| Literature DB >> 19854481 |
Hongbiao Jing1, Yanhong Tai, Dazhou Xu, Fan Yang, Ming Geng.
Abstract
Renal cell carcinomas (RCCs) associated with Xp11.2 translocations (Xp11.2 translocation RCCs) are rare and occur predominantly in children and adolescents. A case of such tumor in a 12-year boy is reported. Grossly the cut surface of the ill-defined mass was polychromatic, containing areas of hemorrhage and necrosis. Microscopically, the tumor was composed of epithelioid cells with clear to weakly eosinophilic cytoplasm arranged in nested, alveolar, and pseudopapillary formations. Immunohistochemically, the neoplastic cells were positive for transcription factor E3 and CD10. We concluded that this case was an Xp11.2 translocation RCC. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2009 PMID: 19854481 DOI: 10.1016/j.urology.2009.07.1276
Source DB: PubMed Journal: Urology ISSN: 0090-4295 Impact factor: 2.649