH-major] Adrenal Gland Neoplasms. Hemangiosarcoma

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  • (PMID = 18709789.001).
  • [ISSN] 0009-4773
  • [Journal-full-title] Chirurgia italiana
  • [ISO-abbreviation] Chir Ital
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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73. de Keizer RJ, de Wolff-Rouendaal D, Nooy MA: Angiosarcoma of the eyelid and periorbital region. Experience in Leiden with iridium192 brachytherapy and low-dose doxorubicin chemotherapy. Orbit; 2008;27(1):5-12
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  • [Title] Angiosarcoma of the eyelid and periorbital region. Experience in Leiden with iridium192 brachytherapy and low-dose doxorubicin chemotherapy.
  • AIM: To report on the use of iridium(192) brachytherapy and doxorubicin chemotherapy as adjuvant therapy in 6 patients with angiosarcoma of the eyelid and periorbital region.
  • MATERIAL AND METHODS: Tumor localization and diameter, signs of inflammation, histology and treatment are discussed in this retrospective study of 6 patients (age 46-87 yrs.) presenting with primary angiosarcoma in the eyelid.
  • RESULTS: Six patients (4 elderly) with angiosarcoma localized in one or more eyelids, the face or multilocular were seen between 1987 and 2000.
  • CONCLUSION: If radical surgery for angiosarcoma of the eyelid and periorbital region is not possible, adjuvant iridium(192) wire brachytherapy may prove beneficial.
  • [MeSH-major] Eyelid Neoplasms / therapy. Hemangiosarcoma / therapy. Orbital Neoplasms / therapy

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  • (PMID = 18307140.001).
  • [ISSN] 1744-5108
  • [Journal-full-title] Orbit (Amsterdam, Netherlands)
  • [ISO-abbreviation] Orbit
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antibiotics, Antineoplastic; 0 / Iridium Radioisotopes; 0 / Radiopharmaceuticals; 80168379AG / Doxorubicin
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74. Wang XY, Jakowski J, Tawfik OW, Thomas PA, Fan F: Angiosarcoma of the breast: a clinicopathologic analysis of cases from the last 10 years. Ann Diagn Pathol; 2009 Jun;13(3):147-50
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  • [Title] Angiosarcoma of the breast: a clinicopathologic analysis of cases from the last 10 years.
  • Breast angiosarcoma may occur de novo, or as a complication of radiation therapy, or chronic lymphedema secondary to axillary lymph node dissection for mammary carcinoma.
  • In our effort to characterize the clinicopathologic features of breast angiosarcoma, we reviewed all breast angiosarcoma cases in the University of Kansas Medical Center and Ohio State University Medical Center archives from 1997 to 2007.
  • Eight cases (6 high grade, 1 intermediate grade, 1 low grade) were identified as postradiation angiosarcoma (postradiation time interval, 4-12 years), and 3 cases were identified as primary angiosarcomas (1 high grade, 2 low grade).
  • Follow-up (median, 36 months) revealed that 3 cases of postradiation angiosarcoma recurred as skin and/or chest wall lesions and 1 case of primary angiosarcoma developed liver metastases (all high-grade).
  • In conclusion, breast angiosarcoma remains a rare disease.
  • Rosen's method for grading breast angiosarcoma is easy to implement and correlates well with clinical outcome.
  • There are no distinct clinical or histologic differences between primary and postradiation breast angiosarcomas.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology

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  • (PMID = 19433291.001).
  • [ISSN] 1532-8198
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 12
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75. Maki RG, D'Adamo DR, Keohan ML, Saulle M, Schuetze SM, Undevia SD, Livingston MB, Cooney MM, Hensley ML, Mita MM, Takimoto CH, Kraft AS, Elias AD, Brockstein B, Blachère NE, Edgar MA, Schwartz LH, Qin LX, Antonescu CR, Schwartz GK: Phase II study of sorafenib in patients with metastatic or recurrent sarcomas. J Clin Oncol; 2009 Jul 01;27(19):3133-40
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  • [Title] Phase II study of sorafenib in patients with metastatic or recurrent sarcomas.
  • PURPOSE Since activity of sorafenib was observed in sarcoma patients in a phase I study, we performed a multicenter phase II study of daily oral sorafenib in patients with recurrent or metastatic sarcoma.
  • In each arm, 12 patients who received 0 to 1 prior lines of therapy were treated (0 to 3 for angiosarcoma and malignant peripheral-nerve sheath tumor).
  • Five of 37 patients with angiosarcoma had a partial response (response rate, 14%).
  • This was the only arm to meet the RECIST response rate primary end point.
  • There was no correlation between phosphorylated extracellular signal regulated kinase expression and response in six patients with angiosarcoma with paired pre- and post-therapy biopsies.
  • CONCLUSION As a single agent, sorafenib has activity against angiosarcoma and minimal activity against other sarcomas.

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  • (PMID = 19451436.001).
  • [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
  • [Grant] United States / NCI NIH HHS / CA / N01CM62202; United States / NCI NIH HHS / CA / P01 CA047179
  • [Publication-type] Clinical Trial, Phase II; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Benzenesulfonates; 0 / Phenylurea Compounds; 0 / Pyridines; 25X51I8RD4 / Niacinamide; 9ZOQ3TZI87 / sorafenib
  • [Other-IDs] NLM/ PMC2716936
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76. Liang YM, Li XH, Lü YL, Zhong M: [Morphology and immunohistochemical characteristics of hepatic primary and metastatic malignant spindle cell tumors]. Zhonghua Yi Xue Za Zhi; 2005 Jan 12;85(2):96-100
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  • [Title] [Morphology and immunohistochemical characteristics of hepatic primary and metastatic malignant spindle cell tumors].
  • OBJECTIVE: To investigate the morphology and immunohistochemical characteristics of hepatic primary and metastatic malignant spindle cell tumors, and to conclude the diagnostic and differential diagnostic criteria for these morphologically similar tumors.
  • 20 primary tumors (43.4%), including 3 cases of sarcomatoid carcinoma (6.5%), 11 of angiosarcoma (23.9%), 2 of epithelioid hemangioendothelioma (5%), 1 of spindle cell carcinoid (2.2%), and 3 of undifferentiated sarcoma (6.5%).
  • and 26 metastatic malignant tumors (56.5%), including 20 cases of gastrointestinal stromal tumors (GIST, 43.4%), 3 of leiomyosarcoma (6.5%), 2 of malignant peripheral never sheath tumor (4.3%), and 1 of meningeal hemangiopericytoma (2.2%), resected during operation or collected during imaging-mediated liver puncture underwent hematoxylin-eosin staining, SP staining, and EnVision immunohistochemical staining.
  • RESULTS: Either primary or metastatic tumors showed extensive overlapping in histopathologic appearance, and hemangiopericytoma-like structure was the predominant pattern, which could be seen in nearly every kind of hepatic spindle cell tumors.
  • Most stromal tumor cases were CD117 positive, and existed the condition that the primary tumor was positive and the metastatic tumor was negative or vice versa or one part of specimen was positive but other part was negative.
  • Angiosarcoma and epithelioid hemangioendothelioma expressed different immunoreactivity to CD31, CD34 and factor VIII related antigen.
  • CONCLUSION: Primary angiosarcoma is the most common form of primary spindle cell tumor in liver, and metastatic GIST is predominant in hepatic metastatic spindle cell tumors.
  • [MeSH-major] Carcinoma / pathology. Hemangiosarcoma / pathology. Liver Neoplasms / pathology

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  • (PMID = 15774214.001).
  • [ISSN] 0376-2491
  • [Journal-full-title] Zhonghua yi xue za zhi
  • [ISO-abbreviation] Zhonghua Yi Xue Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / Antigens, CD31; 0 / Antigens, CD34; 0 / Biomarkers, Tumor
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77. Nakamura M, Tsushima K, Yasuo M, Yamazaki Y, Honda T, Koizumi T, Fujimoto K, Kubo K: Angiosarcoma with sacral origin metastasizing to the lung. Intern Med; 2006;45(15):923-6
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  • [Title] Angiosarcoma with sacral origin metastasizing to the lung.
  • Specimens obtained by video-assisted thoracic surgery revealed angiosarcoma, but the primary site of angiosarcoma could not be detected before autopsy.
  • Angiosarcoma is a rare malignant neoplasm with rapid proliferation and they can arise at any region of the body.
  • Angiosarcoma should be included in the different diagnosis of diffuse pulmonary hemorrhage with multiple lung nodules.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Lung Neoplasms / diagnosis. Lung Neoplasms / secondary. Sacrum / pathology. Spinal Neoplasms / diagnosis

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  • (PMID = 16946576.001).
  • [ISSN] 1349-7235
  • [Journal-full-title] Internal medicine (Tokyo, Japan)
  • [ISO-abbreviation] Intern. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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78. Shor S, Helfand SC, Gorman E, Löhr CV: Diagnostic exercise: epithelioid hemangiosarcoma mimicking metastatic prostatic neoplasia in a dog. Vet Pathol; 2009 May;46(3):548-52
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  • [Title] Diagnostic exercise: epithelioid hemangiosarcoma mimicking metastatic prostatic neoplasia in a dog.
  • The diagnosis was metastatic epithelioid hemangiosarcoma, primary site unknown.
  • [MeSH-major] Dog Diseases / pathology. Hemangiosarcoma / veterinary. Prostatic Neoplasms / veterinary

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  • (PMID = 19176508.001).
  • [ISSN] 0300-9858
  • [Journal-full-title] Veterinary pathology
  • [ISO-abbreviation] Vet. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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79. Carnero López B, Fernández Pérez I, Carrasco Alvarez JA, Lázaro Quintela ME, López Jato C, Jorge Fernández M, Gentil González M, Vázquez Tuñas L, Castellanos Díez J: Renal primary angiosarcoma. Clin Transl Oncol; 2007 Dec;9(12):806-10
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  • [Title] Renal primary angiosarcoma.
  • Angiosarcomas account for 2% of all soft tissue sarcomas and of them, primary renal angiosarcomas represent 1%.
  • [MeSH-major] Hemangiosarcoma / pathology. Kidney Neoplasms / pathology

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  • (PMID = 18158986.001).
  • [ISSN] 1699-048X
  • [Journal-full-title] Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
  • [ISO-abbreviation] Clin Transl Oncol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
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80. Magri K, Demoulin G, Millon G, Duvert B: [Metastasis to the breast from non mammary metastasis. Clinical, radiological characteristics and diagnostic process. A report of two cases and a review of literature]. J Gynecol Obstet Biol Reprod (Paris); 2007 Oct;36(6):602-6
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  • [Title] [Metastasis to the breast from non mammary metastasis. Clinical, radiological characteristics and diagnostic process. A report of two cases and a review of literature].
  • The metastatic involvement of the breast from non-mammary neoplasms is a relatively rare condition: 0.5 to 6% of the breast cancers.
  • The search for a primitive tumor is essential, in particular for neuroendocrine carcinoma, stromal sarcoma, and the angiosarcoma which can be primitive tumors of the breast.
  • Treatment is therefore modified, taking into consideration the treatment and prognosis of the primary disease.

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  • (PMID = 17590284.001).
  • [ISSN] 0368-2315
  • [Journal-full-title] Journal de gynécologie, obstétrique et biologie de la reproduction
  • [ISO-abbreviation] J Gynecol Obstet Biol Reprod (Paris)
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Number-of-references] 17
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81. Castaldo ET, Pinson CW: Liver transplantation for non-hepatocellular carcinoma malignancy. HPB (Oxford); 2007;9(2):98-103

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Liver transplantation for non-hepatocellular carcinoma malignancy.
  • LT for other malignancies like cholangiocarcinoma (CCA), hepatoblastoma (HB), hepatic epithelioid hemangioepithelioma (HEHE), angiosarcoma (AS), and neuroendocrine tumors (NET) is being defined.
  • LT plays a role as primary surgical therapy for those individuals in whom tumors remain unresectable after chemotherapy or as rescue therapy for those who are incompletely resected, recur after resection, or develop hepatic insufficiency after chemotherapy and/or resection.
  • For NET, resection of the primary tumor and all gross metastatic disease is reported to provide 5-year survival of 70-85%.

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  • (PMID = 18333123.001).
  • [ISSN] 1365-182X
  • [Journal-full-title] HPB : the official journal of the International Hepato Pancreato Biliary Association
  • [ISO-abbreviation] HPB (Oxford)
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2020792
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82. Valbuena JR, Levenback C, Mansfield P, Liu J: Angiosarcoma of the spleen clinically presenting as metastatic ovarian cancer. A case report and review of the literature. Ann Diagn Pathol; 2005 Oct;9(5):289-92
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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 spleen clinically presenting as metastatic ovarian cancer. A case report and review of the literature.
  • Primary angiosarcomas of the spleen are rare and almost always fatal.
  • The differential diagnosis includes a variety of benign and malignant vascular proliferations (littoral cell angioma and Kaposi's sarcoma) as well as metastatic tumors.
  • We report a case of the 43-year-old woman with a long-standing history of recurrent ovarian carcinoma treated with surgery and multiple courses of radiation therapy and chemotherapy who clinically appeared to have a metastatic ovarian cancer to the spleen and treated with partial resection of stomach and splenectomy.
  • However, histopathologic examination of the specimen showed the tumor to be of a primary angiosarcoma.
  • [MeSH-major] Hemangiosarcoma / pathology. Neoplasms, Second Primary / pathology. Ovarian Neoplasms / pathology. Splenic Neoplasms / pathology


83. Fujii T, Zen Y, Sato Y, Sasaki M, Enomae M, Minato H, Masuda S, Uehara T, Katsuyama T, Nakanuma Y: Podoplanin is a useful diagnostic marker for epithelioid hemangioendothelioma of the liver. Mod Pathol; 2008 Feb;21(2):125-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Podoplanin, which is immunoreactive to D2-40 antibody, is reportedly expressed in lymphatic vessels in non-neoplastic tissues, and also in vascular and non-vascular tumors.
  • However, its expression in non-neoplastic and neoplastic liver tissues has not been well documented.
  • In this study, we examined podoplanin expression in specimens from 10 normal livers and 73 cases of liver tumors: hemangioma (16 cases), epithelioid hemangioendothelioma (9 cases), angiosarcoma (4 cases), angiomyolipoma (7 cases), hepatocellular carcinoma (11 cases), intrahepatic cholangiocarcinoma (11 cases), and metastatic liver cancer (15 cases).
  • The expression of CD31, CD34, and factor VIII was observed in endothelial cells in all cases of hemangioma, epithelioid hemangioendothelioma, angiosarcoma, and angiomyolipoma with one exception, a case of epithelioid hemangioendothelioma which was without CD31 expression.
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Angiomyolipoma / metabolism. Angiomyolipoma / pathology. Bile Duct Neoplasms / metabolism. Bile Duct Neoplasms / pathology. Bile Ducts, Intrahepatic / metabolism. Bile Ducts, Intrahepatic / pathology. Carcinoma, Hepatocellular / metabolism. Carcinoma, Hepatocellular / pathology. Cholangiocarcinoma / metabolism. Cholangiocarcinoma / pathology. Diagnosis, Differential. Endothelium, Lymphatic / metabolism. Endothelium, Lymphatic / pathology. Female. Hemangioma / metabolism. Hemangioma / pathology. Hemangiosarcoma / metabolism. Hemangiosarcoma / pathology. Humans. Liver / metabolism. Liver / pathology. Male. Middle Aged

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  • (PMID = 18084256.001).
  • [ISSN] 0893-3952
  • [Journal-full-title] Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
  • [ISO-abbreviation] Mod. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Membrane Glycoproteins; 0 / PDPN protein, human
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84. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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.
  • A significant number of responses to chemotherapy was observed in the metastatic setting.
  • These data suggest that a multidisciplinary therapeutic approach should be employed in high-risk patients with large primary tumors.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology

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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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85. Simpson L, Kumar SK, Okuno SH, Schaff HV, Porrata LF, Buckner JC, Moynihan TJ: Malignant primary cardiac tumors: review of a single institution experience. Cancer; 2008 Jun;112(11):2440-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Malignant primary cardiac tumors: review of a single institution experience.
  • BACKGROUND: Primary cardiac sarcomas are uncommon.
  • The authors undertook to review the Mayo Clinic's experience with primary cardiac sarcomas consisting of 34 patients seen over a 32-year period.
  • Thirty-four patients with primary cardiac sarcomas were identified and their medical records reviewed for details pertaining to presenting symptoms, staging modalities, treatment approaches, and outcomes.
  • The most common histologic type was angiosarcoma (41%).
  • Patients with angiosarcoma had a lower survival compared with patients with other histologies (5 months vs 17 months; P = .01).
  • The median survival of patients with metastatic disease was 5 months versus 15 months in patients without metastatic disease (P = .03 by the log-rank test).

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  • [Copyright] (c) 2008 American Cancer Society.
  • (PMID = 18428209.001).
  • [ISSN] 1097-0142
  • [Journal-full-title] Cancer
  • [ISO-abbreviation] Cancer
  • [Language] eng
  • [Publication-type] Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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86. Agaimy A, Wünsch PH: Distribution of neural cell adhesion molecule (NCAM/CD56) in gastrointestinal stromal tumours and their intra-abdominal mesenchymal mimics. J Clin Pathol; 2008 Apr;61(4):499-503

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • METHODS: 275 histologically and immunohistochemically well characterised primary and metastatic intra-abdominal mesenchymal lesions were analysed by conventional immunohistochemistry, with emphasis on GIST and GI smooth muscle neoplasms.
  • RESULTS: CD56 expression was seen in 18/21 (86%), 4/5 (80%), 26/34 (76%), and 32/168 (19%) of primary GI leiomyomas, schwannomas, leiomyosarcomas, and GISTs, respectively.
  • Mesenteric fibromatoses, angiosarcoma/Kaposi sarcoma, reactive tumefactive fibrogenic lesions and 12/13 primary anorectal and oesophageal melanomas were negative.
  • CONCLUSION: Results confirmed the ubiquity and non-specificity of CD56 as a neurogenic marker.

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  • (PMID = 17923471.001).
  • [ISSN] 1472-4146
  • [Journal-full-title] Journal of clinical pathology
  • [ISO-abbreviation] J. Clin. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antigens, CD56; 0 / Biomarkers, Tumor; 0 / Neoplasm Proteins
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87. Alvite Canosa M, Alonso Fernández L, Seoane Vigo M, Berdeal Díaz M, Pérez Grobas J, Bouzón Alejandro A, Carral Freire M, de Llano Monelos P, Gómez Freijoso C: [Primary angiosarcoma of the spleen]. Rev Esp Enferm Dig; 2008 Jun;100(6):375-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Primary angiosarcoma of the spleen].
  • [Transliterated title] Angiosarcoma primario de bazo.
  • [MeSH-major] Hemangiosarcoma. Splenic Neoplasms

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  • (PMID = 18752372.001).
  • [ISSN] 1130-0108
  • [Journal-full-title] Revista española de enfermedades digestivas : organo oficial de la Sociedad Española de Patología Digestiva
  • [ISO-abbreviation] Rev Esp Enferm Dig
  • [Language] spa
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Spain
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88. Kiluk JV, Yeh KA: Primary angiosarcoma of the breast. Breast J; 2005 Nov-Dec;11(6):517-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the breast.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology

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  • (PMID = 16297124.001).
  • [ISSN] 1075-122X
  • [Journal-full-title] The breast journal
  • [ISO-abbreviation] Breast J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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89. Tiwary SK, Singh MK, Prasad R, Sharma D, Kumar M, Shukla VK: Primary angiosarcoma of the breast. Surgery; 2007 Jun;141(6):821-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the breast.
  • [MeSH-major] Breast Neoplasms / pathology. Hemangiosarcoma / pathology

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  • (PMID = 17560259.001).
  • [ISSN] 0039-6060
  • [Journal-full-title] Surgery
  • [ISO-abbreviation] Surgery
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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90. Seok JY, Kim YB: [Primary angiosarcoma of the liver]. Korean J Hepatol; 2009 Jun;15(2):216-21
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Primary angiosarcoma of the liver].
  • [MeSH-major] Hemangiosarcoma / pathology. Liver Neoplasms / pathology

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  • (PMID = 19581774.001).
  • [ISSN] 1738-222X
  • [Journal-full-title] The Korean journal of hepatology
  • [ISO-abbreviation] Korean J Hepatol
  • [Language] kor
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Korea (South)
  • [Chemical-registry-number] 0 / Antigens, CD34
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91. Leggio L: Primary angiosarcoma of the kidney: size is the main prognostic factor. Int J Urol; 2007 Aug;14(8):777; author reply 777-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the kidney: size is the main prognostic factor.
  • [MeSH-major] Hemangiosarcoma / pathology. Hemangiosarcoma / surgery. Kidney Neoplasms / pathology. Kidney Neoplasms / surgery

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  • [CommentOn] Int J Urol. 2006 Aug;13(8):1112-4 [16903939.001]
  • (PMID = 17681076.001).
  • [ISSN] 0919-8172
  • [Journal-full-title] International journal of urology : official journal of the Japanese Urological Association
  • [ISO-abbreviation] Int. J. Urol.
  • [Language] eng
  • [Publication-type] Case Reports; Comment; Letter
  • [Publication-country] Australia
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92. 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

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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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93. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Case of the season: primary angiosarcoma of the breast: correlative imaging and pathology.
  • [MeSH-major] Breast Neoplasms / diagnosis. Diagnostic Imaging. Hemangiosarcoma / diagnosis

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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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94. Cammarota G, Schinzari G, Larocca LM, Gasbarrini G, Barone C: Duodenal metastasis from a primary angiosarcoma of the colon. Gastrointest Endosc; 2006 Feb;63(2):330; discussion 330
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Duodenal metastasis from a primary angiosarcoma of the colon.
  • [MeSH-major] Colonic Neoplasms / pathology. Duodenal Neoplasms / secondary. Hemangiosarcoma / secondary

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  • (PMID = 16427950.001).
  • [ISSN] 0016-5107
  • [Journal-full-title] Gastrointestinal endoscopy
  • [ISO-abbreviation] Gastrointest. Endosc.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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95. 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

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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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96. Stamatiou KN, Papadimitriou VD, Takos DM, Heretis IE, Sofras FA: Primary angiosarcoma arising from a multicystic kidney. Saudi Med J; 2008 Jul;29(7):1054-5
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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 arising from a multicystic kidney.
  • [MeSH-major] Hemangiosarcoma / etiology. Hemangiosarcoma / pathology. Kidney Neoplasms / etiology. Kidney Neoplasms / pathology. Multicystic Dysplastic Kidney / pathology

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  • (PMID = 18626542.001).
  • [ISSN] 0379-5284
  • [Journal-full-title] Saudi medical journal
  • [ISO-abbreviation] Saudi Med J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Saudi Arabia
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