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经尸检证实患有皮质基底节变性且以视空间构建障碍为首发症状的患者:先进的MRI序列如何助力临床实践。

Autopsy-proven patient with corticobasal degeneration presenting with visuo-constructive disorders as initial symptoms: How advanced MRI sequences can help clinical practice.

作者信息

Salman Yasmine, Huyghe Lara, Quenon Lisa, Ghysens Olivia, Malotaux Vincent, Tomé Sandra O, Thal Dietmar Rudolf, Hanseeuw Bernard J

机构信息

Institute of Neuroscience, UCLouvain, Brussels, Belgium.

Neurology Department, Saint-Luc University Hospital, Brussels, Belgium.

出版信息

J Alzheimers Dis. 2025 Mar;104(1):158-172. doi: 10.1177/13872877251314199. Epub 2025 Feb 17.

Abstract

BackgroundCortico-basal degeneration (CBD) is a neurodegenerative disease typically responsible for cortico-basal syndrome (CBS) or progressive limb apraxia. Half of CBD patients, however, present atypical symptoms, making the diagnosis difficult.ObjectiveWe reported the case of a woman in her late sixties (BM208), an unusual case of autopsy-proven CBD, showing early signs of Benson's syndrome or posterior cortical atrophy. In addition, we compared cognitive performance and atrophy in different brain regions of BM208 with other neurodegenerative diseases patients to highlight clinical signs that could have guided the diagnosis earlier.MethodsWe retrospectively compared BM208 to patients with typical amnestic Alzheimer's disease (AD) (n = 18, Mini-Mental State Exam (MMSE) scores between 18 and 24), Benson's syndrome due to AD (n = 3), CBS/progressive supranuclear palsy (PSP) syndrome (n = 5), and Lewy body dementia (LBD) patients (n = 3) and a control group (n = 24). All these participants underwent an MMSE, a complete neuropsychological examination and 3DT1 MRI.ResultsAlthough BM208 was more severely cognitively impaired overall, her cognitive performance was more similar to Benson's syndrome patients' cognitive profile compared to CBS patients or any other degenerative pathology (typical AD/LBD). Consistently, although BM208 was more atrophic than all other groups, she showed cortical atrophy that matched a Benson's syndrome pattern more than typical AD or CBS. However, the analysis of subcortical atrophy revealed atrophy of the basal ganglia corresponding CBS cases. Furthermore, visual analyses on sagittal T1 images showed atrophy of the midbrain, characteristic of CBS/PSP syndrome.ConclusionsThese results highlight the additive value of fine-grained MRI subcortical quantification to diagnose non-AD rare neurodegenerative disorders.

摘要

背景

皮质基底节变性(CBD)是一种神经退行性疾病,通常导致皮质基底节综合征(CBS)或进行性肢体失用症。然而,一半的CBD患者表现出非典型症状,这使得诊断变得困难。

目的

我们报告了一名60多岁女性(BM208)的病例,这是一例经尸检证实的不寻常的CBD病例,显示出本森综合征或后部皮质萎缩的早期迹象。此外,我们将BM208不同脑区的认知表现和萎缩情况与其他神经退行性疾病患者进行比较,以突出可能更早指导诊断的临床体征。

方法

我们回顾性地将BM208与典型遗忘型阿尔茨海默病(AD)患者(n = 18,简易精神状态检查表(MMSE)评分在18至24之间)、由AD引起的本森综合征患者(n = 3)、CBS/进行性核上性麻痹(PSP)综合征患者(n = 5)、路易体痴呆(LBD)患者(n = 3)以及一个对照组(n = 24)进行比较。所有这些参与者都接受了MMSE检查、全面的神经心理学检查和3DT1磁共振成像。

结果

尽管BM208总体认知功能受损更严重,但与CBS患者或任何其他退行性病变(典型AD/LBD)相比,她的认知表现与本森综合征患者的认知特征更相似。同样,尽管BM208比所有其他组萎缩更严重,但她的皮质萎缩与本森综合征模式更匹配,而不是典型的AD或CBS。然而,对皮质下萎缩的分析显示基底节萎缩与CBS病例相符。此外,矢状面T1图像的视觉分析显示中脑萎缩,这是CBS/PSP综合征的特征。

结论

这些结果突出了细粒度MRI皮质下定量分析在诊断非AD罕见神经退行性疾病中的附加价值。

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