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首页> 外文期刊>Arquivos de Neuro-Psiquiatria >Frontotemporal dementia with severe thalamic involvement: a clinical and neuropathological study
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Frontotemporal dementia with severe thalamic involvement: a clinical and neuropathological study

机译:前额颞叶痴呆伴重度丘脑受累:临床和神经病理学研究

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摘要

Frontotemporal dementia (FTD) is the third-leading cause of cortical dementia after Alzheimer's disease and Lewy body dementia, and is characterized by a dementia where behavioral disturbances are prominent and appear early in the course of the disease. We report the case of a 58 year-old man affected by dementia with behavioral disturbances, in addition to rigid-hypokinetic and a lower motor neuron syndrome that were present at later stages of the illness. Neuroimaging studies showed frontotemporal atrophy. Neuropathological studies revealed intense thalamic neuronal loss and astrocytic gliosis, as well as moderate frontotemporal neuronal loss, astrocytosis and spongiform degeneration. Thalamic degeneration has previously been described among the wide group of neuropathological features of FTD. The aim of the present study is to show the clinical and neuropathological aspects of thalamic degeneration in FTD, along with its role in behavioral disturbances, a common finding in this condition.
机译:额颞痴呆(FTD)是继阿尔茨海默氏病和路易氏体痴呆之后的第三大皮质痴呆病因,其特征是痴呆,其行为障碍在疾病过程中很明显并出现在疾病早期。我们报道了一例58岁的男性,除了在该病后期出现的刚性低运动和下运动神经元综合症外,还患有行为障碍性痴呆。神经影像学研究显示额颞萎缩。神经病理学研究显示,严重的丘脑神经元丢失和星形胶质细胞胶质增生,以及额颞中度神经元丢失,星形细胞增多和海绵状变性。先前已在众多FTD的神经病理学特征中描述了丘脑变性。本研究的目的是显示FTD中丘脑变性的临床和神经病理学方面,以及其在行为障碍中的作用,这是这种情况下的常见发现。

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