Glandular diphallus with urethral duplication: Conventional technique for a rare congenital anomaly

腺体性双阴茎伴尿道重复畸形:一种罕见先天性畸形的常规治疗方法

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Abstract

Diphallus is a rare anomaly and its association with urethral duplication is extremely rare. Numerous associated genitourinary and gastrointestinal anomalies have been reported with this condition. Challenges in the management are incorporation of the glans and the dominant urethra during reconstruction. We report the successful management of a case of glandular diphallus with complete urethral duplication retaining the dorsal urethra.

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