Paratesticular Pleomorphic Rhabdomyosarcoma: A Report of Two Cases
Author(s) -
R. Boulma,
M Gargouri,
Ahmed Sallemi,
Mohamed Chlif,
Zouhaier Fitouri,
Yosri Kallel,
Yassine Nouira
Publication year - 2013
Publication title -
case reports in urology
Language(s) - English
Resource type - Journals
eISSN - 2090-696X
pISSN - 2090-6978
DOI - 10.1155/2013/807979
Subject(s) - medicine , orchiectomy , rhabdomyosarcoma , adjuvant chemotherapy , immunohistochemistry , pathology , embryonal rhabdomyosarcoma , surgery , sarcoma , cancer , breast cancer
Pleomorphic rhabdomyosarcoma (RMS) is a rare tumor with an aggressive behavior, described mainly in adulthood. Herein we present two cases of paratesticular pleomorphic RMS in 71- and 16-year-old patients with metastases at initial diagnosis. Histological, immunohistochemical, and ultrastructural findings were essential to confirm diagnosis. Few months after radical orchiectomy, both patients died before or just after starting adjuvant chemotherapy.
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