阴茎发育不全合并波特序列征。

Penile agenesis complicated by Potter sequence.

作者信息

Arai M, Suzuki S, Ishino H, Igarashi K, Araki T

机构信息

Department of Obstetrics and Gynecology, Nippon Medical School, Tokyo, Japan.

出版信息

Arch Gynecol Obstet. 2001 Nov;265(4):219-20. doi: 10.1007/s004040000162.

DOI:10.1007/s004040000162

PMID:11789751

Abstract

We present a case of penile agenesis complicated by multicystic dysplastic kidneys and urethral agenesis, which resulted in oligohydramnios, pulmonary hypoplasia and neonatal death. In this case, no external urethral opening was found, and the gastrointestinal tract showed no anomaly. Cases of penile agenesis complicated by Potter sequence with urethral agenesis should be differentiated from those with ectopic urethral openning.

摘要

我们报告一例阴茎发育不全合并多囊性发育不良肾和尿道闭锁的病例，该病例导致羊水过少、肺发育不全及新生儿死亡。在此病例中，未发现尿道外口，且胃肠道无异常。阴茎发育不全合并波特序列征及尿道闭锁的病例应与尿道异位开口的病例相鉴别。