Kanzo
Online ISSN : 1881-3593
Print ISSN : 0451-4203
ISSN-L : 0451-4203
Clinical and pathological observations of HBs Ag carriers
Development of hepatic changes in HBs Ag carriers related to familial occurrence
Masaji NAMBUHiroshi UEYAMAYasumitsu IMAIIsho WADARyuichi SAKITAAyako MORIKAWAKoshi SAKUMAYutaka MAEDATadashi TAKAHARATadashi MAYUMIFumio TSUDAToshihiko NAMIHISAHideo UEDA
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1982 Volume 23 Issue 4 Pages 372-378

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Abstract
Clinical and pathological observations were performed in 246 subjects with persistent positive serum HBs Ag. They were divided into 3 groups, A: asymptomatic HBs Ag carrier (116 cases), B: HBs Ag carrier with abnormal liver function, firstly observed after long term follow-up study (52 cases), C: HBs Ag carrier with abnormal liver function during long term follow-up study (78 cases). Liver biopsies were performed in 66 cases of these carriers. HBV markers in their families were investigated in 97 subjects among 42 families.
In group A 5 biopsied cases showed minimal histologic change in all, in group B 3 cases showed liver cirrhosis (LC) in 18 cases, and in group C 12 showed LC and 7 showed hepatocellular carcinoma (HCC) in 43 biopsied cases.
Familial occurrence of HBs Ag carrier was significantly low in group A than in group B and C. Five cases with LC and HCC were histologically observed in 11 cases with familial occurrence, and one case showed LC in 19 cases without familial clustering.
Seventeen cases were biopsied twice during 9 years. Histological development were observed in 4 of 5 cases with familial occurrence and 6 of 12 without familial occurrence.
From these results it was suggested that a genetic background was related to the development of liver changes in HBs Ag carriers.
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© The Japan Society of Hepatology
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