Les hépatopathies auto-immunes et leurs traitements [Auto-immune liver diseases and their treatment]


Autoria(s): Hess J.; Thorens J.; Pache I.; Troillet F.X.; Moradpour D.; Gonvers J.J.
Data(s)

2005

Resumo

There are three main types of auto-immune liver disease, auto-immune hepatitis, primary biliary cirrhosis and primary sclerosing cholangitis. In the case of auto-immune hepatitis, prednisone therapy, with or without azathioprine, can improve quality of life and halt progression to cirrhosis. If there is no response or if the therapy is poorly tolerated, mycophenolate mofetil or cyclosporin should be considered. Ursodeoxycholic acid (UDCA), at a dosage of 13 to 15 mg/kg/day slows the progression of fibrosis in patients with primary biliary cirrhosis. Pruritus may be treated with cholestyramine, rifampicin or opiate antagonists. Ursodeoxycholic acid at a dosage of 20 to 30 mg/kg/day will slow the evolution of fibrosis.

Identificador

http://serval.unil.ch/?id=serval:BIB_18701A1CC4D6

isbn:1660-9379

pmid:15770819

Idioma(s)

fr

Fonte

Revue médicale suisse, vol. 1, no. 3, pp. 242, 245-7

Palavras-Chave #Cholangitis; Hepatitis, Autoimmune; Humans; Immunosuppressive Agents; Liver Cirrhosis, Biliary
Tipo

info:eu-repo/semantics/review

article