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肛门直肠畸形的产前诊断与新生儿管理——病例报告

Prenatal diagnosis and neonatal management of anorectal malformation--a case report.

作者信息

Calda P, Haslík L, Zizka Z, Brestt'ák M, Rygl M

机构信息

Charles University in Prague, First Faculty of Medicine, General Teaching Hospital, Department of Obstetrics and Gynaecology, Prague, Czech Republic.

出版信息

Prague Med Rep. 2009;110(3):255-60.

PMID:19655703
Abstract

Intestinal dilatation and hyperechogenic bowel, some typical ultrasonographic features of anorectal malformation, were found in the 21st week of a singleton pregnancy. These findings were associated with unilateral renal agenesis and a single umbilical artery. All prenatally diagnosed anomalies were confirmed postpartum. Development of the sonographic appearance of the anorectal malformation, prenatal and neonatal management are described and discussed.

摘要

在单胎妊娠的第21周,发现了肠道扩张和肠壁回声增强,这是肛门直肠畸形的一些典型超声特征。这些发现与单侧肾缺如和单脐动脉有关。所有产前诊断的异常在产后均得到证实。本文描述并讨论了肛门直肠畸形的超声表现演变、产前和新生儿管理。

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