Guennouni Asmae, Abourak Chaimae, Bahha Soukaina, Esseti Sarra, El Haddad Siham, Allali Nazik, Chat Latifa, Sassi Samia, Lamalmi Najat
Centre Hospitalier Ibn Sina, Rabat, Morocco.
Sage Open Pediatr. 2025 Jul 10;12:30502225251346270. doi: 10.1177/30502225251346270. eCollection 2025 Jan-Dec.
Paratesticular rhabdomyosarcoma (RMS) is a rare tumor. Imaging helps diagnose the tumor process, while histopathological examination with immunohistochemistry confirms the diagnosis. Treatment should be multimodal, involving surgery, chemotherapy, and radiotherapy. In light of this observation and a review of the literature, discuss a case of paratesticular rhabdomyosarcoma with invasion of the ipsilateral testicle.
睾丸旁横纹肌肉瘤（RMS）是一种罕见的肿瘤。影像学有助于诊断肿瘤进程，而免疫组化的组织病理学检查可确诊。治疗应采用多模式，包括手术、化疗和放疗。鉴于这一观察结果并回顾文献，讨论一例侵犯同侧睾丸的睾丸旁横纹肌肉瘤病例。
