| Autor: |
Dohmen, Kazufumi, Ohtsuka, Shoji, Nakamura, Haruki, Arase, Koichi, Yokogawa, Yasushi, Asayama, Ryoukichi, Kuroiwa, Shigekazu, Ishibashi, Hiromi, Dohmen, K, Ohtsuka, S, Nakamura, H, Arase, K, Yokogawa, Y, Asayama, R, Kuroiwa, S, Ishibashi, H |
| Předmět: |
|
| Zdroj: |
Journal of Gastroenterology; Jun1994, Vol. 29 Issue 3, p362-368, 7p |
| Abstrakt: |
A 69-year-old Japanese female was admitted because of general fatigue. Laboratory data showed elevation of serum total bilirubin, transaminase, gamma-glutamyl transpeptidase, and creatinine levels. An immunological study revealed hypergammaglobulinemia, low titer of complement, and high titers of antinuclear antibody, anti-DNA antibody, and circulating immune complexes. Antibodies to parainfluenza virus 3 were positive. Histology of the liver disclosed numerous giant cell hepatocyte transformations with the lobular architecture being slightly distorted by portal inflammation and fibrosis. These findings led us to make a diagnosis of giant cell hepatitis associated with systemic lupus erythematosus. Prednisolone was effective in improving the anemia and the serum immunoglobulin, immune complex, and antinuclear antibody levels. The addition of cyclosporine to the initial corticosteroid therapy was also beneficial in decreasing the transaminase level and in improving liver histology. The patient died of acute pneumonitis and renal failure on the 166th day after admission. Parainfluenza virus 3 and autoimmune mechanisms were thus considered to be the causes of the giant cell hepatitis. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
|
Full text from SpringerLink