Complete Diphallia With Associated Epispadias: A Rare Congenital Anomaly Diagnosed in Adulthood

Diphalia is an extremely rare urogenital condition presenting with penile duplication. Although it is typically diagnosed in the neonatal period due to associated congenital anomalies, some cases may present late without any related complications. Every case of diphallia presents a distinct set of symptoms and associations. In this case report, we underscore an interesting clinical presentation of diphallia in a 24-year-old male and the significance of individualized management of the condition.