Jamal Aouifi, Houda Bouchama, Hajar Eljouadi, A. Hanine
{"title":"Neuro-Behçet’s disease revealed by diencephalo-mesencephalic impairment","authors":"Jamal Aouifi, Houda Bouchama, Hajar Eljouadi, A. Hanine","doi":"10.5348/100021r02ja2022cr","DOIUrl":null,"url":null,"abstract":"\n Introduction: Behçet’s disease is a systemic variable vessel vasculitis with unknown cause. Neurologic involvement known as neuro-Behcet’s disease (NBD) is often diagnosed in patients who present neurological symptoms and radiological lesions of the central nervous system.\n\n Case Report: A 42-year-old woman with a history of orogenital ulceration presented with behavioral disorders and heaviness of left hemibody. Brain magnetic resonance imaging (MRI) was performed and showed a pseudo-tumor diencephalo-mesencephalic area with T2 and Flair hypersignal, a slight hypersignal in diffusion sequence, and no contrast uptake.\n\n Conclusion: Pseudotumoral NBD is a rare but severe manifestation of Behçet’s disease. Cerebral MRI is the most efficient method to explore, detect, and monitor parenchymal lesions.\n","PeriodicalId":269581,"journal":{"name":"Edorium Journal of Radiology","volume":"22 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Edorium Journal of Radiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5348/100021r02ja2022cr","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Behçet’s disease is a systemic variable vessel vasculitis with unknown cause. Neurologic involvement known as neuro-Behcet’s disease (NBD) is often diagnosed in patients who present neurological symptoms and radiological lesions of the central nervous system.
Case Report: A 42-year-old woman with a history of orogenital ulceration presented with behavioral disorders and heaviness of left hemibody. Brain magnetic resonance imaging (MRI) was performed and showed a pseudo-tumor diencephalo-mesencephalic area with T2 and Flair hypersignal, a slight hypersignal in diffusion sequence, and no contrast uptake.
Conclusion: Pseudotumoral NBD is a rare but severe manifestation of Behçet’s disease. Cerebral MRI is the most efficient method to explore, detect, and monitor parenchymal lesions.