Abstract

Rhabdomyosarcoma is one of the most frequent soft tissue sarcomas in children. It is found mostly in children, primarily infants, toddlers, and pre-school pupils. However, pure testicular rhabdomyosarcoma is a very rare tumor and few cases have been reported in literature. The tumor usually presents as a painless testicular enlargement with early dissemination via the blood stream and lymphatics. The origin of this tumor is presumed to be from overgrowth of a sarcomatous area of the teratoma. Here, we present a case of testicular rhabdomyosarcoma in a 15-year-old student with a fatal outcome during chemotherapy. This is actually the first case of pure testicular rhabdomyosarcoma diagnosed in this centre after over 10 years.   

Key words: Rhabdomyosarcoma, testicular, orchidectomy, chemotherapy.