S. Padeh et Jh. Passwell, SYSTEMIC LUPUS-ERYTHEMATOSUS PRESENTING AS IDIOPATHIC INTRACRANIAL HYPERTENSION, Journal of rheumatology, 23(7), 1996, pp. 1266-1268
We describe a 13-year-old girl who presented with an acute febrile dis
ease accompanied by headache, dizziness, nausea, decreased visual acui
ty, and diplopia. Examination showed papilledema, enlarged blind spots
, and visual field defects with an otherwise normal neurological exami
nation. The diagnosis of idiopathic intracranial hypertension was conf
irmed by increased intracranial pressure (cerebrospinal pressure >200
mm water) in the absence of any abnormal radiological findings of the
brain. Initially, only positive serology tests showing elevated titers
of anti-DNA antibodies and positive tests for anti-Sm and anti-RNP an
tibodies were found; however, 6 mo later clinical and laboratory findi
ngs were compatible with systemic lupus erythematosus (SLE). Our patie
nt illustrates that the possibility of SLE needs to be considered in t
he differential diagnosis of idiopathic intracranial hypertension.