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自身免疫性肝炎诊治——病理必不可缺

王丽 杨永峰

引用本文:
Citation:

自身免疫性肝炎诊治——病理必不可缺

DOI: 10.3969/j.issn.1001-5256.2023.03.004
基金项目: 

国家自然科学基金 (81970454)

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:王丽负责检索文献,撰写文章;杨永峰负责设计文章框架,文献检索策略,修改和审核文章。
详细信息
    通信作者:

    杨永峰,yyf1997@163.com(ORCID: 0000-0002-3214-0038)

Diagnosis and treatment of autoimmune hepatitis: The indispensable role of pathology

Research funding: 

National Natural Science Foundation of China (81970454)

More Information
    Corresponding author: YANG Yongfeng, yyf1997@163.com (ORCID: 0000-0002-3214-0038)
  • 摘要: 自身免疫性肝炎现已成为国内主要的非感染性肝炎类型,本文从临床及病理角度归纳并论述了其特征性表现及诊治现状,总结出病理组织学在自身免疫性肝炎诊治中必不可缺的地位。

     

  • 图  1  慢性发病AIH病理特征(HE染色)

    注:a, 界面性肝炎(×10);b, 浆细胞浸润,箭头示浆细胞(×40);c, 玫瑰花结(×40);d, 箭头示淋巴细胞穿入(×40)。

    Figure  1.  Pathological characteristics of chronic AIH (HE staining)

    表  1  依据小叶及汇管区炎症表现的AIH诊断标准

    Table  1.   Histological criteria of AIH based on lobular and portal inflammation

    项目 汇管区炎 小叶炎
    极可能的AIH 汇管区淋巴-浆细胞浸润+以下1种或2种特征: (1)轻度以上界面炎; (2)轻度以上小叶炎
    排除提示其他肝病的组织学特征
    轻度以上小叶炎(伴或不伴小叶中心性坏死)+以下至少1种特征: (1)淋巴-浆细胞浸润; (2)界面炎; (3)汇管区纤维化
    排除提示其他肝病的组织学特征
    可能的AIH 汇管区淋巴-浆细胞浸润
    ·不具有上述1种或2种极可能的特征之一
    ·排除提示其他肝病的组织学特征或
    ·具有上述1种或2种极可能的特征
    ·存在提示其他肝病的组织学特征
    任何小叶炎(伴或不伴小叶中心性坏死)
    ·不具有上述1~3种极可能的特征之一
    ·排除提示其他肝病的组织学特征或
    ·具有上述任何1种极可能的特征
    ·存在提示其他肝病的组织学特征
    不可能的AIH 汇管区炎
    ·不具有上述1种或2种极可能的特征之一
    ·存在提示其他肝病的组织学特征
    小叶型肝炎
    ·不具有上述任何极可能的特征
    ·存在提示其他肝病的组织学特征
    下载: 导出CSV
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  • 收稿日期:  2022-12-31
  • 录用日期:  2023-02-07
  • 出版日期:  2023-03-20
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