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Risk stratification in autoimmune cholestatic liver diseases: Opportunities for clinicians and trialists.自身免疫性胆汁淤积性肝病的风险分层:临床医生和试验研究者面临的机遇
Hepatology. 2016 Feb;63(2):644-59. doi: 10.1002/hep.28128. Epub 2015 Nov 26.
2
Efficacy of obeticholic acid in patients with primary biliary cirrhosis and inadequate response to ursodeoxycholic acid.奥贝胆酸治疗原发性胆汁性胆管炎患者对熊去氧胆酸应答不足的疗效。
Gastroenterology. 2015 Apr;148(4):751-61.e8. doi: 10.1053/j.gastro.2014.12.005. Epub 2014 Dec 11.
3
Clinical profile of primary biliary cirrhosis with features of autoimmune hepatitis: Importance of corticosteroid therapy.原发性胆汁性肝硬化伴有自身免疫性肝炎特征的临床特征:皮质类固醇治疗的重要性。
Hepatol Res. 2014 Sep;44(9):947-55. doi: 10.1111/hepr.12210. Epub 2013 Aug 19.
4
Sex and age are determinants of the clinical phenotype of primary biliary cirrhosis and response to ursodeoxycholic acid.性别和年龄是原发性胆汁性肝硬化临床表型和熊去氧胆酸反应的决定因素。
Gastroenterology. 2013 Mar;144(3):560-569.e7; quiz e13-4. doi: 10.1053/j.gastro.2012.12.005. Epub 2012 Dec 12.
5
Overlap syndromes: the International Autoimmune Hepatitis Group (IAIHG) position statement on a controversial issue.重叠综合征:国际自身免疫性肝炎组织(IAIHG)关于一个有争议问题的立场声明。
J Hepatol. 2011 Feb;54(2):374-85. doi: 10.1016/j.jhep.2010.09.002. Epub 2010 Sep 18.
6
Autoantibodies as prognostic markers in autoimmune liver disease.自身抗体作为自身免疫性肝病的预后标志物。
Dig Dis Sci. 2010 Aug;55(8):2144-61. doi: 10.1007/s10620-010-1268-4. Epub 2010 May 13.
7
EASL Clinical Practice Guidelines: management of cholestatic liver diseases.欧洲肝脏研究学会临床实践指南:胆汁淤积性肝病的管理
J Hepatol. 2009 Aug;51(2):237-67. doi: 10.1016/j.jhep.2009.04.009. Epub 2009 Jun 6.
8
Anti-gp210 and anti-centromere antibodies are different risk factors for the progression of primary biliary cirrhosis.抗糖蛋白210抗体和抗着丝粒抗体是原发性胆汁性肝硬化进展的不同危险因素。
Hepatology. 2007 Jan;45(1):118-27. doi: 10.1002/hep.21472.
9
International Autoimmune Hepatitis Group Report: review of criteria for diagnosis of autoimmune hepatitis.国际自身免疫性肝炎小组报告:自身免疫性肝炎诊断标准综述
J Hepatol. 1999 Nov;31(5):929-38. doi: 10.1016/s0168-8278(99)80297-9.
10
Frequency and nature of the variant syndromes of autoimmune liver disease.自身免疫性肝病变异综合征的频率及性质
Hepatology. 1998 Aug;28(2):360-5. doi: 10.1002/hep.510280210.

自身免疫性肝病:评估重叠和交叉表现——基于病例的讨论

Autoimmune liver disease: evaluating overlapping and cross-over presentations-a case-based discussion.

作者信息

Corrigan Margaret, Hirschfield Gideon M

机构信息

NIHR Birmingham Liver Biomedical Research Unit, University of Birmingham, Birmingham, UK.

Queen Elizabeth Hospital, Birmingham, UK.

出版信息

Frontline Gastroenterol. 2016 Oct;7(4):240-245. doi: 10.1136/flgastro-2016-100698. Epub 2016 Jun 8.

DOI:10.1136/flgastro-2016-100698
PMID:28839864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5369510/
Abstract

The three classic autoimmune liver diseases are recognised based on identifying varying clinical, laboratory, histological and radiological features that collectively classify patients. In the absence of defined aetiological factors, it is recognised that disease spectrum is broad, and, in this context, it is not infrequent for disease boundaries to be blurred, leading to overlapping features that may be present at the time of diagnosis or may appear later in the course of disease. Given the absence of accepted diagnostic criteria for overlap/cross-over syndromes, alongside weak data for intervention, it is recommended that a multidisciplinary, patient-specific approach be used to establish individual treatment pathways.

摘要

三种经典的自身免疫性肝病是根据识别不同的临床、实验室、组织学和放射学特征来确定的,这些特征共同对患者进行分类。在缺乏明确病因的情况下,人们认识到疾病谱很广,在这种情况下,疾病界限模糊并不罕见,这导致在诊断时可能出现重叠特征,或者在疾病过程中稍后出现。鉴于缺乏针对重叠/交叉综合征的公认诊断标准,以及干预数据不足,建议采用多学科、针对患者个体的方法来建立个体化治疗途径。