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KMID : 0359019930130010133
Korean Journal of Gastrointestinal Endoscopy
1993 Volume.13 No. 1 p.133 ~ p.136
Cholangiocarcinoma Arising in Choledocal Cyst
박찬욱
문수남/이준성/이문성/김진홍/조성원/심찬섭/문철/이동화
Abstract
Choledochal cyst is a relatively rare disease entity considered to be a congenital cystic dilatation of the common bile duct. Since occurrence of malignant tumor in choledochal cyst was first reported by Irwin and Morrison in 1944, approximately
100
more cases of malignant tumors arising in congenital choledocal cyst have been reported in the world, and the risk of malignant tumor related to choledochal cyst have been reported as 2.4~14%.
Recently, we experienced a case of adenocarcinoma arising in choledochal cyst in 39 year-old woman who was diagnosed by ERCP and cholangiosocpy with forceps biopsy, and was treated with en bloc resection of the choledochal cyst along with the
pancreatic
head and duodenum.
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