IgG4抗神经束蛋白155抗体阳性合并中枢和外周脱髓鞘综合征的视神经脱髓鞘。

IF 2.6 Q2 CLINICAL NEUROLOGY
Journal of Central Nervous System Disease Pub Date : 2021-12-06 eCollection Date: 2021-01-01 DOI:10.1177/11795735211039913
Alice Verghese, Dhayalan Krishnan, Yuen Kang Chia, Luis Querol, Fu Liong Hiew
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引用次数: 2

摘要

视神经脱髓鞘是中枢性和外周性联合脱髓鞘(CCPD)的临床特征之一,具有异质的免疫发病机制和临床特征,与多发性硬化症(MS)和慢性炎症性脱髓鞘性多神经病变(CIDP)重叠。有趣的是,在发现抗副神经节蛋白神经束蛋白155(抗nf 155)抗体之前,对CIDP患者的早期研究也报道了视神经功能障碍。我们的目的是评估抗nf - 155 CIDP患者的视神经脱髓鞘。我们使用视觉诱发电位(VEP)和光学相干断层扫描(OCT)对2例抗nf - 155型CIDP患者进行了研究。两例患者均为远端获得性脱髓鞘对称(DADS)亚型CIDP。其他共同特征有明显的感觉共济失调、手部震颤、脑脊液蛋白显著升高、抗nf - 155抗体高滴度、对皮质类固醇和静脉注射免疫球蛋白(IVIg)反应差。未发现中枢神经系统神经影像学异常。两例患者视力和色觉正常,但1例有亚临床右侧相对传入瞳孔缺损(RAPD)。两例VEP均表现为双侧P100延迟延长。RAPD患者的OCT表现为中度至重度视网膜神经纤维层(RNFL)变薄。用抗nf - 155抗体在亚临床CIDP中鉴定视神经脱髓鞘,扩大了CCPD亚群中脱髓鞘的范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Optic Nerve Demyelination in IgG4 Anti-Neurofascin 155 Antibody-Positive Combined Central and Peripheral Demyelination Syndrome.

Optic Nerve Demyelination in IgG4 Anti-Neurofascin 155 Antibody-Positive Combined Central and Peripheral Demyelination Syndrome.

Optic Nerve Demyelination in IgG4 Anti-Neurofascin 155 Antibody-Positive Combined Central and Peripheral Demyelination Syndrome.

Optic Nerve Demyelination in IgG4 Anti-Neurofascin 155 Antibody-Positive Combined Central and Peripheral Demyelination Syndrome.

Optic nerve demyelination is one of the clinical features of combined central and peripheral demyelination (CCPD), an entity with heterogenous immunopathogenesis and clinical characteristics, overlapping between multiple sclerosis (MS) and chronic inflammatory demyelinating polyneuropathy (CIDP). Of interest, earlier studies among patients with CIDP prior to discovery of antibodies against paranodal protein neurofascin 155 (anti-NF 155) also reported optic nerve dysfunction. We aimed to evaluate optic nerve demyelination among anti-NF 155 CIDP patients. We studied 2 patients with anti-NF 155 CIDP using visual-evoked potentials (VEP) and optical coherence tomography (OCT). Both patients had distal acquired demyelinating symmetric (DADS) subtype CIDP. Other common features were prominent sensory ataxia, hand tremors, significantly elevated cerebral spinal fluid protein, high titre anti-NF 155 antibodies and poor response to corticosteroid and intravenous immunoglobulin (IVIg). No central nervous system neuroradiological abnormality detected. Both had normal visual acuity and colour vision, but one had subclinical right relative afferent pupillary defect (RAPD). VEP of both showed bilateral prolonged P100 latencies. OCT for patient with RAPD demonstrated moderate to severe retinal nerve fibre layer (RNFL) thinning. Identification of optic nerve demyelination among subclinical CIDP with anti-NF 155 antibodies expanded the spectrum of demyelination within the subset of CCPD.

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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
39
审稿时长
8 weeks
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