|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|5688708||1409932||2017||3 صفحه PDF||ندارد||دانلود رایگان|
Primary renal Ewing sarcoma is extremely rare and carries a dismal prognosis. It is particularly diagnostically challenging due to its ability to mimic other round cell tumors. Herein we report such a case in a 28-year-old white female. The diagnosis was confirmed by immunophenotyping, fluorescence in situ hybridization, and reverse transcription polymerase chain reaction analyses.
Journal: Urology - Volume 99, January 2017, Pages e11-e13