表现为非典型帕金森病的上运动神经元为主的运动神经元病:临床病理学研究。

IF 5.8 2区 医学 Q1 CLINICAL NEUROLOGY
Brain Pathology Pub Date : 2024-07-10 DOI:10.1111/bpa.13286
Aya Murakami, Shunsuke Koga, Shinsuke Fujioka, Adrianna E White, Kevin F Bieniek, Hiroaki Sekiya, Mariely DeJesus-Hernandez, NiCole A Finch, Marka van Blitterswijk, Masataka Nakamura, Yoshio Tsuboi, Melissa E Murray, Zbigniew K Wszolek, Dennis W Dickson
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引用次数: 0

摘要

肌萎缩侧索硬化症(ALS)是一种神经退行性疾病,以上下运动神经元症状为特征。然而,在有些病例中,上运动神经元(UMN)主要受累,导致临床表现为 UMN 主导型 ALS 或原发性侧索硬化症。此外,表现出以 UMN 为主导的运动神经元病(MND)模式并伴有皮质基底综合征(CBS)的病例也鲜有报道。本研究旨在阐明 UMN 显性 MND 患者的临床病理特征。我们回顾了 24 例伴有或不伴有额颞叶变性的 TDP-43 病变的 UMN 显性 MND 患者。此外,我们还查阅了病理确诊为皮质基底节变性(CBD)且最终临床诊断为CBS的患者(n = 10)和病理确诊为进行性核上麻痹(PSP)且最终临床诊断为PSP综合征的患者(n = 10)的病历。在24名以UMN为主的MND患者中,20人被临床诊断为非典型帕金森病,包括CBS(11人)和PSP综合征(8人)。只有两名患者在死前被诊断为运动神经元疾病。与CBD患者相比,以UMN为主的CBS MND患者较少表现出失语,他们也较少符合可能或疑似CBS的临床标准。同样,与患有 PSP 综合征的 PSP 患者相比,患有 PSP 综合征的 UMN 型 MND 患者较少符合可能患有 PSP 的临床标准。我们的研究结果表明,UMN为主的MND可模拟非典型帕金森病,在CBS和PSP综合征的鉴别诊断中应加以考虑,尤其是在不符合标准的情况下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Upper motor neuron-predominant motor neuron disease presenting as atypical parkinsonism: A clinicopathological study.

Upper motor neuron-predominant motor neuron disease presenting as atypical parkinsonism: A clinicopathological study.

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by upper and lower motor neuron signs. There are, however, cases where upper motor neurons (UMNs) are predominantly affected, leading to clinical presentations of UMN-dominant ALS or primary lateral sclerosis. Furthermore, cases exhibiting an UMN-predominant pattern of motor neuron disease (MND) presenting with corticobasal syndrome (CBS) have been sparsely reported. This study aims to clarify the clinicopathological features of patients with UMN-predominant MND. We reviewed 24 patients with UMN-predominant MND with TDP-43 pathology in the presence or absence of frontotemporal lobar degeneration. Additionally, we reviewed the medical records of patients with pathologically-confirmed corticobasal degeneration (CBD) who received a final clinical diagnosis of CBS (n = 10) and patients with pathologically-confirmed progressive supranuclear palsy (PSP) who received a final clinical diagnosis of PSP syndrome (n = 10). Of 24 UMN-predominant MND patients, 20 had a clinical diagnosis of an atypical parkinsonian disorder, including CBS (n = 11) and PSP syndrome (n = 8). Only two patients had antemortem diagnoses of motor neuron disease. UMN-predominant MND patients with CBS less frequently exhibited apraxia than those with CBD, and they were less likely to meet clinical criteria for possible or probable CBS. Similarly, UMN-predominant MND patients with PSP syndrome less often met clinical criteria for probable PSP than PSP patients with PSP syndrome. Our findings suggest that UMN-predominant MND can mimic atypical parkinsonism, and should be considered in the differential diagnosis of CBS and PSP syndrome, in particular when criteria are not met.

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来源期刊
Brain Pathology
Brain Pathology 医学-病理学
CiteScore
13.20
自引率
3.10%
发文量
90
审稿时长
6-12 weeks
期刊介绍: Brain Pathology is the journal of choice for biomedical scientists investigating diseases of the nervous system. The official journal of the International Society of Neuropathology, Brain Pathology is a peer-reviewed quarterly publication that includes original research, review articles and symposia focuses on the pathogenesis of neurological disease.
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