Autoimmune liver disease: Novelties in management

被引:8
|
作者
Hadzic, Nedim [1 ]
Hierro, Loreto [2 ]
机构
[1] Kings Coll Hosp London, Pediat Ctr Hepatol Gastroenterol & Nutr, London, England
[2] La Paz Childrens Univ Hosp, Pediat Liver Serv, Madrid, Spain
关键词
PRIMARY SCLEROSING CHOLANGITIS; INFLAMMATORY-BOWEL-DISEASE; SIMPLIFIED CRITERIA; HEPATITIS; CHILDREN; VANCOMYCIN; BUDESONIDE; PREDNISONE; CHILDHOOD; DIAGNOSIS;
D O I
10.1016/j.clinre.2014.03.015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Autoimmune liver disease is the second commonest cause of chronic liver disease in teenagers. There are several forms including autoimmune hepatitis, autoimmune sclerosing cholangitis, primary sclerosing cholangitis and various overlap syndromes, classified on the basis of different serum antibody profiles, histological features and appearances on cholangiography. Treatment with immunosupressants is usually effective, but often required medium to long-term, raising concerns about side effects and adherence to therapy. For a minority of children presenting in acute liver failure or with difficult-to-treat disease liver transplantation is a possible option, although risk of recurrence in the grafted liver remains lifelong. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:273 / 276
页数:4
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