Wang Hong-Liang, Liu Ling-Yun, Tian Run-Hui, Li Fu-Biao, Guo Kai-Min
Department of Andrology, Norman Bethune First Hospital, Jilin University, Changchun, Jilin 130021, P.R. China.
Department of Psychology, Norman Bethune First Hospital, Jilin University, Changchun, Jilin 130021, P.R. China.
Mol Clin Oncol. 2016 Apr;4(4):625-627. doi: 10.3892/mco.2016.733. Epub 2016 Jan 18.
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.
睾丸旁横纹肌肉瘤(RMS)在成人中是一种极其罕见的恶性肿瘤,占所有RMS病例的7%,占所有非生殖细胞性阴囊内肿瘤的6%。其临床症状与鞘膜积液或睾丸肿瘤相似,通常表现为腹股沟管或阴囊内的单侧无痛性肿块。目前尚无针对该肿瘤的特异性血清标志物。附睾RMS极为罕见。特别是当它与附睾炎相关时,这种恶性肿瘤通常会被忽视。我们在此报告一例附睾胚胎性RMS病例,表现为阴囊疼痛性水肿,被误诊为附睾炎。该患者术后接受了3个周期的辅助化疗,随访4年后无疾病复发。