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非典型帕金森综合征:结构、功能及分子影像学特征

Atypical Parkinsonian Syndromes: Structural, Functional, and Molecular Imaging Features.

作者信息

Keir Graham, Roytman Michelle, Mashriqi Faizullah, Shahsavarani Shaya, Franceschi Ana M

机构信息

From the Neuroradiology Division (G.K., M.R.), Department of Radiology, Weill Cornell Medical College, NY-Presbyterian Hospital, New York, New York.

Neuroradiology Division (F.M., S.S., A.M.F.), Department of Radiology, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Lenox Hill Hospital, New York, New York.

出版信息

AJNR Am J Neuroradiol. 2024 Dec 9;45(12):1865-1877. doi: 10.3174/ajnr.A8313.

Abstract

Atypical parkinsonian syndromes, also known as Parkinson-plus syndromes, are a heterogeneous group of movement disorders, including dementia with Lewy bodies (DLB), progressive supranuclear palsy (PSP), multisystem atrophy (MSA), and corticobasal degeneration (CBD). This review highlights the characteristic structural, functional, and molecular imaging features of these complex disorders. DLB typically demonstrates parieto-occipital hypometabolism with involvement of the cuneus on FDG-PET, whereas dopaminergic imaging, such as [I]-FP-CIT SPECT (DaTscan) or fluorodopa (FDOPA)-PET, can be utilized as an adjunct for diagnosis. PSP typically shows midbrain atrophy on structural imaging, whereas FDG-PET may be useful to depict frontal lobe hypometabolism and tau-PET confirms underlying tauopathy. MSA typically demonstrates putaminal or cerebellar atrophy, whereas FDG-PET highlights characteristic nigrostriatal or olivopontocerebellar hypometabolism, respectively. Finally, CBD typically shows asymmetric atrophy in the superior parietal lobules and corpus callosum, whereas FDG and tau-PET demonstrate asymmetric hemispheric and subcortical involvement contralateral to the side of clinical deficits. Additional advanced neuroimaging modalities and techniques described may assist in the diagnostic work-up or are promising areas of emerging research.

摘要

非典型帕金森综合征,也称为帕金森叠加综合征,是一组异质性的运动障碍,包括路易体痴呆(DLB)、进行性核上性麻痹(PSP)、多系统萎缩(MSA)和皮质基底节变性(CBD)。本综述重点介绍了这些复杂疾病的特征性结构、功能和分子影像学特征。DLB在FDG-PET上通常表现为顶枕叶代谢减低,楔叶受累,而多巴胺能成像,如[I]-FP-CIT SPECT(DaTscan)或氟多巴(FDOPA)-PET,可作为诊断的辅助手段。PSP在结构成像上通常显示中脑萎缩,而FDG-PET可能有助于描绘额叶代谢减低,tau-PET可证实潜在的tau蛋白病。MSA通常表现为壳核或小脑萎缩,而FDG-PET分别突出显示特征性的黑质纹状体或橄榄脑桥小脑代谢减低。最后,CBD通常显示顶上小叶和胼胝体不对称萎缩,而FDG和tau-PET显示与临床缺陷侧相对的对侧半球和皮质下不对称受累。所描述的其他先进神经影像学方法和技术可能有助于诊断检查,或是新兴的有前景的研究领域。

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