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MOG 抗体相关性脱髓鞘疾病(MARD)中的 PRES 样表现。

PRES-like presentation in MOG antibody-related demyelination (MARD).

机构信息

Department of Neurology, Gold Coast University Hospital, Southport, QLD 4215, Australia.

Department of Radiology, Gold Coast University Hospital, Southport, QLD 4215, Australia.

出版信息

J Clin Neurosci. 2020 Feb;72:453-455. doi: 10.1016/j.jocn.2020.01.034. Epub 2020 Jan 22.

DOI:10.1016/j.jocn.2020.01.034
PMID:31982280
Abstract

A 33-year-old male presented with a progressive four-week history of frontal headache and left visual field impairment. MRI brain confirmed bilateral, asymmetric, occipital vasogenic oedema, suggestive of posterior reversible encephalopathy syndrome (PRES). Serum testing for MOG antibodies was positive, confirming a diagnosis of MOG antibody-related demyelination (MARD). A similar PRES-like pattern of white matter inflammation has been reported previously in neuromyelitis optica spectrum disorder but has not previously been reported in MARD.

摘要

一位 33 岁男性,表现为进行性四周的额头痛和左侧视野缺损。脑部 MRI 证实双侧、不对称、枕叶血管源性水肿,提示后部可逆性脑病综合征(PRES)。血清 MO G 抗体检测阳性,确诊为 MO G 抗体相关脱髓鞘疾病(MARD)。此前曾有报道称视神经脊髓炎谱系疾病存在类似 PRES 的脑白质炎症模式,但此前未在 MARD 中报道过。

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引用本文的文献

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Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Presenting as Intracranial Hypertension: A Case Report.髓鞘少突胶质细胞糖蛋白抗体相关性疾病表现为颅内压增高:病例报告。
Neurol Neuroimmunol Neuroinflamm. 2022 Oct 19;9(6). doi: 10.1212/NXI.0000000000200020. Print 2022 Nov.
2
Magnetic resonance imaging in neuromyelitis optica spectrum disorder.磁共振成像在视神经脊髓炎谱系疾病中的应用。
Clin Exp Immunol. 2021 Dec;206(3):251-265. doi: 10.1111/cei.13630. Epub 2021 Jul 6.