日本小児外科学会雑誌
Online ISSN : 2187-4247
Print ISSN : 0288-609X
ISSN-L : 0288-609X
先天性胆道閉塞(鎖)症の特殊型(亜型d)についての検討
千葉 庸夫望月 泉大井 龍司
著者情報
ジャーナル フリー

1987 年 23 巻 3 号 p. 530-534

詳細
抄録
During 13 years between 1972 through 1985, 129 patients with biliary atresia were treated at the Tohoku University Hospital. Nine of them showed special form (subtype "d") of obstruction of extrahepatic bile duct. They can be divided into 3 groups. Group 1: Type III biliary atresia with large cystic dilatation of choledochus, Group 2: Type II and III biliary atresia with small cystic dilatation of choledochus which was surrounded by thick fibrous tissue, Group 3: Type III biliary atresia with solitary small cyst at hepatic duct or choledochus. Postoperative course was uneventful incases of group 1. All patients in group 2 showed prolonged jaundice, and the patients in group 3 showed high portal pressure at the time of operation. Mutual relationship among subtypes was suggested by their clinical and histological findings.
著者関連情報
© 1987 特定非営利活動法人 日本小児外科学会

この記事はクリエイティブ・コモンズ [表示 - 非営利 - 継承 4.0 国際]ライセンスの下に提供されています。
https://creativecommons.org/licenses/by-nc-sa/4.0/deed.ja
前の記事 次の記事
feedback
Top