Arunodaya G R, Taly A B, Swamy H S
National Institute of Mental Health and Neuro Sciences (NIMHANS), Bangalore, India.
J Neurol Sci. 1995 May;130(1):35-8. doi: 10.1016/0022-510x(94)00271-o.
Sympathetic skin response (SSR) is a recently described objective method of studying sudomotor sympathetic nerve function and has been studied in a variety of peripheral neuropathies. We report SSR changes in nine patients with acute sensory ataxic neuropathy (ASAN). All had severe sensory and mild motor nerve conduction abnormalities; five had dysautonomia. SSR, elicited by electric shock and cough stimuli, was absent in three patients. Latency was normal in all when SSR was present. Two patients had SSR amplitude of 0.2 mV or less. Absence of SSR did not correlate with dysautonomia, absence of sensory nerve action potential or motor nerve conduction abnormalities. Follow up SSR studies revealed return of absent SSR in one patient over a period of 3 months, despite persistence of ataxia. To our knowledge, this is the first report of SSR changes in ASAN.
交感皮肤反应(SSR)是一种最近描述的研究汗腺运动交感神经功能的客观方法,已在多种周围神经病变中进行了研究。我们报告了9例急性感觉性共济失调性神经病(ASAN)患者的SSR变化。所有患者均有严重的感觉和轻度运动神经传导异常;5例有自主神经功能障碍。通过电击和咳嗽刺激诱发的SSR在3例患者中未引出。当SSR存在时,所有患者的潜伏期均正常。2例患者的SSR波幅为0.2mV或更低。SSR缺失与自主神经功能障碍、感觉神经动作电位缺失或运动神经传导异常无关。随访的SSR研究显示,1例患者在3个月内SSR缺失恢复,尽管共济失调持续存在。据我们所知,这是关于ASAN中SSR变化的首次报告。