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婴儿期孤立性回肠穿孔:先天性巨结肠的一种致命首发表现

Isolated Ileal Perforation in Infancy: A Lethal Initial Presentation of Hirschsprung's Disease.

作者信息

Iskandarani Fadi, Hammoud Chawki, Srour Sarah, Pelizzo Gloria, Nakib Ghassan, Calcaterra Valeria, Khanafer Amir

机构信息

Faculty of Medicine, Lebanese University, Hadath, Beirut, Lebanon.

Sahel General Hospital, Ghobeiri, Beirut, Lebanon.

出版信息

Pediatr Rep. 2017 Jun 26;9(2):7084. doi: 10.4081/pr.2017.7084.

Abstract

Arare case of ileal perforation, as a fatal initial presentation of total colonic aganglionosis (TCA) in infancy is reported. A 10-week-old boy, was brought to the emergency department with symptoms of complicated intestinal obstruction. He looked ill, was lethargic, markedly dehydrated and had a severely distended abdomen. An abdominal X-ray revealed multiple air fluid levels seen in a distended small intestine. During exploratory laparotomy the ileum was massively dilated with distal segment perforation. Ileal perforation repair was performed. A totally collapsed microcolon was identified. Biopsies were taken from the high rectum, sigmoid and hepatic flexure. Appendectomy and ileostomy were performed. All biopsies, as well as the appendix, showed absence of ganglion cells. Despite this procedure the patient progressively deteriorated and later died due to sepsis. Ileal perforation in infants is a rare, but potentially fatal initial presentation of TCA. Early detection is essential to prevent life-threatening complications.

摘要

本文报告了一例罕见的回肠穿孔病例,这是婴儿期全结肠无神经节症(TCA)的致命首发表现。一名10周大的男孩因复杂肠梗阻症状被送往急诊科。他看起来病恹恹的,嗜睡,明显脱水,腹部严重膨胀。腹部X光显示扩张的小肠内有多个气液平面。在剖腹探查术中,回肠大量扩张,远端肠段穿孔。进行了回肠穿孔修复术。发现一个完全塌陷的小结肠。从高位直肠、乙状结肠和肝曲取了活检组织。进行了阑尾切除术和回肠造口术。所有活检组织以及阑尾均显示无神经节细胞。尽管进行了该手术,患者病情仍逐渐恶化,后来因败血症死亡。婴儿回肠穿孔是TCA一种罕见但可能致命的首发表现。早期检测对于预防危及生命的并发症至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdc6/5494443/21a87221dbb9/pr-9-2-7084-g001.jpg

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