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Urethral duplication: case report and literature review
Hussaini Y Maitama1, Hycinth N Mbibu, Usman M Tella
1Department of Surgery, Urology Division, Ahmadu Bello University Teaching Hospital, Shika, Zaria, Nigeria.
Urethral duplication is a rare congenital condition causing double urinary streams. Early diagnosis and surgical repair lead to good outcomes, highlighting the need for careful evaluation after circumcision.
Area of Science:
- Pediatric Urology
- Congenital Abnormalities
- Genitourinary Surgery
Background:
- Urethral duplication is an uncommon congenital anomaly of the genitourinary system.
- Literature on urethral duplication is limited, necessitating case reports to expand understanding.
- This report emphasizes the importance of a high index of suspicion for diagnosis.
Observation:
- A six-year-old male presented with urinary passage from two penile orifices post-circumcision.
- The patient exhibited double urinary streams: one clear, one with hematuria.
- Physical examination revealed a normal urethral meatus and an accessory dorsal opening.
Findings:
- Diagnosis of urethral duplication requires thorough evaluation and a high index of suspicion.
- Surgical management, including single-stage urethroplasty, resulted in a favorable outcome.
- Understanding the specific duplication anatomy is crucial for surgeons to prevent complications.
Implications:
- This case contributes to the limited literature on urethral duplication.
- Highlights the potential for iatrogenic injury or misdiagnosis following procedures like circumcision.
- Underscores the importance of skilled surgical intervention for optimal patient outcomes.
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