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BACKGROUND: Congenital choledochal cyst is a rare kind of bile duct deformity, resulting from cystic or shuttle-like dilation of part of the choledochal duct congenitally. We present a 20-year-old girl with a congenital choledochal cyst complicated by acute pancreatitis. METHOD: The clinical data of the woman with a conge- nital choledochal cyst concurrent with acute pancreatitis were retrospectively analyzed. RESULT: The congenital choledochal cyst of the woman was type complicated by acute pancreatitis. CONCLUSIONS: The diagnosis of congenital choledochal cyst mainly depends on CT, MRCP, and ERCP. Total ex- cision of the choledochal cyst with Roux-en-Y hepaticoje- junostomy is recommended as the treatment. For patients with type cysts with frequently recurrent cholangitis re- sulting biliary liver cirrhosis, liver transplantation should be considered.
BACKGROUND: Congenital choledochal cyst is a rare kind of bile duct deformity, resulting from cystic or shuttle-like dilation of part of the choledochal duct congenitally. We present a 20-year-old girl with a congenital choledochal cyst complicated by acute pancreatitis. : The clinical data of the woman with a conge- nital choledochal cyst concurrent with acute pancreatitis were retrospectively analyzed. RESULT: The congenital choledochal cyst of the woman was type complicated by acute pancreatitis. CONCLUSIONS: The diagnosis of congenital choledochal cyst mainly depends on CT , MRCP, and ERCP. Total ex-cision of the choledochal cyst with Roux-en-Y hepaticoje-junostomy is recommended as the treatment. For patients with type cysts with frequently recurrent cholangitis re- sulting biliary liver cirrhosis, liver transplantation should be considered .