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[胆道闭锁:肝脏实质组织病理学分析中出现的发病机制思考]

[Biliary atresia: pathogenetic considerations emerging from the histopathologic analysis of the liver parenchyma].

作者信息

Farolfi A, Cattaneo M, Varenna R, Portaleone D, Ferrentino R, Carnelli V

出版信息

Pediatr Med Chir. 1983 May-Jun;5(3):69-73.

PMID:6647066
Abstract

Nine patients had been surgically treated for extrahepatic biliary atresia from 1974 to 1982. The analysis of the hepatic specimens obtained during the surgical exploration revealed a wide spectrum of histopathologic lesions. In 3 patients we found severe Giant-cell transformation, while in the other 6 it was not possible to ascribe the histopathologic picture to a univocal pathogenesis. Comparing our results to the reports of other Authors we believe biliary atresia can not be explained by a single pathologic mechanism. The obstruction of the extrahepatic bile ducts might be the common morphologic denominator of different pathologic entities, from each of them it depends a different evolution of the hepatic lesions and a different survival after Kasai's operation.

摘要

1974年至1982年期间,有9例患者接受了肝外胆道闭锁的手术治疗。对手术探查时获取的肝脏标本进行分析后发现,存在广泛的组织病理学病变。在3例患者中,我们发现了严重的巨细胞转化,而在其他6例中,无法将组织病理学表现归因于单一的发病机制。将我们的结果与其他作者的报告进行比较后,我们认为胆道闭锁不能用单一的病理机制来解释。肝外胆管阻塞可能是不同病理实体的共同形态学特征,肝脏病变的不同演变以及Kasai手术后的不同生存率均取决于其中的每一种病理实体。

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