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Indian J Pathol Microbiol ; 2012 Oct-Dec 55(4): 569-571
Article in English | IMSEAR | ID: sea-145667

ABSTRACT

Ewing's sarcoma/primitive neuroectodermal tumor (ES/PNET) of the prostate is extremely rare. Here, we report a case of ES/PNET of prostate in a 24-year-old man presenting with dysuria and pelvic discomfort. Computed tomography scan revealed a heterogeneous mass involving the prostate without evidence of distant metastases. Histologically, the tumor was composed of small round blue cells strongly and diffusely positive for CD99 and epithelial markers. Fluorescence in situ hybridization confirmed rearrangement of the Ewing's sarcoma region on chromosome 22.


Subject(s)
Humans , Keratins/metabolism , Male , Neuroectodermal Tumors, Primitive, Peripheral/diagnosis , Neuroectodermal Tumors, Primitive, Peripheral/epidemiology , Neuroectodermal Tumors, Primitive, Peripheral/pathology , Prostate , Review Literature as Topic , Sarcoma, Ewing/diagnosis , Sarcoma, Ewing/epidemiology , Sarcoma, Ewing/pathology , Tomography, X-Ray Computed , Young Adult
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