Megalourethra: A case report

Singh, Aditya; Ansari, Javed Salam; Shukla, Arvind Kumar; Farooq, Aadil; Chaturvedi, Veenita; Morya, DP

doi:10.5958/2319-5886.2014.00050.2

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2020

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“…Management of FMU is complex, because of lack of supportive corporal tissue. Moreover, associated life threatening anomalies often influence the management as well as the prognosis [10,11]. Additionally, sex reassignment or placement of penile prosthesis is often required in cases of FMU [12].…”

Section: Discussionmentioning

confidence: 99%

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Congenital megalourethra (CMU) is a dilatation of penile urethra without any distal obstruction. It occurs due to one or both corporal defect. About 80-100% cases of CMU are accompanied by multiple systems malformations which make the treatment more challenging. Cysto-urethrogram is necessary for radiological diagnosis and surgical planning. Depending on the type of the CMU and associated congenital anomalies, reduction urethroplasty or major reconstructive surgery is fashioned. We report a case of scaphoid variety of CMU in a 2 year child who was managed by reduction urethroplasty with additional dartos double breasting to prevent postoperative urethrocutaneous fistula (UCF).

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Megalourethra: A case report

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