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血清阴性患者出现复发性同时中枢神经系统脱髓鞘病变伴可能的周围脱髓鞘病变/结节病。

Recurrent simultaneous central nervous system demyelination with possible peripheral demyelination / nodopathy in a seronegative patient.

机构信息

Department of Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

Department of Radiology, Hacettepe University Faculty of Medicine, Ankara, Turkey.

出版信息

Ideggyogy Sz. 2024 Sep 30;77(9-10):357-360. doi: 10.18071/isz.77.0357.

Abstract

Combined central and peripheral demyelination (CCPD) is a rare disease entity. Onset with the simultaneous central nervous system (CNS) and peripheral nervous system (PNS) involvement and its recurrence are exceptional. Anti-neurofascin antibodies have been shown to be present in up to 70% of cases, yet seronegative patients also exist. We present a case of seronegative recurrent CCPD. The PNS involvement was compatible with two episodes of recurrent Guillain-Barre syndrome (GBS), whereas the CNS involvement pattern was not typical for either multiple sclerosis (MS) or acute disseminated encephalomyelitis. The prognosis was excellent with pulse methylprednisolone, intravenous immunoglobulin, and plasmapheresis. This case highlights the varied clinical presentations of CCPD, extending beyond the realms of MS and chronic inflammatory demyelinating polyneuropathy, and underscores the potential for relapse. Importantly, to the best of our knowledge, this represents the inaugural instance of CCPD featuring PNS involvement in the form of recurrent GBS.

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摘要

联合中枢和周围脱髓鞘病变(CCPD)是一种罕见的疾病实体。同时出现中枢神经系统(CNS)和周围神经系统(PNS)受累并反复发作的情况极为罕见。高达 70%的病例中存在抗神经束蛋白抗体,但也存在血清阴性患者。我们报告了一例血清阴性复发性 CCPD。PNS 受累与两次复发性吉兰-巴雷综合征(GBS)一致,而 CNS 受累模式既不符合多发性硬化症(MS)也不符合急性播散性脑脊髓炎。脉冲甲基强的松龙、静脉注射免疫球蛋白和血浆置换的预后极好。该病例突出了 CCPD 的多种临床表现,不仅限于 MS 和慢性炎症性脱髓鞘性多发性神经病,还强调了复发的可能性。重要的是,据我们所知,这是首例以复发性 GBS 为表现形式的 PNS 参与 CCPD 的病例。

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