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极晚发性多发性硬化症快速进展并伴有帕金森病:病例报告。

Rapidly progressive course of very late onset multiple sclerosis presenting with Parkinsonism: case report.

机构信息

Department of Neurology, University Hospital Gustav Carus, Technische Universität Dresden, Germany.

出版信息

Mult Scler. 2011 Feb;17(2):245-9. doi: 10.1177/1352458510384306. Epub 2010 Oct 4.

Abstract

Multiple sclerosis mainly affects young adolescents, making late-onset multiple sclerosis a rarity and diagnostic challenge, particularly for cases after age 80 years. We present an 82-year-old patient with multiple sclerosis with very late onset. As well as spastic paraplegia, additional Parkinsonism secondary to demyelination in the basal ganglia was observed in this case. In most publications, spinal cord lesions were more common in late-onset multiple sclerosis which, in contrast, could not be found in our case. Despite different treatment strategies, rapid clinical deterioration and death after about 2 years of disease course occurred. Further discrimination in late-onset multiple sclerosis (50-70 years) and multiple sclerosis with very late onset (above 70 years) might be considered. Future trials to elucidate potential benefit of immunosuppressive (and neuroprotective) therapies in these age groups are mandatory.

摘要

多发性硬化症主要影响青少年,因此,发病年龄较晚的多发性硬化症较为罕见,诊断也极具挑战,尤其是 80 岁以后发病的病例。我们报告了一例非常晚发性多发性硬化症的 82 岁患者。除痉挛性截瘫外,本例还观察到继发于基底节脱髓鞘的帕金森病。在大多数文献中,晚发性多发性硬化症更常见于脊髓病变,但在我们的病例中却没有发现。尽管采取了不同的治疗策略,但在大约 2 年的病程后,患者的临床状况仍迅速恶化并死亡。因此,可能需要对晚发性多发性硬化症(50-70 岁)和非常晚发性多发性硬化症(70 岁以上)进行进一步区分。对于这些年龄段,有必要进行未来的临床试验,以阐明免疫抑制(和神经保护)疗法的潜在获益。

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