丙戊酸肝毒性综合征:发病机制假说。

J R Stephens, R H Levy
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引用次数: 21

摘要

抗惊厥药丙戊酸酯(VPA)的治疗性使用与一种罕见但严重且通常致命的肝毒性有关。病例通常表现为嗜睡、厌食和呕吐,并迅速发展为昏迷。肝脏组织病理学表现为脂肪变性伴或不伴坏死。部分病例仅出现坏死。人们对发病机制提出了几种假设。这些主要涉及已知受VPA影响的生化系统,或有毒VPA代谢物,特别是- 4-VPA的可能特异性产生。目前,还没有一种假说能完全解释这种疾病的多种特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Valproate hepatotoxicity syndrome: hypotheses of pathogenesis.

Therapeutic use of the anticonvulsant valproate (VPA) has been associated with a rare, but severe and often fatal hepatotoxicity. Cases usually present with lethargy, anorexia, and vomiting with rapid progression to coma. Liver histopathology is characterized by steatosis with and without necrosis. In some instances only necrosis was present. Several hypotheses of pathogenesis have been postulated. These deal mainly with biochemical systems that are known to be affected by VPA, or with the possible idiosyncratic production of toxic VPA metabolites, especially delta 4-VPA. At present, no hypothesis entirely explains the diverse characteristics of the disorder.

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