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夏科-马里-图斯病的感觉功能分析。

Analysis of sensory function in Charcot-Marie-Tooth disease.

作者信息

Ericson U, Borg K

机构信息

Department of Neurology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Acta Neurol Scand. 1999 May;99(5):291-6. doi: 10.1111/j.1600-0404.1999.tb00678.x.

Abstract

Ten patients each with Charcot-Marie-Tooth disease type 1 (CMT1), demyelinating form, and CMT2, axonal form, were subjected to analysis of sensory function including sensory screening and quantitative determination of thermal, thermal pain and vibratory thresholds in hands and feet. The threshold values were compared with data from age- and sex-matched control groups. All patients had a symmetrical sensory dysfunction, which was most prominent in the lower extremities. Temperature was the modality most often affected on screening and on quantitative determination of thresholds in both CMT1 and CMT2 patients. Mean thermal thresholds were significantly increased in both hands and feet in CMT1 as well as in CMT2 patients when compared with controls. There was no statistically significant difference between thermal thresholds in the CMT1 and CMT2 patients. Mean thermal pain thresholds were significantly increased in the feet of the CMT2 patients when compared with the controls and they were significantly higher in the hands of the CMT2 than in the CMT1 patients. Vibratory thresholds (VT) were abnormal in all CMT1 patients and in a majority of the CMT2 patients. Mean VT was significantly increased in hands and feet of both CMT1 and CMT2 patients when compared with the controls and the mean VT was significantly higher in the feet of the CMT1 than in the CMT2 patients. The difference with an increased heat pain threshold in the CMT2 patients and an increased VT in the CMT1 patients is suggested to be due to demyelination in CMT1 leading to affection of sensory function mediated by myelinated nerve fibres and to axonal disturbance in CMT2 with affection of sensory function mediated by small diameter myelinated and unmyelinated C-fibres.

摘要

分别选取了10例1型遗传性运动感觉神经病(CMT1,脱髓鞘型)和10例2型遗传性运动感觉神经病(CMT2,轴索性)患者,对其感觉功能进行分析,包括感觉筛查以及对手和足部的温度觉、热痛觉和振动觉阈值进行定量测定。将这些阈值与年龄和性别匹配的对照组数据进行比较。所有患者均存在对称性感觉功能障碍,在下肢最为明显。在CMT1和CMT2患者的筛查以及阈值定量测定中,温度觉是最常受影响的感觉模式。与对照组相比,CMT1和CMT2患者的手部和足部平均温度觉阈值均显著升高。CMT1和CMT2患者的温度觉阈值之间无统计学显著差异。与对照组相比,CMT2患者足部的平均热痛觉阈值显著升高,且CMT2患者手部的平均热痛觉阈值显著高于CMT1患者。所有CMT1患者以及大多数CMT2患者的振动觉阈值(VT)均异常。与对照组相比,CMT1和CMT2患者手部和足部的平均VT均显著升高,且CMT1患者足部的平均VT显著高于CMT2患者。CMT2患者热痛觉阈值升高与CMT1患者VT升高的差异被认为是由于CMT1中的脱髓鞘导致由有髓神经纤维介导的感觉功能受到影响,以及CMT2中的轴索紊乱导致由小直径有髓和无髓C纤维介导的感觉功能受到影响。

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