Cytological diagnosis of angiosarcoma arising in an immunosuppressed patient 6 years after multi‐visceral transplantation. Issue 10 (7th November 2013)

• Record Type: Journal Article
• Authors: Chen, Xiaowei; Lagana, Stephen M.; Poneros, John; Kato, Tomoaki; Remotti, Fabrizio; He, Huangjun; Kaminsky, Dmitry; Hamele‐Bena, Diane
• Is Part Of: Diagnostic cytopathology. Volume 42:Issue 10(2014:Oct.)
• Page Start: 884
• Page End: 889
• Publication Date: 2013-11-07
• Subjects: Cytodiagnosis -- Periodicals; Pathology, Cellular -- Periodicals; Cytology -- Periodicals; 616.07582
• DOI: 10.1002/dc.23068
• Languages: English
• ISSNs: 8755-1039

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Angiosarcoma is a rare and aggressive malignant tumor of soft tissue. It can arise in almost any part of the body, most commonly in the skin and the superficial soft tissue in the head and neck region. Although the etiology of angiosarcoma is unknown, there are several well‐known risk factors, such as chronic lymphedema, exposure to radiation, toxins, and foreign bodies. It rarely occurs in transplant patients. Cytological criteria for the diagnosis of angiosarcoma have not been fully established, having been described only in a few cases, mostly fine‐needle aspiration biopsies (FNAB). Herein, we present a case of angiosarcoma arising in an immunosuppressed patient status post multi‐visceral transplantation and diagnosed by cytology. To the best of our knowledge, this is the first report of such a case in the English literature. The cytological findings from endoscopic ultrasound‐guided FNAB and ascites fluid are discussed. Diagn. Cytopathol. 2014;42:884–889. © 2013 Wiley Periodicals, Inc.</p> </abstract>