Kuba Hiroshi, Inamura Takanori, Ikezaki Kiyonobu, Inoha Satoshi, Nakamizo Akira, Shono Tadahisa, Fukui Kimiko, Fukui Masashi
Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, Japan.
J Clin Neurosci. 2002 Jan;9(1):33-6. doi: 10.1054/jocn.2001.1010.
Using criteria of the classification recently described by Nutt et al., we examined gait disorder in five patients with normal pressure hydrocephalus (NPH). Their cerebrospinal fluid (CSF) pressures were in the normal range, and trials of CSF removal produced temporary improvement of symptoms. Surgical procedures to relieve hydrocephalus improved gait disorders in all patients. No patient showed spasticity, sensory ataxia, cerebellar ataxia, extrapyramidal signs, or limb apraxia. All walked slowly with a wide base and a short stride. The arm swing normally associated with walking was preserved. In standing, patients were unsteady and fell easily when pushed. Four patients showed hesitation in initiating walking and in turning. These clinical features fit Nutt's criteria for frontal gait disorder and frontal disequilibrium. Unlike findings in Parkinson's disease, where similar gait disorders may occur, other extrapyramidal signs, Myerson's sign, and upper limb dysfunction were absent in NPH, and arm swing while walking was preserved. We suspect that ventricular dilatation disturbs neuronal connections between the supplementary motor area and the globus pallidus in NPH patients.
使用Nutt等人最近描述的分类标准,我们检查了5例正常压力脑积水(NPH)患者的步态障碍。他们的脑脊液(CSF)压力在正常范围内,脑脊液引流试验使症状暂时改善。缓解脑积水的外科手术改善了所有患者的步态障碍。没有患者出现痉挛、感觉性共济失调、小脑性共济失调、锥体外系体征或肢体失用症。所有人行走缓慢,步基宽且步幅短。通常与行走相关的摆臂动作得以保留。站立时,患者不稳定,推搡时容易跌倒。4例患者在开始行走和转弯时表现出迟疑。这些临床特征符合Nutt的额叶步态障碍和额叶平衡失调标准。与帕金森病中可能出现类似步态障碍的情况不同,NPH患者不存在其他锥体外系体征、迈尔森征和上肢功能障碍,且行走时摆臂动作得以保留。我们怀疑脑室扩张扰乱了NPH患者辅助运动区与苍白球之间的神经元连接。