An Unknown Complication of a Rare Combination of Intestinal Invagination and Meckel’s Diverticulum Invaginated in An Adult: A Case Report

S. Ragazzi, A. Buttafuoco, S. Dipietro
{"title":"An Unknown Complication of a Rare Combination of Intestinal Invagination and Meckel’s Diverticulum Invaginated in An Adult: A Case Report","authors":"S. Ragazzi, A. Buttafuoco, S. Dipietro","doi":"10.59657/2993-1126.brs.23.008","DOIUrl":null,"url":null,"abstract":"Introduction: Intestinal invagination is a common pathology amongst children, while it is a rare entity in adults. Invagination is responsible for only 1-3% of adult-onset intestinal obstruction. Meckel’s diverticulum, on the other hand, is the most common congenital anomaly of the gastrointestinal tract. Most of them are asymptomatic; they are recognized when they complicate, and can present with diverticulitis, gastrointestinal bleeding, intestinal obstruction, perforation, or invagination. Invagination with the Meckel’s diverticulum (MD) is a rare cause of chronic abdominal pain in the adults. We wish to present this first case of intestinal invagination and Meckel ‘s diverticulum invaginated. Presentation of case: We report the case of a 17-year-old man who was admitted to the emergency room due to a diffuse abdominal pain. Abdominal CT scan showed intestinal invagination and intestinal obstruction. The exploratory laparoscopy revealed the presence of intestinal invagination and segmental resection of the small intestine was performed. The patient was discharged on the sixteen post-operative day. Discussion: The prevalence of MD is 1 to 4%. Diagnosis is often difficult and delayed because clinical symptoms are not specific and the diagnosis is performed mainly by imaging studies. Intestinal obstruction is a more common complication in adults, whereas in children, bleeding is the more common complication. In our case, the patient had a diffuse abdominal pain with small bowel obstruction. Laparoscopy may be useful for confirming the presence of intestinal invagination, and demonstrating the underlying organic lesion serving as the lead point. Only with the laparotomy we have been able to notice the combination of intestinal invagination and MD invaginated. Conclusion: we aimed to present the role of Meckel’s diverticulum as an initiating factor of illegible invagination, with inversion into the ileum and specifically in our clinical case can cause invagination of itself.","PeriodicalId":117554,"journal":{"name":"Journal of Surgical Case Reports and Reviews","volume":"101 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Surgical Case Reports and Reviews","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.59657/2993-1126.brs.23.008","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Intestinal invagination is a common pathology amongst children, while it is a rare entity in adults. Invagination is responsible for only 1-3% of adult-onset intestinal obstruction. Meckel’s diverticulum, on the other hand, is the most common congenital anomaly of the gastrointestinal tract. Most of them are asymptomatic; they are recognized when they complicate, and can present with diverticulitis, gastrointestinal bleeding, intestinal obstruction, perforation, or invagination. Invagination with the Meckel’s diverticulum (MD) is a rare cause of chronic abdominal pain in the adults. We wish to present this first case of intestinal invagination and Meckel ‘s diverticulum invaginated. Presentation of case: We report the case of a 17-year-old man who was admitted to the emergency room due to a diffuse abdominal pain. Abdominal CT scan showed intestinal invagination and intestinal obstruction. The exploratory laparoscopy revealed the presence of intestinal invagination and segmental resection of the small intestine was performed. The patient was discharged on the sixteen post-operative day. Discussion: The prevalence of MD is 1 to 4%. Diagnosis is often difficult and delayed because clinical symptoms are not specific and the diagnosis is performed mainly by imaging studies. Intestinal obstruction is a more common complication in adults, whereas in children, bleeding is the more common complication. In our case, the patient had a diffuse abdominal pain with small bowel obstruction. Laparoscopy may be useful for confirming the presence of intestinal invagination, and demonstrating the underlying organic lesion serving as the lead point. Only with the laparotomy we have been able to notice the combination of intestinal invagination and MD invaginated. Conclusion: we aimed to present the role of Meckel’s diverticulum as an initiating factor of illegible invagination, with inversion into the ileum and specifically in our clinical case can cause invagination of itself.
成人肠内陷合并梅克尔憩室罕见并发症1例报告
简介:肠内陷是一种常见的病理在儿童,而它是一个罕见的实体在成人。内陷仅占成人发病肠梗阻的1-3%。另一方面,梅克尔憩室是胃肠道最常见的先天性异常。他们大多数是无症状的;当它们出现并发症时,可被识别,并可表现为憩室炎、胃肠道出血、肠梗阻、穿孔或内陷。内陷与梅克尔憩室(MD)是一个罕见的原因慢性腹痛在成人。我们希望提出第一例肠内陷和梅克尔憩室内陷。病例介绍:我们报告一名17岁男子因弥漫性腹痛而被送往急诊室的病例。腹部CT显示肠内陷及肠梗阻。探查腹腔镜检查发现存在肠内陷和小肠节段性切除。患者于术后16天出院。讨论:MD的患病率为1% ~ 4%。诊断往往是困难和延迟的,因为临床症状不具体,诊断主要是通过影像学检查。肠梗阻是成人更常见的并发症,而在儿童中,出血是更常见的并发症。在我们的病例中,患者有弥漫性腹痛伴小肠梗阻。腹腔镜可能有助于确认肠内陷的存在,并显示潜在的器质性病变作为先导点。只有在剖腹手术中,我们才能够注意到肠内陷和MD内陷的结合。结论:我们的目的是展示Meckel憩室作为难以判读内陷的起始因素的作用,其内陷进入回肠,特别是在我们的临床病例中可引起自身内陷。
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
自引率
0.00%
发文量
0
×
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