A complex, high cloacal malformation: Case report

被引：2
|
作者：
Wagner, G [1 ]
Holschneider, AM [1 ]
Gharib, M [1 ]
机构：
[1] Kinderkrankenhauses Stadt Koln, Kinderchirurg Klin, Dept Pediat Surg, D-50735 Koln, Germany
来源：
EUROPEAN JOURNAL OF PEDIATRIC SURGERY | 1998年 / 8卷 / 03期
关键词：
cloacal malformation; vesicointestinal fissure; bladder exstrophy; anal agenesis; rectovaginal fistula; omphalocele; absent external genitalia; urogenital sinus;
D O I：
10.1055/s-2008-1071150
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Cloacal malformations are rare, complex inhibitional anomalies of early embryogenesis. We report a patient with a cloacal malformation in which a septate vagina and a rectal fistula emptied through a common orifice onto an ex-strophic bladder plate. Additional anomalies included an omphalocele and malformations of the upper urinary tract and the lower extremities, skeleton, and vertebral column.
引用
收藏
页码：182 / 185
页数：4
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