Duplication of the glans penis manifested at puberty

Area of Science:

• Urology
• Pediatric Surgery
• Congenital Malformations

Background:

• Congenital anomalies of the external genitalia are rare.
• Complete duplication of the glans penis is an exceptionally rare malformation.
• This case highlights a unique presentation of glans duplication.

Observation:

• A patient presented with complete glans penis duplication, prepuce, and a blind-ending urethra.
• The malformation was not detected in infancy or childhood.
• Symptoms manifested during puberty due to external genitalia growth.

Findings:

• The glans duplication was an isolated finding, not associated with other urinary tract malformations.
• Surgical excision of the duplicated glans was performed.
• The surgical procedure was uncomplicated and yielded a positive outcome.

Implications:

• This case expands the understanding of rare penile congenital anomalies.
• Early recognition and surgical intervention can lead to favorable outcomes.
• Further research into the embryological basis of such duplications may be warranted.