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Acute cerebellar ataxia of a patient with SLE
M Yaginuma1, M Suenaga, Y Shiono
1Department of Internal Medicine, Tokyo Metropolitan Bokutoh General Hospital, 4-23-15 Koutou-bashi, Sumida-ku, Tokyo, Japan.
Abstract:
We described a 28-year-old woman with systemic lupus erythematosus (SLE) presented with digestive tract, skin and renal symptoms and afterwards developed acute cerebellar ataxia, a paresis of the right inferior rectus muscle, left abducens paralysis and left facial palsy which seemed to be consistent with a brainstem lesion visible on magnetic resonance imaging (MRI). This lesion disappeared within 9 days of corticosteroid treatment. It is suggested that this lesion is focal edema induced by acute changes in the blood brain barrier secondary to a vasculopathy. Other causes, including local infarction, are unlikely.