A Rare Cause of Intestinal Obstruction: Case Report of an Abdominal Cocoon Syndrome in a Middle Aged Man from the Mediterranean Region

Jibaii S, N. Y, Bouhairie Mm, Bleibel L, Hotayt B
{"title":"A Rare Cause of Intestinal Obstruction: Case Report of an Abdominal Cocoon Syndrome in a Middle Aged Man from the Mediterranean Region","authors":"Jibaii S, N. Y, Bouhairie Mm, Bleibel L, Hotayt B","doi":"10.47829/jjgh.2022.8301","DOIUrl":null,"url":null,"abstract":"1.1. Introduction: Abdominal cocoon syndrome is a rare condition that refers to total or partial encapsulation of the small intestines leading to recurrent bowel obstruction. It usually affects young ladies from tropical and subtropical area. 1.2. Methods: we report a middle aged man, from the Mediterranean region, presenting with small bowel obstruction, with history of recurrent similar episode. 1.3. Results: after failure of conservative treatment, surgical exploration showed a thick fibrous peritoneal membrane wrapping the small bowel in a concentric fashion with some adhesions. The pathology of this resected fibrous membrane confirmed the diagnosis of an abdominal cocoon syndrome. 1.4. Conclusion: From the atypical presentation of our case, we can conclude that though rare, this condition must be kept in mind when considering the differential diagnosis of idiopathic intestinal obstruction in any adult and therefore the decision of a surgical exploration should not be differed in the appropriate context, especially in the light of the condition’s benign nature and favorable prognosis. 1.5. Background: Abdominal cocoon syndrome is a rare condition that refers to total or partial encapsulation of the small intestines by a fibro-collagenous membrane with local inflammatory infiltrate leading to acute, subacute or chronic bowel obstruction [1]. It also has been described as “encapsulating peritoneal sclerosis”, “sclerosing encapsulating peritonitis” and in Latin “peritonitis chronica fibrosaincapsulata” [1, 2]","PeriodicalId":73535,"journal":{"name":"Japanese journal of gastroenterology and hepatology","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Japanese journal of gastroenterology and hepatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47829/jjgh.2022.8301","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

1.1. Introduction: Abdominal cocoon syndrome is a rare condition that refers to total or partial encapsulation of the small intestines leading to recurrent bowel obstruction. It usually affects young ladies from tropical and subtropical area. 1.2. Methods: we report a middle aged man, from the Mediterranean region, presenting with small bowel obstruction, with history of recurrent similar episode. 1.3. Results: after failure of conservative treatment, surgical exploration showed a thick fibrous peritoneal membrane wrapping the small bowel in a concentric fashion with some adhesions. The pathology of this resected fibrous membrane confirmed the diagnosis of an abdominal cocoon syndrome. 1.4. Conclusion: From the atypical presentation of our case, we can conclude that though rare, this condition must be kept in mind when considering the differential diagnosis of idiopathic intestinal obstruction in any adult and therefore the decision of a surgical exploration should not be differed in the appropriate context, especially in the light of the condition’s benign nature and favorable prognosis. 1.5. Background: Abdominal cocoon syndrome is a rare condition that refers to total or partial encapsulation of the small intestines by a fibro-collagenous membrane with local inflammatory infiltrate leading to acute, subacute or chronic bowel obstruction [1]. It also has been described as “encapsulating peritoneal sclerosis”, “sclerosing encapsulating peritonitis” and in Latin “peritonitis chronica fibrosaincapsulata” [1, 2]
一种罕见的肠梗阻病因:地中海地区中年男子腹部茧状综合征1例报告
1.1. 简介:腹茧综合征是指小肠全部或部分包封导致肠梗阻复发的一种罕见疾病。它通常影响来自热带和亚热带地区的年轻女性。1.2. 方法:我们报告一位来自地中海地区的中年男性,表现为小肠梗阻,并有复发性类似发作的历史。1.3. 结果:保守治疗失败后,手术探查显示厚纤维性腹膜以同心方式包裹小肠并有粘连。切除纤维膜的病理证实了腹部茧综合征的诊断。1.4. 结论:从本病例的非典型表现,我们可以得出结论,尽管罕见,但在考虑任何成人特发性肠梗阻的鉴别诊断时,必须牢记这种情况,因此手术探查的决定不应在适当的情况下有所不同,特别是考虑到这种情况的良性性质和良好的预后。1.5. 背景:腹茧综合征是指小肠全部或部分被纤维胶原膜包裹,局部炎症浸润导致急性、亚急性或慢性肠梗阻的一种罕见疾病。它也被描述为“包膜性腹膜硬化”、“硬化性包膜性腹膜炎”和拉丁语“慢性纤维荚膜性腹膜炎”[1,2]
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