Intestinal intussusception from a Meckel's diverticulum and intestinal malrotation: a case report

IF 0.2 Q4 PEDIATRICS
Rawan Sharma, Shin Miyata, Olivia Gentry, Christopher Blewett, Richard Herman
{"title":"Intestinal intussusception from a Meckel's diverticulum and intestinal malrotation: a case report","authors":"Rawan Sharma,&nbsp;Shin Miyata,&nbsp;Olivia Gentry,&nbsp;Christopher Blewett,&nbsp;Richard Herman","doi":"10.1016/j.epsc.2025.103025","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Most cases of pediatric intussusception are idiopathic, with a pathologic lead point identified in only 25 % of cases. Meckel's diverticulum (MD) is the most frequent pathologic lead point in children. The co-occurrence of intussusception and malrotation is known as Waugh's syndrome. The simultaneous presence of intestinal malrotation and intussusception due to a MD is a rare entity.</div></div><div><h3>Case presentation</h3><div>A 5-month-old girl with no significant medical history was brought to the emergency room after one day of non-bilious, non-projectile vomiting, without any rectal bleeding. A two-view abdominal x-ray was performed, showing evidence of a small bowel obstruction without bowel wall thickening or free air. Due to the non-specific findings and symptoms concerning for intussusception, an ultrasound (US) was ordered. The US suggested an ileocolic intussusception. The patient underwent an attempted pneumatic reduction (PR) with air. After three unsuccessful attempts with persistent dilated loops of small bowel the patient was taken to the operating room for surgical reduction. We did initially a laparoscopy and found dilated bowel and no colon in the right lower quadrant, which rose concern for intestinal malrotation. We decided to convert the operation to a laparotomy. We found an ileocolic intussusception, and a more proximal ileo-ileal intussusception, with a MD as the lead point, and intestinal malrotation. We did a manual reduction of both intussusceptions, resected 25 cm of small bowel containing the MD due to its ischemic appearance, did an appendectomy, and a Ladd's procedure for the malrotation. The patient recovered well postoperatively and was discharged home on postoperative day four.</div></div><div><h3>Conclusion</h3><div>Intestinal malrotation should be ruled out in patients undergoing surgical reduction of intussusception, as these two entities are occasionally associated and can present with non-typical symptoms.</div></div>","PeriodicalId":45641,"journal":{"name":"Journal of Pediatric Surgery Case Reports","volume":"118 ","pages":"Article 103025"},"PeriodicalIF":0.2000,"publicationDate":"2025-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Surgery Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213576625000703","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction

Most cases of pediatric intussusception are idiopathic, with a pathologic lead point identified in only 25 % of cases. Meckel's diverticulum (MD) is the most frequent pathologic lead point in children. The co-occurrence of intussusception and malrotation is known as Waugh's syndrome. The simultaneous presence of intestinal malrotation and intussusception due to a MD is a rare entity.

Case presentation

A 5-month-old girl with no significant medical history was brought to the emergency room after one day of non-bilious, non-projectile vomiting, without any rectal bleeding. A two-view abdominal x-ray was performed, showing evidence of a small bowel obstruction without bowel wall thickening or free air. Due to the non-specific findings and symptoms concerning for intussusception, an ultrasound (US) was ordered. The US suggested an ileocolic intussusception. The patient underwent an attempted pneumatic reduction (PR) with air. After three unsuccessful attempts with persistent dilated loops of small bowel the patient was taken to the operating room for surgical reduction. We did initially a laparoscopy and found dilated bowel and no colon in the right lower quadrant, which rose concern for intestinal malrotation. We decided to convert the operation to a laparotomy. We found an ileocolic intussusception, and a more proximal ileo-ileal intussusception, with a MD as the lead point, and intestinal malrotation. We did a manual reduction of both intussusceptions, resected 25 cm of small bowel containing the MD due to its ischemic appearance, did an appendectomy, and a Ladd's procedure for the malrotation. The patient recovered well postoperatively and was discharged home on postoperative day four.

Conclusion

Intestinal malrotation should be ruled out in patients undergoing surgical reduction of intussusception, as these two entities are occasionally associated and can present with non-typical symptoms.
梅克尔憩室致肠套叠及肠道旋转不良1例
大多数儿童肠套叠病例是特发性的,只有25%的病例有病理线索。梅克尔憩室(MD)是儿童最常见的病理先导点。肠套叠和旋转不良的同时出现被称为沃氏综合征。同时存在肠旋转不良和肠套叠由于MD是一个罕见的实体。病例介绍:一名5个月大的女婴,无明显病史,一日无胆汁、无抛射性呕吐,无直肠出血,被送往急诊室。腹部双透视显示小肠梗阻,无肠壁增厚或自由空气。由于非特异性的发现和症状有关的肠套叠,超声(美国)责令。美国提示回肠肠套叠。患者尝试用空气进行气压复位(PR)。经过三次不成功的尝试后,患者持续扩大小肠袢,被带到手术室进行手术复位。我们一开始做了腹腔镜检查,发现肠扩张,右下象限没有结肠,这引起了人们对肠道旋转不良的关注。我们决定将手术改为剖腹手术。我们发现了一个回结肠肠套叠,一个更近端的回肠-回肠肠套叠,以MD为先导点,以及肠道旋转不良。我们对两个肠套套进行了手工复位,切除了25厘米的小肠,由于其缺血的外观,切除了含有MD的小肠,做了阑尾切除术,并为旋转不良做了Ladd手术。患者术后恢复良好,于术后第4天出院。结论肠套叠手术复位患者应排除肠道旋转不良,因为这两种情况偶尔会出现,并可能出现非典型症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信