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[纹状体黑质变性(SND)中壳核的症状性偏侧性与磁共振成像(MRI)]

[Symptomatic laterality and magnetic resonance imaging (MRI) of the putamen in striatonigral degeneration (SND)].

作者信息

Yanagihara C, Ichikawa K, Kageyama Y, Satou M, Hoshino M

机构信息

Department of Neurology, Hyogo Prefectral Amagasaki Hospital.

出版信息

Rinsho Shinkeigaku. 1994 Apr;34(4):326-30.

PMID:8026124
Abstract

Asymmetric onset of parkinsonism appears not uncommon in SND. This study quantitatively investigated anatomical asymmetry of the putamen using MRI in relation to symptomatic laterality. Our study comprises six patients with SND, two men and four women, ranging in age from 50 to 77. Duration of illness ranged from 1 to 4 years. The Yahr stage was IV in 3 patients and I, III, or V in the others. The diagnosis of SND was made on medical history, neurological examination and MRI. All patients had asymmetric onset of parkinsonism. They subsequently had variable cerebellar ataxia and/or autonomic failure. All of them responded poorly to L-dopa therapy. MRI revealed the pontine and cerebellar atrophy and abnormalities of the putamen in most of the patients. MRI was performed using a 1.5 Tesla in 5 patients and 0.5 Tesla in one. Inversion Recovery (IR) image were utilized as T1-weighted images and proved optimal in showing anatomic detail. Spin-echo sequences were used to provide T2-weighted images. For measurement of the putaminal area and length in SND patients and 12 normal controls, we used two horizontal slices. One is passing through dorsal portion of the putamen, and the other through the ventral putamen. All the patients had the onset of hemi-parkinsonism and the symptoms progressed dominantly on the side of onset. With T1-weighted IR sequences, putaminal atrophy was demonstrated in all patients, more intense on the contralateral side to more symptomatic limbs. The anatomical asymmetry and the symptomatic laterality were less pronounced in advanced patients.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

帕金森综合征的不对称起病在进行性核上性麻痹(SND)中似乎并不少见。本研究使用磁共振成像(MRI)定量研究壳核的解剖不对称性及其与症状性偏侧的关系。我们的研究包括6例SND患者,2例男性和4例女性,年龄在50至77岁之间。病程为1至4年。3例患者处于Yahr分期IV期,其他患者处于I、III或V期。SND的诊断基于病史、神经学检查和MRI。所有患者均有帕金森综合征的不对称起病。随后他们出现了不同程度的小脑共济失调和/或自主神经功能衰竭。他们对左旋多巴治疗的反应均较差。MRI显示大多数患者存在脑桥和小脑萎缩以及壳核异常。5例患者使用1.5特斯拉的MRI进行检查,1例使用0.5特斯拉的MRI。反转恢复(IR)图像用作T1加权图像,在显示解剖细节方面效果最佳。自旋回波序列用于提供T2加权图像。为了测量SND患者和12名正常对照者的壳核面积和长度,我们使用了两个水平切片。一个穿过壳核的背侧部分,另一个穿过壳核的腹侧部分。所有患者均有偏侧帕金森综合征起病,且症状主要在起病侧进展。使用T1加权IR序列时,所有患者均显示壳核萎缩,在症状更明显肢体的对侧更为明显。在晚期患者中,解剖不对称性和症状性偏侧性不太明显。(摘要截断于250字)

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