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囊性纤维化与婴儿肥厚性幽门狭窄:二者有关联吗?

Cystic fibrosis and infantile hypertrophic pyloric stenosis: is there an association?

作者信息

Kakish Khalid S

机构信息

Department of Pediatrics, Jordan University of Science and Technology, Irbid, Jordan.

出版信息

Pediatr Pulmonol. 2002 May;33(5):404-5. doi: 10.1002/ppul.10089.

Abstract

Cystic fibrosis (CF) is the most common lethal genetic disease among Caucasian populations. The generally accepted incidence of CF in the United States is 1 in 3,200 in the Caucasian population. Intestinal obstructions and atresias have been described among patients with CF. An association of CF with infantile hypertrophic pyloric stenosis (IHPS) has not been previously documented. A review in our clinic of 72 patients with CF revealed IHPS in two. The incidence of 2.7% is greater than the 0.3% incidence expected in the general population. This ninefold increase in IHPS in patients with CF suggests an association between the two and warrants further investigation.

摘要

囊性纤维化(CF)是白种人群中最常见的致死性遗传病。在美国,白种人群中CF的普遍发病率为1/3200。CF患者中曾有肠梗阻和闭锁的描述。CF与婴儿肥厚性幽门狭窄(IHPS)之间的关联此前尚无文献记载。我们诊所对72例CF患者的回顾发现其中2例患有IHPS。2.7%的发病率高于普通人群预期的0.3%发病率。CF患者中IHPS发病率增加了9倍,提示两者之间存在关联,值得进一步研究。

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