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

dc.contributor.authorKeser, Melike
dc.contributor.authorSomer, Ayper
dc.contributor.authorKara, Buelent
dc.contributor.authorSalman, Nuran
dc.contributor.authorYalcin, Isik
dc.contributor.authorCan, Emrah
dc.date.accessioned2021-03-06T11:46:40Z
dc.date.available2021-03-06T11:46:40Z
dc.date.issued2006
dc.identifier.citationCan E., Kara B., Somer A., Keser M., Salman N., Yalcin I., "Neuro-Behcet disease presenting as secondary pseudotumor syndrome: Case report", EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, cilt.10, ss.97-99, 2006
dc.identifier.issn1090-3798
dc.identifier.otherav_f0ac5c9b-4976-45ab-a485-3c41db53677b
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/157931
dc.identifier.urihttps://doi.org/10.1016/j.ejpn.2006.02.003
dc.description.abstractBehcet'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.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleNeuro-Behcet disease presenting as secondary pseudotumor syndrome: Case report
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
dc.contributor.department, ,
dc.identifier.volume10
dc.identifier.issue2
dc.identifier.startpage97
dc.identifier.endpage99
dc.contributor.firstauthorID38602


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