药物诱导的自身免疫样肝炎的临床诊断
DOI: 10.12449/JCH250322
利益冲突声明:本文不存在任何利益冲突。
作者贡献声明:刘永萍负责选题,检索文献,资料分析,撰写论文;沈瑶杰负责拟定写作思路,指导撰写文章并最后定稿。
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摘要: 药物性肝损伤(DILI)中部分病例可以表现出与自身免疫性肝炎(AIH)相似的特征,即药物诱导的自身免疫样肝炎(DI-ALH)。2022年欧洲肝病学会对DI-ALH的命名、诊断和临床处理进行了讨论并提出了专家意见,建立了临床诊断标准。然而,DI-ALH的临床诊断依然复杂、困难,药物摄入和机体免疫进展之间的联系目前尚无直接证据。因此,本文从临床表型、病理诊断、诊断积分和临床预后4个方面探讨DI-ALH诊断相关的研究进展。
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关键词:
- 药物诱导的自身免疫样肝炎 /
- 药物性肝损伤 /
- 肝炎, 自身免疫性 /
- 诊断
Abstract: Some patients with drug-induced liver injury (DILI) may present with similar features to patients with autoimmune hepatitis (AIH), and such cases are defined as drug-induced autoimmune-like hepatitis (DI-ALH). In 2022, the European Association for the Study of the Liver discussed the nomenclature, diagnosis, and treatment of DI-ALH and put forward expert opinions to establish the criteria for clinical diagnosis. However, the clinical diagnosis of DI-ALH remains complex and difficult, and there is no direct evidence for the link between drug intake and the body’s immune progression. Therefore, this article reviews the research advances in the diagnosis of DI-ALH from the four aspects of clinical phenotype, pathological diagnosis, diagnostic score, and clinical prognosis. -
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