Male adult with incomplete urethral duplication: A case report from Indonesia

Abstract

Urethral duplication is a rare disease with diverse clinical symptoms and more common in male; only fewer than 300 instances have been reported. In this case report, a 20-year-old male patient came to the urology polyclinic with two holes on the glans penis, accompanied by daily clear discharge in the upper hole. This complaint has been experienced since birth. The patient underwent an excision of the dorsal accessory urethra to correct penile anomalies.

Keywords

• Urethral duplication
• Congenital disease
• Effman's classification
• Congenital anomalies