Central nervous system (CNS) complications are rarely reported in either ju
venile or adult onset inflammatory myositides, such as dermatomyositis and
polymyositis. We report two children, aged 4 and 10 yr respectively, with a
diagnosis of juvenile dermatomyositis, both of whom subsequently developed
clinical features of severe CNS involvement. possibly consistent with cere
bral vasculopathy. One child died from apparent brainstem involvement; the
other developed seizures, pseudoseizures and clinical depression which resp
onded to aggressive immunosuppression. Although the vasculopathy or vasculi
tis underlying this disorder is known to have a systemic distribution, CNS
involvement has rarely been reported and may be under-recognized.