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Squamous cell carcinoma with rhabdoid phenotype of skin/soft tissue in a transplant patient: An exceptional case and review of the literature

Identifieur interne : 003A43 ( Main/Exploration ); précédent : 003A42; suivant : 003A44

Squamous cell carcinoma with rhabdoid phenotype of skin/soft tissue in a transplant patient: An exceptional case and review of the literature

Auteurs : Pushpa Allam-Nandyala [États-Unis] ; Marilyn M. Bui [États-Unis] ; Ronald Deconti [États-Unis] ; Chetna Purohit [États-Unis] ; Soner Altiok [États-Unis]

Source :

RBID : ISTEX:7AF021AECF3C82BAEB84E649519738F863C90683

Abstract

Squamous cell carcinoma with rhabdoid features (SCCRF) is a very rare and unusual cutaneous tumor. Here, we report an extraordinary case diagnosed by fine needle aspiration biopsy, in a 66‐year‐old man, status post multiple organ transplantation. The patient presented with a large ulcerating fungating mass in his forearm that had all the light microscopic and immunohistochemical features of a SCCRF. Previously six cases of SCCRF phenotype diagnosed by surgical pathology have been reported. This is the first case diagnosed cytologically. A review of the literature with emphasis on the differential diagnoses of such unusual rhabdoid‐like tumors in fine‐needle aspiration biopsy and the potential molecular mechanism for rhabdoid phenotype in transplant patients are discussed. Diagn. Cytopathol. 2013. © 2011 Wiley Periodicals, Inc

Url:
DOI: 10.1002/dc.21788


Affiliations:


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