Abstract

Paratesticular rhabdomyosarcoma is a rare and highly aggressive tumor that primarily affects the urogenital system. Despite being relatively uncommon, this disease presents significant challenges due to its aggressive nature. The embryonal subtype is the most frequently encountered. Treatment often requires a multimodality approach, combining surgery, chemotherapy, and radiation therapy, to improve patient outcomes. We report an observation of a paratesticular rhabdomyosarcoma in a 16-year-old patient. We discuss diagnostic and therapeutic modalities based on data from the literature.