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A rare case of neuro-Behçet’s disease presenting with limbic encephalitis

机译:神经性贝塞特病伴边缘性脑炎的罕见病例

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摘要

Behçet's syndrome is a recurrent systemic inflammation with an unknown etiology. The onset of the condition often occurs in the second decade of life and it is more common in males than in females. One of the most feared organ involvements associated with BS is neurological involvement, which often affects the brain stem, although hemispheric involvement may be primary in a limited number of patients. Parenchymal neurological involvement in BS affects the prognosis unfavorably, as it may result in severe sequelae or mortality. Early diagnosis and treatment is important to prevent sequelae. Herein, we report the first case of neuro-Behçet’s disease presenting with limbic encephalitis who received early stage immunotherapy.
机译:贝塞综合症是一种复发性全身性炎症,病因不明。这种病的发作通常发生在生命的第二个十年,男性多于女性。与BS相关的最令人担心的器官受累之一是神经受累,尽管半球受累可能是少数患者的主要病因,但神经受累通常会影响脑干。 BS的实质神经受累会对预后产生不利影响,因为它可能导致严重的后遗症或死亡。早期诊断和治疗对预防后遗症很重要。在此,我们报告了首例伴有边缘性脑炎的神经性贝塞特病,并接受了早期免疫治疗。

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