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先天性巨结肠症中的肠穿孔

Bowel perforation in Hirschsprung's disease.

作者信息

Newman B, Nussbaum A, Kirkpatrick J A

出版信息

AJR Am J Roentgenol. 1987 Jun;148(6):1195-7. doi: 10.2214/ajr.148.6.1195.

Abstract

A review of the medical records of 45 infants less than 1 year old with Hirschsprung's disease identified two (4.4%) who presented with bowel perforation. A literature survey was done to evaluate the relationship between bowel perforation of the bowel early in the course of Hirschsprung's disease indicates that: the infant under 4 months old is at the greatest risk; the majority of cases (62%) were associated with long-segment or total colonic Hirschsprung's disease; the most common sites of perforation were the proximal colon (68%) and appendix (17%); in cases with a short or intermediate length of aganglionic bowel, the perforation was proximal to or at the site of transition, but in 84% of infants with total colonic aganglionosis the perforation was situated in aganglionic bowel. Hirschsprung's disease should be a prime differential consideration in a young infant with penumoperitoneum caused by distal bowel perforation.

摘要

对45例1岁以下患先天性巨结肠症婴儿的病历回顾发现,有2例(4.4%)出现肠穿孔。进行了一项文献调查以评估先天性巨结肠症病程早期肠穿孔之间的关系,结果表明:4个月以下婴儿风险最高;大多数病例(62%)与长段或全结肠先天性巨结肠症相关;最常见的穿孔部位是近端结肠(68%)和阑尾(17%);在无神经节肠段短或中等长度的病例中,穿孔位于过渡段近端或该部位,但在84%的全结肠无神经节细胞症婴儿中,穿孔位于无神经节肠段。对于因远端肠穿孔导致气腹的幼儿,先天性巨结肠症应作为主要的鉴别诊断考虑。

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