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Diphallus with urethral duplication: a rare case

N Mutlu1, M Baykal, E Merder

  • 1Medical Faculty, Kocaeli University, Turkey.

International Journal of Clinical Practice
|April 16, 1998
PubMed
Summary
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This case study details diphallus with incomplete urethral duplication and associated kidney anomalies. Surgical intervention involved resecting the hypoplastic glans and anastomosing the urethra.

Area of Science:

  • Urology
  • Pediatric Surgery
  • Medical Case Reports

Background:

  • Diphallus, a rare congenital anomaly, involves complete duplication of the penis.
  • Urethral duplication can occur with diphallus, presenting complex surgical challenges.
  • Associated renal anomalies, such as rotation and duplication anomalies, are frequently observed.

Observation:

  • A patient presented with glandular diphallus and incomplete urethral duplication.
  • The condition was associated with a right kidney rotation anomaly.
  • The left kidney exhibited a bifid pelvis and an ectopic ureteral orifice.

Findings:

  • The bladder was single with preserved sphincter control.
  • Surgical management included resection of the hypoplastic glans.

Related Experiment Videos

  • The urethra opening into the hypoplastic glans was anastomosed alongside the other urethra.

    • Implications:

    • This case highlights the complex anatomical variations associated with diphallus and urethral duplication.
    • Understanding these associations is crucial for effective surgical planning and patient management.
    • Further discussion on diphallus and incomplete urethral duplication is warranted to improve clinical outcomes.