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婴儿肥厚性幽门狭窄发病机制的新见解。

New insights into the pathogenesis of infantile pyloric stenosis.

作者信息

Panteli Christina

机构信息

Department of Paediatric Surgery, Norfolk and Norwich University Hospital, Colney Lane, Norwich NR4 7UY, UK.

出版信息

Pediatr Surg Int. 2009 Dec;25(12):1043-52. doi: 10.1007/s00383-009-2484-x. Epub 2009 Sep 16.

Abstract

Infantile hypertrophic pyloric stenosis (IHPS) is the most common surgical cause of vomiting in infants. Despite numerous hypotheses, the aetiopathogenesis of IHPS is not fully understood. Genetic, extrinsic and hormonal factors have been implicated in the pathogenesis of the disease. Furthermore, abnormalities of various components of the pyloric muscle such as smooth muscle cells, growth factors, extracellular matrix elements, nerve and ganglion cells, synapses, nerve supporting cells, neurotransmitters and interstitial cells of Cajal have been reported. Recently, genetic studies have identified susceptibility loci for IHPS and molecular studies have concluded that smooth muscle cells are not properly innervated in IHPS.

摘要

婴儿肥厚性幽门狭窄(IHPS)是婴儿呕吐最常见的外科病因。尽管有众多假说,但IHPS的病因发病机制尚未完全明确。遗传、外在和激素因素均与该病的发病机制有关。此外,已有报道称幽门肌的各种成分存在异常,如平滑肌细胞、生长因子、细胞外基质成分、神经和神经节细胞、突触、神经支持细胞、神经递质和 Cajal 间质细胞。最近,遗传学研究已确定了 IHPS 的易感基因座,分子研究得出结论,在 IHPS 中平滑肌细胞的神经支配不正常。

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