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[进行性变性失语症:18例临床及神经放射学观察]

[Progressive degenerative aphasia: clinical and neuroradiological observations in 18 cases].

作者信息

Robles A, Vilariño I, Sesar A, Pardellas H, Cacabelos P, Noya M

机构信息

Servicio de Neurología, Hospital General de Galicia, Complejo Hospitalario Universitario de Santiago, Santiago de Compostela, La Coruña, España.

出版信息

Rev Neurol. 1997 Apr;25(140):505-12.

PMID:9172907
Abstract

INTRODUCTION

In some types of degenerative dementia aphasia is the main disorder. In primary progressive aphasia. (PPA) atrophy is limited to the dominant peri-sylvan region. We present 18 cases of progressive aphasia of degenerative origin, with or without dementia.

MATERIAL AND METHODS

We describe the clinical and neuro-radiological findings in 3 patients with 'aphasic dementia and motor neuron disease (ADMND)', 7 with 'semantic dementia' (DS), and 4 with 'fronto-temporal dementia' with 'marked non-fluent aphasia' (AFTD). Criteria published in recent years were used.

RESULTS

In patients with ADMND non-fluent aphasia progressed to global aphasia, with dementia occurring after 2-9 months, and death after an average of 17 months. In cases with SD, initial anomic aphasia progressed to transcortical sensory or global aphasia, and in patients with AFTD, Broca's aphasia or motor transcortical aphasia progressed to global aphasia. Seven of these patients had been initially diagnosed as having PPA and became demented after two years or more. In most of the cases the cognitive disorder had the characteristics of fronto-temporal dementia. All cases had cortical atrophy or asymmetrical cortical or cortico-subcortical atrophy. The 4 cases of non-fluent PPA were not demented after 21 months-6 years of illness, and showed perisylvan and left fronto-temporopolar atrophy.

CONCLUSIONS

The PPA may correspond to the initial form of at least three varieties of dementia, usually the fronto-temporal type. Dementia occurs after two years or more, except in patients with motor neurone disease, when there is a latent period of less than one year.

摘要

引言

在某些类型的退行性痴呆中,失语是主要病症。在原发性进行性失语(PPA)中,萎缩局限于优势半球的颞叶周围区域。我们报告了18例退行性病因导致的进行性失语病例,伴有或不伴有痴呆。

材料与方法

我们描述了3例“失语性痴呆与运动神经元病(ADMND)”、7例“语义性痴呆”(SD)和4例伴有“明显非流利性失语”的“额颞叶痴呆”(AFTD)患者的临床和神经放射学表现。采用了近年来发表的标准。

结果

ADMND患者的非流利性失语进展为完全性失语,2至9个月后出现痴呆,平均17个月后死亡。SD患者最初的命名性失语进展为经皮质感觉性或完全性失语,AFTD患者的布罗卡失语或运动性经皮质失语进展为完全性失语。其中7例患者最初被诊断为PPA,两年或更长时间后出现痴呆。在大多数病例中,认知障碍具有额颞叶痴呆的特征。所有病例均有皮质萎缩或不对称的皮质或皮质下皮质萎缩。4例非流利性PPA患者在患病21个月至6年后未出现痴呆,表现为颞叶周围和左侧额颞极萎缩。

结论

PPA可能对应至少三种痴呆类型的初始形式,通常为额颞叶型。除运动神经元病患者潜伏期少于一年外,痴呆在两年或更长时间后出现。

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