| Literature DB >> 28480763 |
Paolo Muratori1, Marco Lenzi1, Fabio Cassani1, Claudine Lalanne1, Luigi Muratori1.
Abstract
INTRODUCTION: Autoimmune hepatitis (AIH) is a chronic inflammatory liver disease which, if left without treatment, can evolve into cirrhosis and possibly liver failure. The diagnosis of AIH is hampered by the lack of specific and reliable markers of the disease and a number of clinical, biochemical, immunological, histological and genetic factors should be considered to reach a confident diagnosis Areas covered: Clinical expression of AIH, histological features, serological and genetic profiles, differential diagnosis, overlap with other autoimmune liver diseases, assessed on the basis of personal experience and review of published literature in the last 10 years through a systematic Medline search (keywords: autoimmune hepatitis, diagnosis) Expert commentary: Notwithstanding numerous efforts to identify simple and reliable markers of the disease, the diagnosis of AIH is still based on the combination of histological, immunological and biochemical features and often can represent a real challenge for the hepatologist.Entities:
Keywords: Autoimmune hepatitis; anti smooth muscle antibodies; antinuclear antibodies; autoantibodies; hypergammaglobulinemia; interface hepatitis; liver kidney microsome type 1; pattern
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Year: 2017 PMID: 28480763 DOI: 10.1080/1744666X.2017.1327355
Source DB: PubMed Journal: Expert Rev Clin Immunol ISSN: 1744-666X Impact factor: 4.473