先天性前尿道瘘伴持续性尿道沟。

Pub Date : 2021-01-01 Epub Date: 2021-01-29 DOI:10.1055/s-0040-1721469
Hazem Mosa, Massimo Garriboli
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引用次数: 1

摘要

摘要先天性前尿道瘘(CAUF)是一种罕见的阴茎异常,文献中仅报道了63例。这种异常可以单独出现,也可以与脊索或尿道下裂合并出现。我们报告一例8个月大的男孩CAUF类似于胚胎尿道沟。检查发现,宽尿道沟覆盖阴茎中轴,形成良好的尿道向近端和远端延伸,腺体解剖正常,腺道宽,包皮完整。尿道沟呈管状,呈层状覆盖。手术并发早期浅表皮肤开裂,但不影响尿道修复。然后进行皮肤重塑。在7年的随访中,观察到令人满意的美学和功能结果。明确CAUF和远端尿道的解剖结构是治疗这些儿童的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Congenital Anterior Urethrocutaneous Fistula with a Persistent Urethral Groove.

Congenital Anterior Urethrocutaneous Fistula with a Persistent Urethral Groove.

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Congenital Anterior Urethrocutaneous Fistula with a Persistent Urethral Groove.

Congenital anterior urethrocutaneous fistula (CAUF) is a rare penile anomaly with only 63 cases reported in the literature. The anomaly can present in isolation or in association with chordee or hypospadias. We report the case of an 8-month-old boy with CAUF that resembles the embryological urethral groove. On examination, a wide urethral groove was noted to cover the midshaft of the penis with a well formed urethra extending proximally and distally and with a normal glandular anatomy, a wide glandular meatus, and a complete foreskin. The urethral groove was tubularized and covered in layers. Surgery was complicated with early superficial skin dehiscence not affecting the urethral repair. Refashioning of the skin was then performed. A satisfactory aesthetic and functional outcome was observed at 7 years' follow-up. Defining the anatomy of CAUF and distal urethra is key in management of these children.

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