中枢和周围神经系统联合脱髓鞘1例

Q Medicine
İ. Kılıç, C. Erdoğan, I. Aydin, F. Gökçay, A. Yüceyar
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引用次数: 0

摘要

合并中枢和周围神经系统脱髓鞘(CCPD)是一个相当新的概念,我们的知识仅限于几个病例系列和病例报告。我们的目的是用我们治疗慢性炎症性脱髓鞘性多神经根神经病变(CIDP)和多发性硬化症(MS)患者的经验来贡献文献。一个32岁的男性病人提出了神经性疾病的抱怨一年,最近开始视神经炎与中央脱髓鞘病变。临床、电生理和放射学反应在皮质类固醇治疗后达到,停止治疗后复发。他的第二次CCPD同时加重对静脉注射免疫球蛋白(IVIG)没有反应,但对静脉注射大剂量皮质类固醇有很好的反应。先前的研究报告了大多数CCPD患者对大剂量皮质类固醇和IVIG的反应不足。估计它是MS和CIDP之外的一种具有异质性特征的独特疾病。我们认为,对这种类固醇依赖状况的认识可能会提高我们在病理生理学和管理策略方面的知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combined central and peripheral nervous system demyelination: a case report
Combined central and peripheral nervous system demyelination (CCPD) is a fairly new concept and our knowledge is restricted to several case series and case reports. We aimed to contribute to the literature with our experiences in the management of a patient representing both chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) and multiple sclerosis (MS) features. A 32-year-male patient presented with neuropathic compaints for one year and recent onset of optic neuritis with central demyelinating lesions. Clinical, electrophysiological and radiological response was achieved with corticosteroid treatment and relapsed after cessation. His second simultaneous CCPD exacerbation did not respond on intravenous immunoglobulins (IVIG) but responded well on intravenous high dose corticosteroid. Previous studies reported inadequate responses to high-dose corticosteroids and IVIG in the majority of patients with CCPD. It's estimated to be a unique disease beyond MS and CIDP with heterogenous features. We suggest that awareness of this steroiddependent condition may improve our knowledge in the pathophysiology and management strategies.
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CiteScore
0.12
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4-8 weeks
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