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一名自闭症儿童因原发性小肠毛粪石和梅克尔憩室导致回肠套叠的罕见病例。

A Rare Case of Ileal Intussusception Caused by Primary Small Bowel Trichobezoar and Meckel's Diverticulum in an Autistic Child.

作者信息

Messaoud Marwa, Joya Habib Ullah, Alansari Amani N, Jouini Abir, Ksiaa Amine, Zrig Ahmed, Sahnoun Lasaad

机构信息

Pediatric Surgery Department, Fattouma Bourguiba Hospital University of Monastir Monastir Tunisia.

Department of Pediatric Surgery Hamad Medical Cooperation Doha Qatar.

出版信息

Clin Case Rep. 2025 Aug 4;13(8):e70745. doi: 10.1002/ccr3.70745. eCollection 2025 Aug.

Abstract

Intussusception is a condition in which one part of the intestine slides into an adjacent part of the intestine. Intussusception is an important cause of an acute abdomen and the second most common cause of bowel obstruction in children. Trichobezoars, which are rare in children and often linked to psychiatric disorders, seldom cause intestinal intussusception. While Rapunzel syndrome-a form of gastric trichobezoar extending into the small bowel-is a recognized cause, primary small-bowel trichobezoars are exceptionally rare. We report a unique pediatric case of ileo-ileal intussusception triggered by a 30-cm primary small-bowel trichobezoar coexisting with Meckel's diverticulum, an association not previously documented. A 6-year-old autistic boy presented with symptoms suggestive of bowel obstruction. Imaging suggested small-bowel intussusception related to Meckel's diverticulum. Surgery revealed an ileo-ileal intussusception secondary to a 30-cm obstructive trichobezoar located proximal to the invagination and an inflamed Meckel's diverticulum. The diverticulum was resected, the trichobezoar was removed, and ileo-ileal anastomosis was performed, with no postoperative complications. The combination of a primary small-bowel trichobezoar and Meckel's diverticulum leading to intussusception is exceedingly rare and poses unique diagnostic and therapeutic challenges, particularly in special pediatric populations. Early recognition and surgical intervention are essential to prevent bowel ischemia, perforation, and sepsis.

摘要

肠套叠是一段肠管滑入相邻肠管的一种病症。肠套叠是急腹症的一个重要病因,也是儿童肠梗阻的第二大常见病因。毛粪石在儿童中罕见,且常与精神疾病相关,很少引起肠套叠。虽然拉普索恩综合征(一种延伸至小肠的胃毛粪石形式)是一种公认的病因,但原发性小肠毛粪石极为罕见。我们报告了一例独特的儿科病例,一名6岁的自闭症男孩出现肠梗阻症状。影像学检查提示小肠套叠与梅克尔憩室有关。手术发现回肠-回肠套叠继发于一个位于套叠近端的30厘米阻塞性毛粪石和一个发炎的梅克尔憩室。切除憩室,取出毛粪石,并进行回肠-回肠吻合术,术后无并发症。原发性小肠毛粪石与梅克尔憩室合并导致肠套叠极为罕见,带来了独特的诊断和治疗挑战,尤其是在特殊儿科人群中。早期识别和手术干预对于预防肠缺血、穿孔和败血症至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a152/12321601/8070fd4b332f/CCR3-13-e70745-g001.jpg

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