头痛是人类慢性坏死性肉芽肿性脑膜脑炎的最初表现:一个罕见的病例报告

Khaled Gharaibeh, Mustafa Al-Chalabi, Sohaib Lateef, Ajaz Sheikh
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引用次数: 0

摘要

慢性坏死性肉芽肿性脑膜脑炎是一种特发性炎症性疾病,可能有自身免疫介导的延迟型超敏反应。它通常会影响狗的中枢神经系统,在极少数情况下也会影响猫。然而,这种炎症性疾病很少在人类中报道。一名69岁女性,表现为亚急性间歇性剧烈头痛。脑MRI显示幕上及幕下实质多灶性强化病变及水肿及多灶性信号异常。脑脊液显示开口压升高,细胞增多,蛋白升高。MRA头,MRV头,脑血管造影,广泛的血清和脑脊液检查的感染性和自身免疫性病因也不显著。脑活检显示坏死性肉芽肿性炎症伴营养不良钙化。大剂量甲基强的松龙治疗后6周逐渐减少强的松治疗,头痛和脑部MRI异常得以缓解。本病例显示人类坏死性肉芽肿性脑膜脑炎对类固醇的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Headache as initial presentation of human chronic necrotizing granulomatous meningoencephalitis: A rare case report

Chronic necrotizing granulomatous meningoencephalitis is an idiopathic inflammatory disease with possible autoimmune mediated delayed type hypersensitivity response. It commonly affects the central nervous system of dogs, and on rare occasions cats. However, this inflammatory disease has rarely been reported in humans. A 69-year-old woman presented with subacute intermittent sharp headaches. Brain MRI revealed multifocal enhancing lesions and edema as well as multifocal signal abnormality throughout the supratentorial and infratentorial parenchyma. Cerebrospinal fluid showed elevated opening pressure, pleocytosis, and elevated protein. MRA head, MRV head, cerebral angiogram, extensive serum and CSF work up for infectious and autoimmune etiologies were also unremarkable. Brain biopsy revealed necrotizing granulomatous inflammation with dystrophic calcification. High dose of methylprednisolone followed by a 6-week prednisone taper resolved her headache and the brain MRI abnormalities. This case demonstrates the response of necrotizing granulomatous meningoencephalitis in humans to steroids.

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来源期刊
Brain disorders (Amsterdam, Netherlands)
Brain disorders (Amsterdam, Netherlands) Neurology, Clinical Neurology
CiteScore
1.90
自引率
0.00%
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0
审稿时长
51 days
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