| Literature DB >> 26019445 |
Caterina Anania1, Ester De Luca1, Giovanna De Castro1, Claudio Chiesa1, Lucia Pacifico1.
Abstract
Celiac disease (CD) is an intestinal inflammatory disease that manifests in genetically susceptible individuals when exposed to dietary gluten. It is a common chronic disorder, with a prevalence of 1% in Europe and North America. Although the disease primarily affects the gut, the clinical spectrum of CD is remarkably varied, and the disease can affect many extraintestinal organs and systems, including the liver. The hepatic dysfunction presenting in CD ranges from asymptomatic liver enzyme elevations or nonspecific reactive hepatitis (cryptogenic liver disorders), to chronic liver disease. In this article, we review the clinical presentations and possible mechanisms of CD-related liver injury to identify strategies for the diagnosis and treatment of these disorders in childhood.Entities:
Keywords: Autoimmune liver disease; Celiac disease; Cryptogenic hypertransaminasemia; End-stage liver disease; Fatty liver
Mesh:
Year: 2015 PMID: 26019445 PMCID: PMC4438015 DOI: 10.3748/wjg.v21.i19.5813
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742