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Title: Neuro-Behçet disease presenting as secondary pseudotumor syndrome: case report. Author: Can E, Kara B, Somer A, Keser M, Salman N, Yalçin I. Journal: Eur J Paediatr Neurol; 2006 Mar; 10(2):97-9. PubMed ID: 16595183. Abstract: Behçet'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 BD 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 Behçet's disease patient with secondary pseudotumor syndrome due to cerebral vein thrombosis and aim to review the literature.[Abstract] [Full Text] [Related] [New Search]