Fibrosing cholestatic hepatitis is a well-described syndrome in patien
ts with immunodeficiency and chronic hepatitis B. It is clinically, bi
ologically, and histologically characterized by rapidly progressive he
patic failure, a mildly elevated serum aminotransferase level, an exte
nsive periportal fibrosis associated with intense cholestasis, mild in
flammatory cellular infiltrate, no cirrhosis, and a high hepatocellula
r level expression of B viral antigens. This syndrome reflected a dire
ct hepatocytopathic injury linked to high intrahepatic viral antigen e
xpression. Because the syndrome of fibrosing cholestatic hepatitis has
not been described in chronic hepatitis C, we report the first well-c
haracterized case in a renal transplant patient with chronic hepatitis
C and discuss the clinical and pathogenic implications of such a synd
rome in this setting.