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Published on: June 16, 2022
[Incomplete urethral duplication in a male. A case report]
D Muñoz Vélez1, V Riera Marí, M Ozonas Moragues
1Servicio de Urología, Hospital Universitario Son Dureta, Palma de Mallorca.
Actas Urologicas Espanolas
|March 25, 2005
Summary
This case report details a rare instance of urethral duplication in a 20-year-old male, diagnosed via imaging. The condition, characterized by a double urethral meatus, required no intervention after ruling out other anomalies.
Area of Science:
- Urology
- Congenital Anomalies
- Medical Imaging
Background:
- Urethral duplication is a rare congenital anomaly primarily affecting males.
- Diagnosis typically occurs during pediatric age, making adult presentation unusual.
Observation:
- A 20-year-old male presented with a double urethral meatus and a double urinary stream.
- Physical examination revealed an additional hypospadic meatus inferior to a normally positioned meatus.
Findings:
- Retrograde urethro-cystography and voiding cysto-urethrograms confirmed two distinct urethras originating from a common bladder neck.
- The patient was diagnosed with Effmann type IIA2 incomplete urethral duplication.
Implications:
- This case highlights the possibility of late diagnosis for urethral duplication.
- Management should involve thorough investigation for associated anomalies.
- Conservative management may be appropriate in the absence of complications or other anomalies.
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