重视不典型自身免疫性肝病患者的早诊早治
DOI: 10.3969/j.issn.1001-5256.2022.04.003
利益冲突声明:所有作者均声明不存在利益冲突。
作者贡献声明:黄春洋参与文章的撰写、修改;刘燕敏负责文章的思路框架设计、文章撰写校稿。
The early diagnosis and treatment of atypical autoimmune liver disease should be taken seriously
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摘要: 自身免疫性肝病是一组疾病,主要由于自身免疫异常引起,包括以肝细胞损伤为主的自身免疫性肝炎,以胆管损伤为主的原发性胆汁性胆管炎及原发性硬化性胆管炎,也包括具有上述两种疾病主要特征的重叠综合征,近来IgG4相关肝胆疾病也被列入此类,如不及时诊治,可发展至肝硬化,甚至肝衰竭。自身免疫性肝病均有各自特点,随着自身免疫性肝病知识普及,专业医生对此类疾病认识程度逐渐增加,多数较典型自身免疫性肝病能够早期诊断,使患者得到及时治疗。但也有一些患者表现或化验指标不典型,易被延误诊断,所以对于不典型自身免疫性肝病及早辨别,及时诊治非常重要。Abstract: Autoimmune liver disease is a group of diseases mainly caused by autoimmune abnormalities, including autoimmune hepatitis dominated by hepatocellular injury, primary biliary cholangitis and primary sclerosing cholangitis dominated by bile duct injury, and overlap syndrome with the main features of the above two diseases. Recently, IgG4-related hepatobiliary diseases have also been included in this category, and without timely diagnosis and treatment, it can progress to liver cirrhosis and even liver failure. Different autoimmune liver diseases have their own features, and with the popularization of the knowledge on autoimmune liver diseases, physicians have gradually increased their understanding of such diseases and can achieve the early diagnosis and timely treatment of most typical autoimmune liver diseases. However, some patients may have atypical manifestations or laboratory markers, which may easily delay the diagnosis, and therefore, it is of great importance to identify atypical autoimmune liver disease and give timely diagnosis and treatment as soon as possible.
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