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儿童先天性巨结肠症

Hirschsprung's disease in children.

作者信息

Teitelbaum D H

机构信息

University of Michigan Hospital, Ann Arbor, USA.

出版信息

Curr Opin Pediatr. 1995 Jun;7(3):316-22. doi: 10.1097/00008480-199506000-00014.

Abstract

Several advances in understanding Hirschsprung's disease have developed in the past year. A greater understanding of the etiology of the disease has developed through the association of Hirschsprung's disease with a lack of neural cell adhesion molecule expression and nitric oxide in aganglionic portions of the bowel. It appears that a loss of neural cell adhesion molecule could be the cause of neurocytes failing to migrate to aganglionic regions, and a loss of nitric oxide could well explain the spasticity associated with the aganglionic region. Another advance has come from the analysis of genetic deletions associated with some forms of Hirschsprung's disease. Surgical advances have primarily been related to the increased use of a primary pull-through procedure in the newborn period. Results of this application have led to excellent outcomes without the need for a decompressive colostomy.

摘要

在过去一年里,人们对先天性巨结肠病的认识有了多项进展。通过将先天性巨结肠病与肠道无神经节段中神经细胞黏附分子表达缺失及一氧化氮缺乏联系起来,对该病病因有了更深入的了解。似乎神经细胞黏附分子的缺失可能是神经细胞无法迁移至无神经节区域的原因,而一氧化氮的缺乏很可能解释了与无神经节区域相关的痉挛。另一项进展来自对与某些形式的先天性巨结肠病相关的基因缺失的分析。手术方面的进展主要与新生儿期一期拖出术的使用增加有关。这种应用的结果带来了极佳的效果,无需进行减压结肠造口术。

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