https://scholars.lib.ntu.edu.tw/handle/123456789/537030
Title: | Autoimmune hepatitis | Authors: | Mieli-Vergani G. Heller S. Jara P. Vergani D. MEI-HWEI CHANG Fujisawa T. Gonz?lez-Peralta R.P. Kelly D. Mohan N. Shah U. Murray K.F. |
Keywords: | Autoimmune hepatitis; Hepatitis; Immunosuppression; Liver disease; Pediatrics | Issue Date: | 2009 | Journal Volume: | 49 | Journal Issue: | 2 | Start page/Pages: | 158-164 | Source: | Journal of Pediatric Gastroenterology and Nutrition | Abstract: | Autoimmune hepatitis is characterized by inflammatory liver histology, circulating nonorgan-specific autoantibodies, and increased levels of immunoglobulin G, in the absence of a known etiology. Two types of juvenile autoimmune hepatitis (AIH) are recognized according to seropositivity for smooth muscle and/or anti-nuclear antibody (AIH type 1) or liver kidney microsomal antibody (AIH type 2). There is a female predominance in both. AIH type 2 presents more acutely, at a younger age and commonly with immunoglobulin A deficiency, whereas duration of symptoms before diagnosis, clinical signs, family history of autoimmunity, presence of associated autoimmune disorders, response to treatment, and long-term prognosis are similar in the 2 groups. Immunosuppressive treatment with steroids and azathioprine, which should be instituted promptly to avoid progression to cirrhosis, induces remission in 80% of cases. Relapses are common, often due to nonadherence. Drugs effective in refractory cases include cyclosporine and mycophenolate mofetil. Long-term treatment is usually required, with only some 20% of AIH type 1 patients able to discontinue therapy successfully. In childhood, sclerosing cholangitis with strong autoimmune features, including interface hepatitis and serological features identical to AIH type 1, is as prevalent as AIH, but it affects boys and girls equally. Differential diagnosis relies on cholangiographic studies. In autoimmune sclerosing cholangitis liver parenchymal damage responds satisfactorily to immunosuppressive treatment, whereas bile duct disease tends to progress. In this article we review the state of the art of diagnosis, monitoring, and treatment for children with AIH. ? 2009 Lippincott Williams & Wilkins, Inc. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-68949151581&doi=10.1097%2fMPG.0b013e3181a1c265&partnerID=40&md5=a8d61c84a62a6652d78427c145b80923 https://scholars.lib.ntu.edu.tw/handle/123456789/537030 |
ISSN: | 0277-2116 | DOI: | 10.1097/MPG.0b013e3181a1c265 | SDG/Keyword: | 6 methylthioinosine; aminotransferase; antinuclear antibody; azathioprine; budesonide; cyclosporin A; immunoglobulin G; liver antigen; mycophenolic acid 2 morpholinoethyl ester; prednisolone; smooth muscle antibody; tacrolimus; thiopurine methyltransferase; tioguanine; ursodeoxycholic acid; aminotransferase blood level; antibody titer; autoimmune hepatitis; B lymphocyte; brain disease; cell proliferation; cholangiography; clinical assessment; diagnostic procedure; diarrhea; differential diagnosis; disease association; disease classification; disease severity; dizziness; drug blood level; drug dose increase; drug metabolism; drug withdrawal; enteritis; graft dysfunction; hair loss; headache; human; immunoglobulin A deficiency; immunosuppressive treatment; liver biopsy; liver cirrhosis; liver function test; liver toxicity; liver transplantation; long term care; nausea; neutropenia; onset age; priority journal; prognosis; recurrent disease; relapse; remission; review; sclerosing cholangitis; sex ratio; T lymphocyte; treatment duration; treatment response; Adolescent; Child; Female; Hepatitis, Autoimmune; Humans; Immunosuppressive Agents; Liver Transplantation; Male; Prednisolone |
Appears in Collections: | 醫學系 |
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