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Complete duplication of the penis - A case report
Saidanvar Agzamkhodjayev1,2, Kobiljon Ergashev1, Zafar Abdullayev1,2
1Department of Urology, National Children's Medical Center, Tashkent, Uzbekistan.
Urology Case Reports
|November 8, 2021
Summary
Penile duplication is a rare congenital condition. This case details a complete true duplication treated with side-to-side urethra-urethral anastomosis, preserving the posterior urethra to prevent incontinence.
Area of Science:
- Urology
- Pediatric Surgery
- Congenital Anomalies
Background:
- Penile duplication (diphallia) is an extremely rare congenital anomaly.
- It can present with various associated urogenital, gastrointestinal, and musculoskeletal abnormalities.
- Accurate classification is crucial for determining appropriate surgical management.
Observation:
- The study presents a case of complete true penile duplication.
- The patient underwent a surgical procedure involving side-to-side urethra-urethral anastomosis.
- Care was taken to preserve the posterior urethra during the procedure.
Findings:
- Successful surgical management of complete true penile duplication was achieved.
- Preservation of the posterior urethra was a key surgical consideration.
- The chosen surgical technique aimed to minimize the risk of postoperative urinary incontinence.
Implications:
- This case highlights a successful surgical approach for complete true penile duplication.
- Preserving the posterior urethra is vital for maintaining urinary continence postoperatively.
- Effective classification and tailored surgical strategies are essential for managing this rare congenital condition.