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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
  • [1] LIU HL, YANG YF, XIONG QF, et al. Etiological analysis of hepatopathy of unknown etiology in 470 cases undergoing routine liver biopsy examination[J]. Chin J Hepatol, 2019, 27(11): 885-889. DOI: 10.3760/cma.j.issn.1007-3418.2019.11.012.

    刘红丽, 杨永峰, 熊清芳, 等. 470例行肝穿刺活组织检查的不明原因肝病的病因分析[J]. 中华肝脏病杂志, 2019, 27(11): 885-889. DOI: 10.3760/cma.j.issn.1007-3418.2019.11.012.
    [2] ZHANG HY, MA X. Diagnosis and management of autoimmune hepatitis with acute presentation[J]. Chin J Hepatol, 2012, 20(5): 396-397. DOI: 10.3760/cma.j.issn.1007-3418.2012.05.021.

    张海燕, 马雄. 急性起病自身免疫性肝炎的诊断与治疗[J]. 中华肝脏病杂志, 2012, 20(5): 396-397. DOI: 10.3760/cma.j.issn.1007-3418.2012.05.021.
    [3] LI YN, MA H, ZHOU L, et al. Autoimmune hepatitis-related cirrhosis: clinical features and effectiveness of immunosuppressive treatment in chinese patients[J]. Chin Med J (Engl), 2016, 129(20): 2434-2440. DOI: 10.4103/0366-6999.191760.
    [4] VILLALTA D, GIROLAMI E, ALESSIO MG, et al. Autoantibody profiling in a cohort of pediatric and adult patients with autoimmune hepatitis[J]. J Clin Lab Anal, 2016, 30(1): 41-46. DOI: 10.1002/jcla.21813.
    [5] GORDON V, ADHIKARY R, APPLEBY V, et al. Diagnosis, presentation and initial severity of Autoimmune Hepatitis (AIH) in patients attending 28 hospitals in the UK[J]. Liver Int, 2018, 38(9): 1686-1695. DOI: 10.1111/liv.13724.
    [6] SEBODE M, WEILER-NORMANN C, LIWINSKI T, et al. Autoantibodies in autoimmune liver disease-clinical and diagnostic relevance[J]. Front Immunol, 2018, 9: 609. DOI: 10.3389/fimmu.2018.00609.
    [7] TERZIROLI BERETTA-PICCOLI B, MIELI-VERGANI G, et al. Autoimmune hepatitis: Serum autoantibodies in clinical practice[J]. Clin Rev Allergy Immunol, 2022, 63(2): 124-137. DOI: 10.1007/s12016-021-08888-9.
    [8] GATSELIS NK, ZACHOU K, KOUKOULIS GK, et al. Autoimmune hepatitis, one disease with many faces: etiopathogenetic, clinico-laboratory and histological characteristics[J]. World J Gastroenterol, 2015, 21(1): 60-83. DOI: 10.3748/wjg.v21.i1.60.
    [9] YANG XJ, YANG YF, ZHONG YD. The value of serum immunoglobulin and autoantibodies in the diagnosis of autoimmune hepatitis[J]. Chin Hepatol, 2018, 23(12): 1084-1086. DOI: 10.14000/j.cnki.issn.1008-1704.2018.12.012.

    杨小娇, 杨永峰, 钟艳丹. 血清免疫球蛋白与自身抗体检测在自身免疫性肝炎诊断中的价值[J]. 肝脏, 2018, 23(12): 1084-1086. DOI: 10.14000/j.cnki.issn.1008-1704.2018.12.012.
    [10] MIAO Q, CHEN XY. Liver histopathological diagnosis of autoimmune hepatitis[J]. J Clin Hepatol, 2020, 36(4): 728-730. DOI: 10.3969/j.issn.1001-5256.2020.04.003.

    苗琪, 陈晓宇. 自身免疫性肝炎的肝组织病理学诊断[J]. 临床肝胆病杂志, 2020, 36(4): 728-730. DOI: 10.3969/j.issn.1001-5256.2020.04.003.
    [11] NGUYEN CANH H, HARADA K, OUCHI H, et al. Acute presentation of autoimmune hepatitis: a multicentre study with detailed histological evaluation in a large cohort of patients[J]. J Clin Pathol, 2017, 70(11): 961-969. DOI: 10.1136/jclinpath-2016-204271.
    [12] AIZAWA Y, ABE H, SUGITA T, et al. Centrilobular zonal necrosis as a hallmark of a distinctive subtype of autoimmune hepatitis[J]. Eur J Gastroenterol Hepatol, 2016, 28(4): 391-397. DOI: 10.1097/MEG.0000000000000545.
    [13] WANG PS, WANG JY, HU XQ, et al. Clinical and histopathologic features of drug-induced autoimmune hepatitis[J]. Chin J Dig, 2014, 34(2): 105-108. DOI: 10.3760/cma.j.issn.0254-1432.2014.02.008.

    王丕胜, 王吉耀, 胡锡琪, 等. 药物诱导的自身免疫性肝炎的临床和病理特点[J]. 中华消化杂志, 2014, 34(2): 105-108. DOI: 10.3760/cma.j.issn.0254-1432.2014.02.008.
    [14] BJÖRNSSON ES, NAVARRO VJ, CHALASANI N. Liver injury following tinospora cordifolia consumption: Drug-Induced AIH, or de novo AIH?[J]. J Clin Exp Hepatol, 2022, 12(1): 6-9. DOI: 10.1016/j.jceh.2021.11.014.
    [15] FEBRES-ALDANA CA, ALGHAMDI S, KRISHNAMURTHY K, et al. Liver fibrosis helps to distinguish autoimmune hepatitis from DILI with autoimmune features: A review of twenty cases[J]. J Clin Transl Hepatol, 2019, 7(1): 21-26. DOI: 10.14218/JCTH.2018.00053.
    [16] TSUTSUI A, HARADA K, TSUNEYAMA K, et al. Histopathological analysis of autoimmune hepatitis with "acute" presentation: Differentiation from drug-induced liver injury[J]. Hepatol Res, 2020, 50(9): 1047-1061. DOI: 10.1111/hepr.13532.
    [17] ALVAREZ F, BERG PA, BIANCHI FB, et al. International autoimmune hepatitis group report: review of criteria for diagnosis of autoimmune hepatitis[J]. J Hepatol, 1999, 31(5): 929-938. DOI: 10.1016/s0168-8278(99)80297-9.
    [18] HENNES EM, ZENIYA M, CZAJA AJ, et al. Simplified criteria for the diagnosis of autoimmune hepatitis[J]. Hepatology, 2008, 48(1): 169-176. DOI: 10.1002/hep.22322.
    [19] QIU D, WANG Q, WANG H, et al. Validation of the simplified criteria for diagnosis of autoimmune hepatitis in Chinese patients[J]. J Hepatol, 2011, 54(2): 340-347. DOI: 10.1016/j.jhep.2010.06.032.
    [20] LOHSE AW, SEBODE M, BHATHAL PS, et al. Consensus recommendations for histological criteria of autoimmune hepatitis from the International AIH Pathology Group: Results of a workshop on AIH histology hosted by the European Reference Network on Hepatological Diseases and the European Society of Pathology: Results of a workshop on AIH histology hosted by the European Reference Network on Hepatological Diseases and the European Society of Pathology[J]. Liver Int, 2022, 42(5): 1058-1069. DOI: 10.1111/liv.15217.
    [21] HARADA K, HIEP NC, OHIRA H. Challenges and difficulties in pathological diagnosis of autoimmune hepatitis[J]. Hepatol Res, 2017, 47(10): 963-971. DOI: 10.1111/hepr.12931.
    [22] Chinese Society of Hepatology, Chinese Medical Association. Guidelines on the diagnosis and management of autoimmune hepatitis (2021)[J]. J Clin Hepatol, 2022, 38(1): 42-49. DOI: 10.3760/cma.j.cn112138-20211112-00796.

    中华医学会肝病学分会. 自身免疫性肝炎诊断和治疗指南(2021)[J]. 临床肝胆病杂志, 2022, 38(1): 42-49. DOI: 10.3760/cma.j.cn112138-20211112-00796.
    [23] AL-CHALABI T, HENEGHAN MA. Remission in autoimmune hepatitis: what is it, and can it ever be achieved?[J]. Am J Gastroenterol, 2007, 102(5): 1013-1015. DOI: 10.1111/j.1572-0241.2007.01147.x.
    [24] HARRISON L, GLEESON D. Stopping immunosuppressive treatment in autoimmune hepatitis (AIH): Is it justified (and in whom and when)?[J]. Liver Int, 2019, 39(4): 610-620. DOI: 10.1111/liv.14051.
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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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