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抗 CASPR2 抗体相关脑炎伴嗅觉缺失和脱髓鞘假瘤:一例报告。

Anti-CASPR2 antibody associated encephalitis with anosmia and demyelinating pseudotumor: A case report.

机构信息

Department of Neurosurgery, West China Hospital of Sichuan University, Chengdu, Sichuan Province, PR China.

Department of Neurology, West China Hospital of Sichuan University, Chengdu, Sichuan Province, PR China.

出版信息

J Neuroimmunol. 2020 Nov 15;348:577393. doi: 10.1016/j.jneuroim.2020.577393. Epub 2020 Sep 12.

Abstract

A 20-year-old female presented with fine motor deficits and visual field defect was admitted to our hospital. CSF tests for autoimmune encephalitis antibodies and onconeuronal antibodies were unremarkable. MRI showed unilateral lesion involving left basal ganglia, external capsule, insula, hippocampus, and amygdala, which was considered to be demyelinating pseudotumor after surgical intervention. The patient's symptoms relieved so she didn't consent to immunotherapy. Two years and a half later our patient reported sudden anosmia. Reexamination by MRI demonstrated a new lesion. We then detected anti-CASPR2 antibodies in the patient's serum and gave her immunotherapy.

摘要

一位 20 岁女性因运动精细度缺陷和视野缺损就诊于我院。脑脊液自身免疫性脑炎抗体和神经元抗体检测无明显异常。磁共振成像显示左侧基底节、外囊、岛叶、海马和杏仁核单侧病变,术后考虑为脱髓鞘假瘤。患者症状缓解,因此不同意免疫治疗。两年半后,患者突然出现嗅觉丧失。再次磁共振成像显示新的病变。我们随后在患者血清中检测到抗 CASPR2 抗体,并给予免疫治疗。

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