Abstract
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.