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Vol.32 No.5 1999 May [Table of Contents] [Full text ( PDF 76KB)]
CASE REPORT

A Case of Congenital Cystic Dilatation of Bile Duct without Pancreaticobiliary Maljunction

Ei Sekoguchi, Kenji Tsuchie, Hiroshi Kuriki, Kenji Sakaguchi and Eiji Hayashi

Department of Surgery, Meijo Hospital

A 48-year-old woman, who had occasional right hypochondralgia for one year, consulted a local medical doctor. Abdominal ultrasonography was performed and showed dilatation of the common bile bile duct. There after, she was referred to our hospital, where endoscopic ultrasonography and endoscopic retrograde cholangiopancreatography were performed. A diagnosis of congenital dilatation of bile duct was made, but pancreaticobiliary maljunction was uncertain. Resection of the dilated bile duct was carried out. To determine the cut end of the distal bile duct, intraoperative cholangiography was performed, and showed no sign of pancreaticobiliary maljunction. The level of amylase value in bile juice of the bile duct was normal as 32IU/l.This case is an interesting example of the relationship between congenital dilatation of bile duct and pancreaticobiliary maljunction.

Key words
congenital dilatation of bile duct, pancreaticobiliary maljunction

Jpn J Gastroenterol Surg 32: 1213-1216, 1999

Reprint requests
Ei Sekoguchi Department of Surgery, Meijo Hospital 1-3-1 Sannomaru, Naka-ku, Nagoya, 460-0001 JAPAN

Accepted
January 27, 1999

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