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进行性加重的MOG抗体相关性脑脊髓炎合并布氏杆菌病1例报道

A Case Report of Progressive Exacerbation of MOG Antibody-Associated Encephalomyelitis Complicated with Brucellosis
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摘要 髓鞘少突胶质细胞糖蛋白IgG相关疾病(MOGAD)是一种神经系统脱髓鞘疾病。MOGAD的典型症状为视神经炎(ON)、脊髓炎和急性播散性脑脊髓炎(ADEM)。目前MOG抗体相关性脑脊髓炎的治疗缺乏令人信服的前瞻性研究和随机对照研究的支持,其急性期的治疗方法主要是静脉注射甲泼尼龙、免疫球蛋白或血浆置换。我们在此报告1例进行性加重的MOG抗体相关性脑脊髓炎合并布氏杆菌病患者。 Myelin oligodendrocyte glycoprotein IgG-related disease (MOGAD) is a demyelinating disorder of the nervous system. Typical symptoms of MOGAD are optic neuritis (ON), myelitis, and acute disseminated encephalomyelitis (ADEM). At present, there is a lack of convincing prospective studies and randomized controlled studies for the treatment of MOG antibody-associated encephalomyelitis, and the treatment of the acute phase is mainly intravenous methylprednisolone, immunoglobulin, or plasma exchange. We report here one patient with progressive exacerbations of MOG antibody-associated encephalomyelitis complicated with brucellosis.
出处 《亚洲急诊医学病例研究》 2024年第3期59-63,共5页 Asian Case Reports in Emergency Medicine
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