Abstract
Fetal rhabdomyoma (F-RM) is a very rare tumor that usually occurs in the head and neck. Paratesticular F-RM in children is extremely rare. In this article, we report the case of a 12-year-old boy diagnosed with paratesticular F-RM. The patient was well, with no local recurrence or metastasis 5 years after excision of the tumor. To our knowledge, this is the first case of F-RM reported in an adolescent. We also reviewed the literature and compared our patient with the 11 previously reported patients with F-RM.
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