K. Dohmen et al., POST-INFANTILE GIANT-CELL HEPATITIS IN AN ELDERLY FEMALE-PATIENT WITHSYSTEMIC LUPUS-ERYTHEMATOSUS, Journal of gastroenterology, 29(3), 1994, pp. 362-368
A 69-year-old Japanese female was admitted because of general fatigue.
Laboratory data showed elevation of serum total bilirubin, transamina
se, gamma-glutamyl transpeptidase, and creatinine levels. An immunolog
ical study revealed hypergammaglobulinemia, low titer of complement, a
nd high titers of antinuclear antibody, anti-DNA antibody, and circula
ting immune complexes. Antibodies to parainfluenza virus 3 were positi
ve. Histology of the liver disclosed numerous giant cell hepatocyte tr
ansformations with the lobular architecture being slightly distorted b
y portal inflammation and fibrosis. These findings led us to make a di
agnosis of giant cell hepatitis associated with systemic lupus erythem
atosus. Prednisolone was effective in improving the anemia and the ser
um immunoglobulin, immune complex, and antinuclear antibody levels. Th
e addition of cyclosporine to the initial corticosteroid therapy was a
lso beneficial in decreasing the transaminase level and in improving l
iver histology. The patient died of acute pneumonitis and renal failur
e on the 166th day after admission. Parainfluenza virus 3 and autoimmu
ne mechanisms were thus considered to be the causes of the giant cell
hepatitis.