Interferon (IFN) therapy has been used for the treatment of common diseases
such as hepatitis C, myeloproliferative disorders, autoimmune diseases and
various types of cancer. Given the biological properties of interferon, it
is not surprising that there are a larger number of side effects due to it
s use. Although rheumatoid arthritis (RA) is one of the most common autoimm
une diseases found in clinical practice, it does not seem to be frequently
related to IFN therapy. We report a 40-year-old female patient who, after h
igh doses of IFN-alpha therapy for malignant melanoma, developed symmetrica
l polyarthritis, with pain and oedema in small and large joints, associated
with prolonged morning stiffness. She had positive rheumatoid factor and D
R4 HLA phenotype. She was treated with deflazacort (6 mg/day), chloroquine
and NSAIDs, with a partial response. In conclusion, although the developmen
t of RA after IFN therapy is a rare event, IFN may work as a 'trigger' for
such complication, leading to deregulation in the immune cascade in a perso
n genetically predisposed.