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[神经退行性疾病的磁共振成像诊断]

[MRI diagnosis of neurodegenerative disorders].

作者信息

Iwata Makoto

机构信息

Department of Neurology, Tokyo Women's Medical University.

出版信息

Rinsho Shinkeigaku. 2005 Nov;45(11):947-51.

Abstract

Routine use of high field MRI has greatly contributed to the clinical diagnosis of neurodegenerative disorders, because MRI enables to visualize degenerative process showing either atrophy of the specific areas or degeneration of specific structures. Among many specific MRI signs which have been hitherto proposed to be diagnostic for certain neurodegenerative disorders, the author discussed here some clinically useful ones with neuropathological interpretations. "Humming-bird sign" is highly diagnostic for progressive supranuclear palsy (PSP) because it represents focal atrophy of the rostro-dorsal portion of mid-brain tegmentum where the neural centers for vertical gaze specifically affected in PSP are located. Un-treated Wilson disease patients show frequently "face of giant panda sign" of mid-brain which disappears after successful treatment. Although the sign is pathognomonic for Wilson disease, neuropathological entity of this MRI abnormality has not been known yet. MRI enables to discriminate two types of cerebellar atrophies; cerebellipetal atrophy in which ponto-, spino- and olivo-cerebellar fibers are lost, and cerebellofugal atrophy in which loss of Purkinje cells is the main pathological process. In cerebellipetal atrophy, cerebellar white matter shows T2 high signal due to the degeneration of nerve fibers in it but T2 low signal of dentate nucleus is usually well preserved. This combination of degenerative process realized" black teeth sign" of dentate nucleus in MRI. On the other hand, cerbellofugal atrophy shows "white teeth sign" of dentate nucleus, because the loss of Purkinje cell axons causes signal change of dentate nucleus where the axons of Purkinje cells are concentrating. "White teeth sign" could also be observed in case of the degeneration of dentate nucleus itself, like in DRPLA, but differential diagnosis between Purkinje cell loss and dentate degeneration is not so difficult, because the atrophy of the superior cerebellar peduncle is detectable in the latter but never seen in the former condition.

摘要

高场强MRI的常规应用极大地推动了神经退行性疾病的临床诊断,因为MRI能够显示退行性病变过程,表现为特定区域的萎缩或特定结构的变性。在众多迄今已被提出用于某些神经退行性疾病诊断的特定MRI征象中,作者在此讨论了一些具有临床实用性且能进行神经病理学解释的征象。“蜂鸟征”对进行性核上性麻痹(PSP)具有高度诊断价值,因为它代表中脑被盖部嘴侧背侧部分的局灶性萎缩,而PSP中垂直凝视的神经中枢就位于此处且受到特异性影响。未经治疗的肝豆状核变性患者常出现中脑的“大熊猫脸征”,成功治疗后该征象消失。尽管该征象对肝豆状核变性具有特异性,但这种MRI异常的神经病理学本质尚不清楚。MRI能够区分两种类型的小脑萎缩:向心性小脑萎缩,即桥脑、脊髓和橄榄小脑纤维缺失;离心性小脑萎缩,其中浦肯野细胞丢失是主要病理过程。在向心性小脑萎缩中,小脑白质因其中神经纤维变性而呈T2高信号,但齿状核的T2低信号通常保存完好。这种退行性过程的组合在MRI上表现为齿状核的“黑齿征”。另一方面,离心性小脑萎缩表现为齿状核的“白齿征”,因为浦肯野细胞轴突的丢失导致齿状核信号改变,而浦肯野细胞轴突在此处聚集。“白齿征”在齿状核本身变性的情况下也可观察到,如在齿状核红核苍白球路易体萎缩症(DRPLA)中,但浦肯野细胞丢失和齿状核变性之间的鉴别诊断并不困难,因为在后一种情况下可检测到小脑上脚萎缩,而在前一种情况中则从未见过。

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