Department of Radiology, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo, 173-8605, Japan.
Department of Physiology, School of Medicine, Keio University, Tokyo, Japan.
Neuroradiology. 2019 Nov;61(11):1333-1339. doi: 10.1007/s00234-019-02289-8. Epub 2019 Sep 13.
This short report clarifies the heterogeneity of structural magnetic resonance imaging (MRI) findings in seven demented patients due to pathologically accumulated TAR DNA-binding protein-43 (TDP-43) protein using visual analyses including visual rating scales (i.e., global cortical atrophy and medial temporal atrophy scales). In addition to the well-known frontotemporal lobar atrophy, structural MRI has revealed multifaceted imaging findings including asymmetric atrophy of the frontoparietal lobe and cerebral peduncle, midbrain atrophy, and localized or diffuse white matter T2 hyperintensity. Understanding of these multifaceted neuroimaging findings is important for the precise antemortem diagnosis of TDP-43 proteinopathy.
本短篇报告通过视觉分析(包括整体皮质萎缩和内侧颞叶萎缩量表等视觉评分量表)阐明了 7 例由于病理性聚集的 TAR DNA 结合蛋白-43(TDP-43)蛋白导致的痴呆患者结构磁共振成像(MRI)结果的异质性。除了众所周知的额颞叶萎缩外,结构 MRI 还揭示了多方面的影像学发现,包括额顶叶和大脑脚的不对称性萎缩、中脑萎缩以及局灶性或弥漫性白质 T2 高信号。理解这些多方面的神经影像学发现对于 TDP-43 蛋白病的精确生前诊断非常重要。