{"title":"An Unusual Case of Painless Obstructive Jaundice and Cholangitis: Lemmel’s Syndrome- A Case Report","authors":"Praveen S. Padasali, Vinayak Thakkannavar","doi":"10.5530/OGH.2018.7.2.25","DOIUrl":null,"url":null,"abstract":"Copyright © 2018 Phcog.Net. This is an openaccess article distributed under the terms of the Creative Commons Attribution 4.0 International license. Cite this article: Padasali PS, Thakkannavar V. A Unusual Case of Painless Obstructive Jaundice and Cholangitis: Lemmel’s SyndromeA Case Report. OGH Reports. 2018;7(2):106-8. ABSTRACT A unusual case of periampullary duodenal diverticulum causing obstructive jaundice. Duodenal diverticula are detected in up to 27% of patients undergoing upper gastrointestinal endoscopy with periampullary diverticula (PAD) being the most common type. Although periampullary diverticula rarely cause obstructive jaundice when choledocholithiasis or tumor is not present. The periampullary duodenal diverticulum causing extrinsic compression of common bile duct and obstructive jaundice is called Lemmel’s syndrome. An 58-yr-old woman came to the emergency room with obstructive jaundice and cholangitis. Abdominal CT scan revealed PAD compressing distal CBD with CBD dilatation. PAD shows signs of inflammation in CT scan and Endoscopy. Recognition of this condition is important since misdiagnosis could lead to mismanagement and therapeutic delay. Whenever PAD is present it should always be included as one of the differential diagnosis of obstructive jaundice.","PeriodicalId":166206,"journal":{"name":"Oncology, Gastroenterology and Hepatology Reports","volume":"16 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oncology, Gastroenterology and Hepatology Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5530/OGH.2018.7.2.25","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
无痛性梗阻性黄疸合并胆管炎1例:Lemmel综合征1例报告
版权所有©2018phcog.net这是一篇基于知识共享署名4.0国际许可协议的开放获取文章。引用本文:Padasali PS, Thakkannavar V. 1例罕见的无痛性梗阻性黄疸和胆管炎:Lemmel综合征病例报告。卫生报告,2018;7(2):106-8。壶腹周围十二指肠憩室引起梗阻性黄疸的罕见病例。在接受上消化道内镜检查的患者中,高达27%的患者可检出十二指肠憩室,其中壶腹周围憩室(PAD)是最常见的类型。虽然壶腹周围憩室很少引起梗阻性黄疸,当胆总管结石或肿瘤不存在。壶腹周围十二指肠憩室引起胆总管外源性压迫和梗阻性黄疸称为Lemmel综合征。一名58岁妇女因梗阻性黄疸和胆管炎来到急诊室。腹部CT扫描显示PAD压迫CBD远端伴CBD扩张。PAD在CT扫描和内窥镜检查中显示炎症征象。认识到这种情况是很重要的,因为误诊可能导致管理不善和治疗延误。无论何时出现PAD,都应作为阻塞性黄疸的鉴别诊断之一。
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