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经病理证实的伴或不伴运动神经元变性的额颞叶痴呆(FTLD)的萎缩模式。

Patterns of atrophy in pathologically confirmed FTLD with and without motor neuron degeneration.

作者信息

Whitwell Jennifer L, Jack Clifford R, Senjem Matthew L, Josephs Keith A

机构信息

Department of Radiology, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Neurology. 2006 Jan 10;66(1):102-4. doi: 10.1212/01.wnl.0000191395.69438.12.

DOI:10.1212/01.wnl.0000191395.69438.12
PMID:16401855
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2752419/
Abstract

The authors used voxel-based morphometry to compare the patterns of brain atrophy in two variants of pathologically confirmed frontotemporal lobar degeneration (FTLD): FTLD with motor neuron disease (FTLD-MND) and FTLD with ubiquitin-only-immunoreactive neuronal changes (FTLD-U). Patterns of atrophy were distinct and different from each other. A localized pattern of frontal lobe atrophy was found in FTLD-MND with a more widespread pattern of atrophy affecting the frontal and temporal lobes in FTLD-U.

摘要

作者使用基于体素的形态测量法,比较了两种经病理证实的额颞叶痴呆(FTLD)变体中的脑萎缩模式:伴运动神经元病的额颞叶痴呆(FTLD-MND)和仅具有泛素免疫反应性神经元变化的额颞叶痴呆(FTLD-U)。萎缩模式彼此不同且有明显差异。在FTLD-MND中发现额叶局限性萎缩模式,而在FTLD-U中则有更广泛的萎缩模式,累及额叶和颞叶。