Aishath Azna Ali, F. Hayati, N. Azizan, Che Ismail Che Noh, Marjmin Osman
{"title":"胆囊胆道闭锁:梗阻性黄疸的延迟诊断","authors":"Aishath Azna Ali, F. Hayati, N. Azizan, Che Ismail Che Noh, Marjmin Osman","doi":"10.5336/caserep.2017-58558","DOIUrl":null,"url":null,"abstract":"Cystic biliary atresia is an uncommon variant of biliary atresia. It is the most usual cause of neonatal jaundice which requires surgical intervention and liver transplantation in children. Herein, we present a case of a 2-month-old baby with persistent obstructive jaundice, who was not properly investigated prior to this. After the diagnosis has been established, we proceeded with the Kasai-type portoenterostomy. Even slightly delayed, the patient recovered well postoperatively and subsequently jaundice resolved.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"41 1","pages":"102-104"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cystic Biliary Atresia: A Delayed Diagnosis of Obstructive Jaundice\",\"authors\":\"Aishath Azna Ali, F. Hayati, N. Azizan, Che Ismail Che Noh, Marjmin Osman\",\"doi\":\"10.5336/caserep.2017-58558\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Cystic biliary atresia is an uncommon variant of biliary atresia. It is the most usual cause of neonatal jaundice which requires surgical intervention and liver transplantation in children. Herein, we present a case of a 2-month-old baby with persistent obstructive jaundice, who was not properly investigated prior to this. After the diagnosis has been established, we proceeded with the Kasai-type portoenterostomy. Even slightly delayed, the patient recovered well postoperatively and subsequently jaundice resolved.\",\"PeriodicalId\":23460,\"journal\":{\"name\":\"Türkiye Klinikleri Journal of Case Reports\",\"volume\":\"41 1\",\"pages\":\"102-104\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Türkiye Klinikleri Journal of Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5336/caserep.2017-58558\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Türkiye Klinikleri Journal of Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5336/caserep.2017-58558","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Cystic Biliary Atresia: A Delayed Diagnosis of Obstructive Jaundice
Cystic biliary atresia is an uncommon variant of biliary atresia. It is the most usual cause of neonatal jaundice which requires surgical intervention and liver transplantation in children. Herein, we present a case of a 2-month-old baby with persistent obstructive jaundice, who was not properly investigated prior to this. After the diagnosis has been established, we proceeded with the Kasai-type portoenterostomy. Even slightly delayed, the patient recovered well postoperatively and subsequently jaundice resolved.