一例复杂的高位泄殖腔畸形：病例报告

A complex, high cloacal malformation: case report.

作者信息

Wagner G, Holschneider A M, Gharib M

机构信息

Department of Pediatric Surgery, Kinderkrankenhaus der Stadt Köln, Cologne, Germany.

出版信息

Eur J Pediatr Surg. 1998 Jun;8(3):182-5. doi: 10.1055/s-2008-1071150.

DOI:10.1055/s-2008-1071150

PMID:9676404

Abstract

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 exstrophic bladder plate. Additional anomalies included an omphalocele and malformations of the upper urinary tract and the lower extremities, skeleton, and vertebral column.

摘要

泄殖腔畸形是早期胚胎发育罕见、复杂的抑制性异常。我们报告一名患有泄殖腔畸形的患者，其纵隔阴道和直肠瘘通过一个共同开口排入膀胱外翻板。其他异常包括脐膨出以及上尿路、下肢、骨骼和脊柱的畸形。