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Diphallus with urethral duplications.

N Mutlu1, M Baykal, E Merder

  • 1Department of Medical Faculty, Kocaeli University, Istanbul, Turkey.

International Urology and Nephrology
|September 11, 1999
PubMed
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This case study details a rare congenital condition, diphallus with incomplete urethral duplication. Surgical intervention involved resecting the hypoplastic glans and anastomosing the urethras.

Area of Science:

  • Urology
  • Pediatric Surgery
  • Medical Case Reports

Background:

  • Diphallus, a rare congenital anomaly, involves complete duplication of the penis.
  • Urethral duplication can present with varying degrees of severity and associated anomalies.
  • Congenital anomalies of the genitourinary tract require careful diagnosis and management.

Observation:

  • A case of glandular diphallus with incomplete urethral duplication was observed.
  • Associated anomalies included a right kidney rotation anomaly and left complete ureteral duplication with an ectopic ureteral orifice.
  • The patient presented with a single bladder and good sphincter control.

Findings:

  • Surgical findings confirmed diphallus and incomplete urethral duplication.
  • The hypoplastic glans was resected during the operation.

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  • The urethral opening into the hypoplastic glans was anastomosed side-by-side with the other urethra.
  • Implications:

    • This case contributes to the understanding of rare genitourinary malformations.
    • Management strategies for diphallus and urethral duplication require individualized surgical planning.
    • Further literature review is necessary to fully comprehend the spectrum of diphallus and associated anomalies.