Abstract
Multifocal progressive leukoencephalopathy, caused by reactivation of a latent JC-virus infection, has been classically correlated with certain conditions such as HIV infection, hematological malignancies and profound immunosuppression.
Nevertheless, more recently, rheumatic autoimmune diseases have been identified as a risk factor for the development of this condition. Amongst these diseases, Systemic Erythematous Lupus stands out as the disease with greater incidence for PM; a remarkable superior prevalence which doesn’t seem to be related with pharmacological immunosuppression, but with inherent characteristics of the disease
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