Surgical treatment of choledochal cyst.
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This article is published in Annals of Surgery.The article was published on 1970-11-01 and is currently open access. It has received 137 citations till now. The article focuses on the topics: Choledochal cysts.read more
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Congenital bile duct cysts: Classification, operative procedures, and review of thirty-seven cases including cancer arising from choledochal cyst
TL;DR: Congenital bile duct cysts are observed in any part of the biliary duct from the liver to the duodenum and reports of cases of cancer arising from it are increasing.
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Congenital choledochal cyst. Analysis of 1,433 patients in the Japanese literature.
TL;DR: Five of the author's cases and 1,428 cases from Japan's literature are discussed, including patients with malformation of the pancreaticobiliary system, which is said to be a cause of congenital choledochal cyst.
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Bile duct cancer developed after cyst excision for choledochal cyst
TL;DR: Clinical data of 23 patients with cancer of the biliary tree after excision of choledochal cyst reported in the English-language and Japanese literature were reviewed, and data for 1353 Japanese patients with cholingochal Cyst and/or pancreaticobiliary malunion were analyzed.
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Late development of bile duct cancer in patients who had biliary-enteric drainage for benign disease: a follow-up study of more than 1,000 patients.
Adriano Tocchi,Gianluca Mazzoni,Gianluca Liotta,Luca Lepre,Diletta Cassini,Michelangelo Miccini +5 more
TL;DR: Chronic inflammatory changes consequent to biliary-enteric drainage should be closely monitored for the late development of biliary tract malignancies, as univariate and multivariate analyses have shown the presence of cholangitis as the only factor affecting the incidence of choledocholithiasis.
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Hepatobiliary fibropolycystic diseases: A clinical and histological review of 51 patients
TL;DR: In this paper, the clinical, radiological and hepatic histological features of 51 patients with hepatobiliary fibropolycystic disease were reviewed, and the combination of both congenital hepatic fibrosis (CHF) and Caroli's disease was most striking.