Paratesticular rhabdomyoma

Eric A. Kurzrock; J. Erik Busby; Regina Gandour-Edwards

doi:10.1016/S0022-3468(03)00513-X

Paratesticular rhabdomyoma

Eric A. Kurzrock, J. Erik Busby, Regina Gandour-Edwards

Research output: Contribution to journal › Article

11 Scopus citations

Abstract

A case of rhabdomyoma of the spermatic cord in an infant with cryptorchidism is reported. This extremely rare tumor has not been described in an extrascrotal position or at such a young age. Differential diagnosis includes malignant rhabdomyosarcoma. Although fetal-type rhabdomyoma of the head and neck generally is a benign tumor, the prognosis of paratesticular fetal-type rhabdomyoma is unknown. Long-term follow-up is recommended.

Original language	English (US)
Pages (from-to)	1546-1547
Number of pages	2
Journal	Journal of Pediatric Surgery
Volume	38
Issue number	10
DOIs	https://doi.org/10.1016/S0022-3468(03)00513-X
State	Published - Oct 1 2003

Keywords

Genitalia
Infant
Male
Rhabdomyoma
Spermatic cord

ASJC Scopus subject areas

Surgery

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10.1016/S0022-3468(03)00513-X

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Kurzrock, E. A., Busby, J. E., & Gandour-Edwards, R. (2003). Paratesticular rhabdomyoma. Journal of Pediatric Surgery, 38(10), 1546-1547. https://doi.org/10.1016/S0022-3468(03)00513-X

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AB - A case of rhabdomyoma of the spermatic cord in an infant with cryptorchidism is reported. This extremely rare tumor has not been described in an extrascrotal position or at such a young age. Differential diagnosis includes malignant rhabdomyosarcoma. Although fetal-type rhabdomyoma of the head and neck generally is a benign tumor, the prognosis of paratesticular fetal-type rhabdomyoma is unknown. Long-term follow-up is recommended.

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