Division of Radiology, Department of Pathophysiological and Therapeutic Science, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
AJNR Am J Neuroradiol. 2009 Oct;30(9):1725-30. doi: 10.3174/ajnr.A1662. Epub 2009 Jun 18.
Cerebellar atrophy and white matter T2-hyperintensities have been characterized as cerebellar lesions of multiple system atrophy (MSA). The aim of the study was to correlate MR images with histologic findings in cerebellar lesions of MSA.
Postmortem T2-weighted images using 1.5T were compared with histologic findings in 7 postmortem-proved cases with MSA. The MR imaging findings in the cerebellar cortices and deep white matter dentate nucleus regions were compared with their histologic findings in each case.
We detected 3 types of cerebellar changes: type 1, no apparent atrophy or signal-intensity changes; type 2, cerebellar atrophy and inhomogeneous (patchy and/or confluent) cerebellar white matter hyperintensities; and type 3, cerebellar atrophy and diffuse white matter hyperintensities. Hypointensities were seen in the dentate nucleus regions. Atrophy of the cerebellar white matter was more severe than that of cerebellar cortices, and this anatomy was well depicted on coronal images. Histologically, degeneration was more severe in the cerebellar white matter than in the cerebellar cortices. Hyperintensities in the cerebellar white matter showed loss of myelinated fibers and gliosis. Hypointensities in the dentate nucleus regions revealed diffuse ferritin deposition in preserved dentate nuclei and white matter both around and within the nuclei.
Hyperintensities in the cerebellar white matter reflect degenerated white matter associated with loss of myelinated fibers and gliosis, whereas hypointensities in the dentate nucleus regions reflect diffuse ferritin deposition in preserved dentate nuclei and white matter around and within the nuclei. Degeneration is more severe in the cerebellar white matter than in the cerebellar cortices.
小脑萎缩和脑白质 T2 高信号已被确定为多系统萎缩(MSA)的小脑病变。本研究旨在将磁共振成像(MRI)与 MSA 小脑病变的组织学发现进行相关分析。
对 7 例经尸检证实的 MSA 患者的 T2 加权 MRI 图像进行了 1.5T 后处理,将其与组织学发现进行了对比。对小脑皮质和深部白质齿状核区域的 MRI 表现与每个病例的组织学发现进行了对比。
我们发现了 3 种小脑变化类型:1 型,无明显萎缩或信号强度改变;2 型,小脑萎缩和不均匀(斑片状和/或融合性)小脑白质高信号;3 型,小脑萎缩和弥漫性白质高信号。齿状核区域可见低信号。小脑白质萎缩比小脑皮质更严重,冠状位图像能很好地显示这种解剖结构。组织学上,小脑白质的退变比小脑皮质更严重。小脑白质的高信号提示脱髓鞘纤维和胶质增生。齿状核区域的低信号提示在保留的齿状核和核周围及核内的白质中弥漫性铁蛋白沉积。
小脑白质的高信号反映了与脱髓鞘纤维丢失和胶质增生相关的退变白质,而齿状核区域的低信号反映了在保留的齿状核和核周围及核内的白质中弥漫性铁蛋白沉积。小脑白质的退变比小脑皮质更严重。