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首例患有无阴茎畸形和完全尿道闭锁的足月男性。

First Case of a Term Male Born with Aphallia and Complete Urethral Atresia.

机构信息

Medical College of Georgia, Augusta, GA.

Section of Urology, Department of Surgery, Medical College of Georgia-Augusta University, Augusta, GA.

出版信息

Urology. 2021 Oct;156:e127-e130. doi: 10.1016/j.urology.2021.05.038. Epub 2021 Jun 1.

Abstract

Aphallia is an exceedingly rare condition often associated with an array of genitourinary anomalies. Classically, aphallia was thought to have to co-exist with a urethral fistula for adequate urine outflow to avoid the sequelae of oligohydramnios, while the absence of a fistula has historically been incompatible with life. We report the first case of a prenatally unrecognized aphallia with complete urethral atresia in a full-term baby, without an associated fistula or ectopic urethra. We postulate a urachal cyst noted on prenatal ultrasound resolved into a patent urachus providing sufficient outflow to avoid sequelae of oligohydramnios and allowed for term birth.

摘要

无阴茎畸形是一种极为罕见的疾病,常伴有一系列泌尿生殖系统异常。经典理论认为,无阴茎畸形必须合并尿道瘘,以保证足够的尿液排出,从而避免羊水过少的后遗症,而没有瘘管则一直被认为是无法存活的。我们报告首例产前未识别的完全性尿道闭锁的无阴茎畸形足月新生儿,无瘘管或异位尿道。我们推测产前超声检查发现的脐尿管囊肿自行消退形成通畅的脐尿管,提供了足够的尿液流出,从而避免了羊水过少的后遗症,并允许足月分娩。

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