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共同通道综合征——经内镜逆行胰胆管造影诊断及外科治疗

Common channel syndrome--diagnosis with endoscopic retrograde cholangiopancreatography and surgical management.

作者信息

Okada A, Oguchi Y, Kamata S, Ikeda Y, Kawashima Y, Saito R

出版信息

Surgery. 1983 May;93(5):634-42.

PMID:6845169
Abstract

Six patients with intermittent bouts of vomiting, fever, abdominal pain, and jaundice beginning in infancy or early childhood were all demonstrated by endoscopic retrograde cholangiopancreatography to have an anomalous junction of the pancreaticobiliary ductal system with the formation of a characteristic long common channel. A varying degree of dilatation of the bile duct also was noted. Resection of choledochus followed by hepaticoduodenostomy was performed with satisfactory results invariably in all cases. The existence of a pathologic entity that might reasonably be designated "common channel syndrome" is discussed with some comments on its relationship with dilatation of the bile duct (choledochal cyst) as well as on the recommendable method of surgical treatment.

摘要

6例自婴儿期或儿童早期开始出现间歇性呕吐、发热、腹痛及黄疸的患者,经内镜逆行胰胆管造影均显示胰胆管系统存在异常连接,并形成特征性的长共同通道。还注意到胆管有不同程度的扩张。所有病例均行胆总管切除并肝十二指肠吻合术,结果均令人满意。本文讨论了一种可合理命名为“共同通道综合征”的病理实体的存在,并对其与胆管扩张(胆总管囊肿)的关系以及推荐的手术治疗方法进行了一些评论。

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