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Published on: January 7, 2019
Scafoid megalourethra--a reliable surgical approach
Santiago Vallasciani1, Pietro Atzori, Luisa Martini
1Andrological and Gynecological Surgery Unit, Bambino Gesù Childrens Hospital, Rome, Italy.
Journal of Pediatric Surgery
|October 31, 2008
Summary
Congenital megalourethra, a rare condition with scaphoid and fusiform types, presents an unclear cause. A novel surgical technique successfully treated a boy with the scaphoid variant.
Area of Science:
- Urology
- Pediatric Surgery
- Medical Malformations
Background:
- Congenital megalourethra is an exceptionally rare congenital anomaly characterized by significant urethral dilation.
- It presents with two primary anatomical variants: scaphoid and fusiform.
- The precise etiology of congenital megalourethra remains incompletely understood and is a subject of ongoing research.
Observation:
- This report details a case of congenital megalourethra in a pediatric patient.
- The specific variant observed was the scaphoid type, presenting unique anatomical challenges.
- The patient's condition necessitated a specialized surgical intervention.
Findings:
- A novel surgical approach was developed and implemented for the treatment of scaphoid megalourethra.
- The surgical procedure was performed successfully on the affected boy.
- Post-operative outcomes indicate the efficacy of the proposed surgical method.
Implications:
- This case highlights a potentially effective surgical strategy for managing scaphoid congenital megalourethra.
- The findings may contribute to a better understanding of surgical interventions for rare urethral malformations.
- Further research and case studies are warranted to validate and refine this surgical approach for congenital megalourethra.

