| Literature DB >> 27073679 |
Hong-Liang Wang1, Ling-Yun Liu1, Run-Hui Tian2, Fu-Biao Li1, Kai-Min Guo1.
Abstract
Paratesticular rhabdomyosarcoma (RMS) is an extremely rare malignancy in adults, accounting for 7% of all RMS cases and 6% of all non-germinal intrascrotal tumors. The clinical signs are similar to those of a hydrocele or testicular tumor, typically presenting as a unilateral, painless mass in the inguinal canal or scrotum. No specific serum markers are currently available for this tumor. RMS of the epididymis is extremely rare. Particularly when it is associated with epididymitis, this malignancy is usually overlooked. We herein present a case of epididymal embryonal RMS, manifesting an painful scrotal edema, misdiagnosed as epididymitis. The patient received 3 cycles of adjuvant chemotherapy postoperatively and remained disease-free after 4 years of follow-up.Entities:
Keywords: embryonal rhabdomyosarcoma; epididymis; epididymitis
Year: 2016 PMID: 27073679 PMCID: PMC4812556 DOI: 10.3892/mco.2016.733
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450