Abstract
Paratesticular Rhabdomyosarcoma (RMS) is a rare tumor. Treatment must be multimodal and based on surgery, chemotherapy and radiotherapy. We report an observation of a paratesticular RMS in a child and willdiscuss the diagnostic and therapeuticmodalities in the highlight of a review of the literature.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have