Literature DB >> 21164288

Primary cutaneous epithelioid angiosarcoma: a clinicopathologic study of 13 cases of a rare neoplasm occurring outside the setting of conventional angiosarcomas and with predilection for the limbs.

Ravi Suchak1, Khin Thway, Bernhard Zelger, Cyril Fisher, Eduardo Calonje.   

Abstract

Epithelioid angiosarcomas are rare aggressive neoplasms that occur most frequently in deep soft tissues. Primary cutaneous lesions are rare, and there are discrepant findings in the literature regarding their behavior. In this study, we report a series of 13 cases of primary cutaneous epithelioid angiosarcoma and analyze their clinicopathologic features. The tumors arising in the conventional settings for cutaneous angiosarcoma (ie, in the head and neck region of elderly patients, and those occurring postradiation or associated with lymphedema) were excluded. Primary cutaneous epithelioid angiosarcoma occurred in adults (mean age, 66 y) with an equal sex distribution, and presented as solitary (n=10) or multiple (n=3) nodules ranging in size from 8 to 80 mm, with a predilection for the limbs (n=10). Histopathologically, the tumors comprised infiltrative sheets of atypical epithelioid cells within the dermis with or without the involvement of the subcutis. Vascular channel formation and intracytoplasmic lumina were seen, at least focally, in most cases. Mitoses were readily identified and necrosis was seen in 40% of the cases. The tumors were immunoreactive for vascular markers, with CD31 and FLI-1 offering the highest sensitivity. Pancytokeratin was positive in two thirds of the cases, and epithelial membrane antigen was positive in one-quarter of the cases. There was rare focal expression of Melan-A (n=2) and smooth muscle actin (n=3). Follow-up information was available for 11 patients. Six patients died of metastatic disease after a median follow-up of 12 months (range, 3 to 36 mo), and 1 patient died of unrelated causes. These findings suggest that primary cutaneous epithelioid angiosarcoma occurring outside the conventional settings of angiosarcoma is a highly aggressive malignant tumor with mortality rates in excess of 55% after 3 years.

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Year:  2011        PMID: 21164288     DOI: 10.1097/PAS.0b013e3181fee872

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


  5 in total

Review 1.  [Cutaneous angiosarcoma: new aspects].

Authors:  T Brenn
Journal:  Pathologe       Date:  2015-02       Impact factor: 1.011

2.  Epithelioid angiosarcoma: a clinicopathological study of 16 Chinese cases.

Authors:  Jingbo Wu; Xiaojing Li; Xiuping Liu
Journal:  Int J Clin Exp Pathol       Date:  2015-04-01

3.  Intimal sarcoma of the abdominal aorta and common iliac arteries presenting as epithelioid angiosarcoma of the skin: a case report.

Authors:  Shogo Tajima; Katsuyuki Hoshina; Tets Oushik; Kunihiro Shigematsu; Masashi Fukayama
Journal:  Int J Clin Exp Pathol       Date:  2015-05-01

Review 4.  Epithelioid Cutaneous Mesenchymal Neoplasms: A Practical Diagnostic Approach.

Authors:  Joon Hyuk Choi; Jae Y Ro
Journal:  Diagnostics (Basel)       Date:  2020-04-17

5.  Rapidly progressive and fatal case of extragenital cutaneous epithelioid angiosarcoma with visceral involvement.

Authors:  James Abbott; John Blake; Aaron M Secrest; Scott R Florell
Journal:  JAAD Case Rep       Date:  2019-12-24
  5 in total

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