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Copyright ©2008 The WJG Press and Baishideng.
World J Gastroenterol. Jun 7, 2008; 14(21): 3360-3367
Published online Jun 7, 2008. doi: 10.3748/wjg.14.3360
Table 1 Clinical, laboratory, and histological features at presentation of autoimmune hepatitis type 1, autoimmune hepatitis type 2, and autoimmune sclerosing cholangitis[120]
Type 1 AIHType 2 AIHASC
Median age in year11712
Females (%)757555
Mode of presentation (%)
Acute hepatitis474037
Acute liver failure3250
Insidious onset382537
Complication of chronic liver disease121026
Associated autoimmune diseases (%)222048
Inflammatory bowel disease (%)201244
Family history of autoimmune disease (%)434037
Abnormal cholangiogram (%)00100
ANA/SMA (%)1002596
Anti LKM1 (%)01004
pANCA (%)451174
Anti SLA (%)1585841
Increased IgG level (%)847589
Partial IgA deficiency (%)9455
Low C4 level (%)898370
Increased frequency of HLA DR*0301YesNo2No
Increased frequency of HLA DR*0701NoYesNo
Increased frequency of HLA DR*1301NoNoYes
Interface hepatitis (%)667235
Biliary features (%)28631
Cirrhosis (%)693815
Remission after immunosuppressive Treatment (%)978789
Table 2 Laboratory parameters at presentation in children with autoimmune hepatitis and autoimmune sclerosing cholangitis[20]
AIHASC
Bilirubin (nv < 20 micromol/L)35 (4-306)20 (4-179)
Albumin (nv > 35 g/L)35 (25-47)39 (27-54)
AST (nv < 50 IU/L)333 (24-4830)102 (18-1215)
INR (< 1.2)1.2 (0.96-2.5)1.1 (0.9-1.6)
GGT (nv < 50 IU/L)76 (29-383)129 (13-948)
AP (nv < 350 IU/L)356 (131-878)303 (104-1710)