{"title":"卡罗莱氏病:一个小回顾","authors":"McCafferty J, Li C","doi":"10.47829/jjgh.2022.8401","DOIUrl":null,"url":null,"abstract":"Caroli’s disease is a rare congenital condition that is characterised by intrahepatic biliary duct dilatation without fibrosis. It is associated with an increased risk of cholelithiasis, cholangitis and cholangiocarcinoma. As such, it is an important clinical entity to be aware of. Most of the literature surrounding Caroli’s disease is limited to case reports and case series. This review will explore the clinical characteristics, imaging modalities and management of Caroli’s disease","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":"{\"title\":\"Caroli’s Disease: A Mini-Review\",\"authors\":\"McCafferty J, Li C\",\"doi\":\"10.47829/jjgh.2022.8401\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Caroli’s disease is a rare congenital condition that is characterised by intrahepatic biliary duct dilatation without fibrosis. It is associated with an increased risk of cholelithiasis, cholangitis and cholangiocarcinoma. As such, it is an important clinical entity to be aware of. Most of the literature surrounding Caroli’s disease is limited to case reports and case series. This review will explore the clinical characteristics, imaging modalities and management of Caroli’s disease\",\"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.2022.8401\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Japanese journal of gastroenterology and hepatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47829/jjgh.2022.8401","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Caroli’s disease is a rare congenital condition that is characterised by intrahepatic biliary duct dilatation without fibrosis. It is associated with an increased risk of cholelithiasis, cholangitis and cholangiocarcinoma. As such, it is an important clinical entity to be aware of. Most of the literature surrounding Caroli’s disease is limited to case reports and case series. This review will explore the clinical characteristics, imaging modalities and management of Caroli’s disease
求助内容：
应助结果提醒方式：
京公网安备 11010802042870号
