Distal Urethral Duplication in a Female Child: A Unique Case Report with Diverticular Component

Gokhan Arkan1, Cem Kaya1, Leyla Nur Turker1

  • 1Department of Pediatric Surgery, Gazi University Faculty of Medicine, Ankara, Turkey.

Insights

Urethral duplication (UD) is a rare condition in girls presenting with urinary incontinence. Surgical excision of the duplicated tract effectively treated a pediatric case, resolving symptoms and showing no recurrence.

Area of Science:

  • Pediatric Urology
  • Congenital Anomalies
  • Surgical Case Report

Background:

  • Urethral duplication (UD) is an exceptionally rare congenital anomaly in females.
  • It can manifest with symptoms such as urinary incontinence and clitoral swelling.
  • Early diagnosis and intervention are crucial for optimal outcomes.

Observation:

  • A 5-year-9-month-old girl presented with postvoid dribbling and clitoral swelling.
  • Imaging and physical examination identified a fistula tract.
  • Surgical exploration revealed a urethral duplication extending from the distal urethra to the clitoris.

Findings:

  • The identified fistula tract, representing urethral duplication, was successfully dissected and excised.
  • Post-operative recovery was uneventful, with complete resolution of clitoral swelling and urinary dribbling.
  • No recurrence was observed at the 2-month follow-up, indicating successful surgical management.

Implications:

  • This case highlights the importance of considering urethral duplication in the differential diagnosis of urinary incontinence in pediatric females.
  • Surgical excision of the duplicated urethral tract is an effective treatment modality.
  • Favorable outcomes and symptom resolution can be achieved with timely surgical intervention.
Abstract

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