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胆道闭锁

Biliary atresia.

作者信息

Ohi R, Ibrahim M

机构信息

Department of Pediatric Surgery, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Semin Pediatr Surg. 1992 May;1(2):115-24.

PMID:1345477
Abstract

Although biliary atresia is characterized by luminal obstruction of the extrahepatic bile ducts, the etiology and the pathophysiology of the liver are still controversial. The prognosis of biliary atresia has been improved after the introduction of Kasai's hepatic portoenterostomy, but there are still many problems to be solved in the treatment of this disease. Successful results of hepatic portoenterostomy depend on early diagnosis and operation, adequate operative technique, prevention of postoperative cholangitis, and precise postoperative management. However, we are on the verge of a new era in the therapy of biliary atresia combining portoenterostomy with liver transplantation.

摘要

尽管胆道闭锁的特征是肝外胆管管腔阻塞,但肝脏的病因和病理生理学仍存在争议。自从开展了Kasai肝门肠吻合术后,胆道闭锁的预后有所改善,但在这种疾病的治疗中仍有许多问题有待解决。肝门肠吻合术的成功结果取决于早期诊断和手术、适当的手术技术、术后胆管炎的预防以及精确的术后管理。然而,我们正处在一个将肝门肠吻合术与肝移植相结合治疗胆道闭锁的新时代的边缘。

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