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非典型多系统萎缩是额颞叶变性的一种新亚型:与α-突触核蛋白相关的额颞叶变性。

Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein.

作者信息

Aoki Naoya, Boyer Philip J, Lund Cheryl, Lin Wen-Lang, Koga Shunsuke, Ross Owen A, Weiner Myron, Lipton Anne, Powers James M, White Charles L, Dickson Dennis W

机构信息

Department of Neuroscience, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL, 32224, USA.

出版信息

Acta Neuropathol. 2015 Jul;130(1):93-105. doi: 10.1007/s00401-015-1442-z. Epub 2015 May 12.

Abstract

Multiple system atrophy (MSA) is a sporadic neurodegenerative disease clinically characterized by cerebellar signs, parkinsonism, and autonomic dysfunction. Pathologically, MSA is an α-synucleinopathy affecting striatonigral and olivopontocerebellar systems, while neocortical and limbic involvement is usually minimal. In this study, we describe four patients with atypical MSA with clinical features consistent with frontotemporal dementia (FTD), including two with corticobasal syndrome, one with progressive non-fluent aphasia, and one with behavioral variant FTD. None had autonomic dysfunction. All had frontotemporal atrophy and severe limbic α-synuclein neuronal pathology. The neuronal inclusions were heterogeneous, but included Pick body-like inclusions. The latter were strongly associated with neuronal loss in the hippocampus and amygdala. Unlike typical Pick bodies, the neuronal inclusions were positive on Gallyas silver stain and negative on tau immunohistochemistry. In comparison to 34 typical MSA cases, atypical MSA had significantly more neuronal inclusions in anteromedial temporal lobe and limbic structures. While uncommon, our findings suggest that MSA may present clinically and pathologically as a frontotemporal lobar degeneration (FTLD). We suggest that this may represent a novel subtype of FTLD associated with α-synuclein (FTLD-synuclein).

摘要

多系统萎缩(MSA)是一种散发性神经退行性疾病,临床特征为小脑体征、帕金森综合征和自主神经功能障碍。病理上,MSA是一种α-突触核蛋白病,影响纹状体黑质和橄榄脑桥小脑系统,而新皮质和边缘系统受累通常较轻。在本研究中,我们描述了4例非典型MSA患者,其临床特征与额颞叶痴呆(FTD)一致,包括2例皮质基底节综合征患者、1例进行性非流利性失语患者和1例行为变异型FTD患者。所有患者均无自主神经功能障碍。所有患者均有额颞叶萎缩和严重的边缘系统α-突触核蛋白神经元病变。神经元包涵体具有异质性,但包括Pick小体样包涵体。后者与海马体和杏仁核中的神经元丢失密切相关。与典型的Pick小体不同,这些神经元包涵体在Gallyas银染色中呈阳性,在tau免疫组化中呈阴性。与34例典型MSA病例相比,非典型MSA在前内侧颞叶和边缘结构中的神经元包涵体明显更多。虽然不常见,但我们的研究结果表明,MSA在临床和病理上可能表现为额颞叶变性(FTLD)。我们认为,这可能代表了一种与α-突触核蛋白相关的新型FTLD亚型(FTLD-突触核蛋白)。

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