{"title":"胆总管囊肿伴破裂和假性囊肿形成","authors":"Reem Ichoa, Rajesh Savargaonkar, V. Jones","doi":"10.25270/con.2022.07.00003","DOIUrl":null,"url":null,"abstract":"Background. Choledochal cysts are congenital anomalies of the biliary duct. The most common site for the development of cystic dilation is the common bile duct. Although choledochal cysts are a rare disease in children, complications such as perforation of the cyst have been reported. In this literature review, we discuss a case of a choledochal cyst with rupture and pseudocyst formation. Complete excision of the cyst and pseudocyst yields an excellent outcome with a 90% 5-year survival rate postoperatively.","PeriodicalId":35575,"journal":{"name":"Consultant","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Choledochal Cyst With Rupture and Pseudocyst Formation\",\"authors\":\"Reem Ichoa, Rajesh Savargaonkar, V. Jones\",\"doi\":\"10.25270/con.2022.07.00003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background. Choledochal cysts are congenital anomalies of the biliary duct. The most common site for the development of cystic dilation is the common bile duct. Although choledochal cysts are a rare disease in children, complications such as perforation of the cyst have been reported. In this literature review, we discuss a case of a choledochal cyst with rupture and pseudocyst formation. Complete excision of the cyst and pseudocyst yields an excellent outcome with a 90% 5-year survival rate postoperatively.\",\"PeriodicalId\":35575,\"journal\":{\"name\":\"Consultant\",\"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\":\"Consultant\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.25270/con.2022.07.00003\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Consultant","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25270/con.2022.07.00003","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Choledochal Cyst With Rupture and Pseudocyst Formation
Background. Choledochal cysts are congenital anomalies of the biliary duct. The most common site for the development of cystic dilation is the common bile duct. Although choledochal cysts are a rare disease in children, complications such as perforation of the cyst have been reported. In this literature review, we discuss a case of a choledochal cyst with rupture and pseudocyst formation. Complete excision of the cyst and pseudocyst yields an excellent outcome with a 90% 5-year survival rate postoperatively.
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