Literature DB >> 8279629

Epithelioid angiosarcoma of the adrenal glands. A clinicopathologic study of nine cases with a discussion of the implications of finding "epithelial-specific" markers.

B M Wenig1, S L Abbondanzo, C S Heffess.   

Abstract

Adrenal epithelioid angiosarcomas (AEA) are rare neoplasms. We report the clinicopathologic features of nine cases of AEA. AEA occurred most frequently in the sixth and seventh decades of life (age range, 45-85 years; median, 60); five cases occurred in men and four in women. Presenting symptoms included abdominal mass with or without pain, weight loss, fever, and weakness. Two cases were asymptomatic; one was discovered during evaluation for other disease(s) and the other at autopsy. All neoplasms were nonfunctioning. Radiographic evaluation demonstrated suprarenal or retroperitoneal neoplasms ranging in size from 6 to 10 cm in greatest dimension. Histologically, the neoplasms were invasive, predominantly arranged in solid sheets or nests, and composed of epithelioid cells. Endothelial cell differentiation was suggested by the transition areas between dilated anastomotic vascular spaces and the sheet-like growth, the cytomorphologic similarity between the endothelial cells lining the discernible vascular spaces and those seen in the solid foci, and the presence of intracytoplasmic vacuolization occasionally containing red blood cells. Endothelial derivation was confirmed by immunohistochemistry including Factor VIII-related antigen (FVIII), CD-34 (hematopoetic progenitor cell antigen), and/or Ulex europaeus agglutinin-1 lectin immunoreactivity (UEA-1) and by ultrastructural findings, including rod-shaped microtubulated bodies and intracytoplasmic lumen formation. In addition, cytokeratin reactivity was seen in seven cases, and B72.3 (tumor-associated glycoprotein-72) reactivity was seen in six. Surgical resection was the treatment of choice, occasionally supplemented by chemotherapy. Three patients are presently alive, free of disease, at 13, 11, and 6 years following diagnosis. Three died with metastatic AEA of the lung, and three died of unrelated causes.

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Year:  1994        PMID: 8279629

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  18 in total

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2.  Claudin-5 as an immunohistochemical marker for angiosarcoma and hemangioendotheliomas.

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3.  Primary Adrenal Angiosarcoma: A Rare and Potentially Misdiagnosed Tumor.

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5.  Angiosarcoma of the adrenal gland with concurrent contralateral advanced renal cell carcinoma: A diagnostic and management dilemma.

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6.  Primary epithelioid angiosarcoma of the male breast: report of a case.

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8.  MYC Analysis by Fluorescent In Situ Hybridization and Immunohistochemistry in Primary Adrenal Angiosarcoma (PAA): a Series of Four Cases.

Authors:  Kristine M Cornejo; Lloyd Hutchinson; Maryann St Cyr; Vania Nose; Patrick J McLaughlin; A John Iafrate; Peter M Sadow
Journal:  Endocr Pathol       Date:  2015-12       Impact factor: 3.943

9.  Adrenal Pseudocysts: Evidence of Their Posthemorrhagic Nature.

Authors:  Timothy A. Jennings; Bernard Ng; Ann Boguniewicz; Muzaffar Khan; Donald Rice; James Figge
Journal:  Endocr Pathol       Date:  1998       Impact factor: 3.943

10.  A mimic of sarcomatoid adrenal cortical carcinoma: epithelioid angiosarcoma occurring in adrenal cortical adenoma.

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Journal:  Endocr Pathol       Date:  2014-12       Impact factor: 3.943

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