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作 者:Lin-Ping Cao Xun Zhong Kang-Jie Chen Jun Yu
出 处:《Hepatobiliary & Pancreatic Diseases International》2023年第6期658-660,共3页国际肝胆胰疾病杂志(英文版)
基 金:the Natural Science Foundation of Zhejiang Province(LQ21H160025).
摘 要:To the Editor:Choledochocele,also known as type III choledochal cysts in the classification by Todani et al.[1],is a congenital abnormality of the biliary system.It is characterized by a cystic dilation of intramural segment of the distal common bile duct(CBD)protruding into the descending duodenum.Choledochocele makes up about 0.5%−4%of choledochal cysts[1,2].Compared with other subtypes,the incidence of choledochocele is extremely low and it frequently presents in adults at a relatively older age,with an average age of 51 years[3].The diagnosis and treatment are challenging.Here,we present a case of a young female patient with this rare disease entity,who recovered after effective endoscopic retrograde cholangiopancreatography(ERCP)management.
关 键 词:FEMALE RETROGRADE
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