直肠闭锁、后鼻孔闭锁与先天性心脏病：一种罕见的关联。
Rectal atresia, choanal atresia and congenital heart disease: a rare association.
作者信息
Saxena A K, Morcate J J, Schleef J, Reich A, Willital G H
机构信息
Pediatric Surgical University Clinic, Münster D-48129, Germany.
出版信息
Technol Health Care. 2004;12(4):343-5.
PMID:15502285
Abstract
Rectal atresia is an extremely rare anorectal malformation. A unique case of rectal atresia presenting as an imperforate membrane associated with congenital cardiac malformations and unilateral choanal atresia in a newborn is reported. Ultrasound examination in the newborn infant located the presence of the rectal membrane which was surgically treated successfully.
摘要
直肠闭锁是一种极其罕见的肛肠畸形。本文报道了一例独特的直肠闭锁病例，该病例表现为一名新生儿的无孔隔膜，伴有先天性心脏畸形和单侧后鼻孔闭锁。对该新生儿进行超声检查发现了直肠隔膜的存在，并成功进行了手术治疗。
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