Neuro-Behcet disease presenting as secondary pseudotumor syndrome: Case report

Behcet's disease is a multisystemic, recurrent, inflammatory disorder, which has a three-symptom complex comprising uveitis, oral aphtae and genital ulcerations. It is rare in childhood. The prevalence of neurologic involvement in BID is range of 10-49%, and shows a wide spectrum from isolated headache to subacute encephalopathy and severe psychosis. We report a 12-year-old Behcet's disease patient with secondary pseudotumor syndrome due to cerebral vein thrombosis and aim to review the literature. (C) 2006 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved