Hepatitis C virus is not cleared after primary infection in 50-85% of subjects exposed to hepatitis C virus. Anti-viral treatment during the early phase of infection significantly enhances the likelihood of a sustained clearance of hepatitis C virus. Although, a variety of autoimmune-related side effects have been observed during interferon therapy for chronic hepatitis, immuno-mediated adverse reactions have not been reported during treatment of acute hepatitis C. We describe the case of a patient who developed acute hepatitis C virus infection and, while receiving pegylated interferon alpha-2b monotherapy, developed a severe polymyositis. This case illustrates the potential risk of autoimmunity by interferon, also for acute hepatitis, and underlines the importance of a prompt diagnosis and a rapid discontinuation of interferon treatment for an improvement of clinical outcomes. © 2005 Editrice Gastroenterologica Italiana S.r.l.
Venezia, G., Licata, A., Di Marco, V., Craxì, A., Almasio, P. (2005). Acute polymyositis during treatment of acute hepatitis C with pegylated interferon alpha-2b. DIGESTIVE AND LIVER DISEASE, 37(11), 882-885 [10.1016/j.dld.2005.06.010].
Acute polymyositis during treatment of acute hepatitis C with pegylated interferon alpha-2b
LICATA, Anna;Di Marco, V.;CRAXI, Antonio;ALMASIO, Pier Luigi
2005-01-01
Abstract
Hepatitis C virus is not cleared after primary infection in 50-85% of subjects exposed to hepatitis C virus. Anti-viral treatment during the early phase of infection significantly enhances the likelihood of a sustained clearance of hepatitis C virus. Although, a variety of autoimmune-related side effects have been observed during interferon therapy for chronic hepatitis, immuno-mediated adverse reactions have not been reported during treatment of acute hepatitis C. We describe the case of a patient who developed acute hepatitis C virus infection and, while receiving pegylated interferon alpha-2b monotherapy, developed a severe polymyositis. This case illustrates the potential risk of autoimmunity by interferon, also for acute hepatitis, and underlines the importance of a prompt diagnosis and a rapid discontinuation of interferon treatment for an improvement of clinical outcomes. © 2005 Editrice Gastroenterologica Italiana S.r.l.File | Dimensione | Formato | |
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