Neuro-Behçet’s disease revealed by diencephalo-mesencephalic impairment

Jamal Aouifi, Houda Bouchama, Hajar Eljouadi, A. Hanine
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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.
间脑-中脑损伤所揭示的神经behaperet病
简介:behaperet病是一种病因不明的全身性变异性血管炎。神经系统受累被称为神经-白塞病(NBD),通常在出现神经系统症状和中枢神经系统影像学病变的患者中诊断出来。病例报告:一名42岁女性,有口腔生殖器溃疡史,表现为行为障碍和左半身重。脑磁共振成像(MRI)显示间脑-中脑区假性肿瘤伴T2和Flair高信号,弥散序列轻度高信号,未见造影剂摄取。结论:假性肿瘤性NBD是一种少见但严重的behet病表现。脑MRI是探索、检测和监测实质病变最有效的方法。
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