Infant with recurrent ventriculoperitoneal shunt migration to right scrotum

Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
Amanda Paterson, Richard Ferch

Abstract

Migration of the distal catheter of a ventriculoperitoneal shunt to the scrotum is a documented but rare event. We present a case in which a 13 month old infant with hydrocephalus had recurrent migration of the peritoneal catheter to the right scrotum associated with a developing hydrocele. The patient underwent two revision operations and the distal catheter was ultimately shortened. He later underwent bilateral inguinal hernia repairs.

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