subtypes, alveolar rhabdomyosarcoma and embryonal rhabdomyosarcoma, constitute 20
and 60% of all cases, respectively. Approximately 80% of alveolar rhabdomyosarcoma carry
two signature chromosomal translocations, t (2; 13)(q35; q14) resulting in PAX3–FOXO1
fusion, and t (1; 13)(p36; q14) resulting in PAX7–FOXO1 fusion. Whether the remaining
cases are truly negative for gene fusion has been questioned. We are reporting the case of a …