Restuccia D, Mauguière F
Department of Clinical Neurophysiology, Hôpital Neurologique, Lyon, France.
Brain. 1991 Feb;114 ( Pt 1B):361-79. doi: 10.1093/brain/114.1.361.
Since the early study of Halliday and Wakefield (1963) it has generally been agreed that scalp somatosensory evoked potentials (SEPs) are normal in patients with dissociated loss of pain and temperature sensation. Up to now a few patients with abnormal spinal N13 and preserved scalp P14 and N20 have been reported in the literature, but there is no firm evidence, based on group data, that this dissociation can be related to any form of dissociated sensory loss. We studied median nerve SEPs in 24 patients with syringomyelia documented by CT scan or MRI. For the recording of the cervical N13 we used a Cv6 anterior cervical montage, which cancels the potentials generated above the foramen magnum and enhances the amplitude of N13. Scalp far-field and early cortical SEPs were recorded using a noncephalic reference electrode. Since N13 pathological changes are mainly changes in amplitude we measured the N13/P9 amplitude ratio in normal subjects and patients and found that it was a reliable index to quantify the amplitude decrease of N13. Absent or reduced N13 was observed in 40 median nerve SEPs (83%) in conjunction with normal P14 and N20 in 30 SEPs. Thus the dissociated loss of the cervical N13 was identified as the most conspicuous SEP feature in syringomyelia. A significant correlation was found between abnormal N13 and loss of pain and temperature sensations, whereas P14 abnormalities correlated well only with loss of joint and touch sensations. In the median nerve territory, sensation was either normal (6 cases) or lost only for pain and temperature (24 cases) when SEPs showed abnormal N13 and normal P14. Although it does not directly reflect the postsynaptic activity of spinal cells receiving their inputs from A delta and C fibres the N13 potential proved to be a reliable index of spinal cord grey matter dysfunction in syringomyelia.
自哈利迪和韦克菲尔德(1963年)早期研究以来,人们普遍认为,痛温觉分离性丧失的患者头皮体感诱发电位(SEP)正常。到目前为止,文献中已报道了少数脊髓N13异常而头皮P14和N20保留的患者,但基于群体数据,尚无确凿证据表明这种分离与任何形式的感觉分离性丧失有关。我们对24例经CT扫描或MRI证实患有脊髓空洞症的患者进行了正中神经SEP研究。为记录颈部N13,我们采用了Cv6颈前导联,该导联可消除枕骨大孔上方产生的电位并增强N13的波幅。使用非头部参考电极记录头皮远场和早期皮质SEP。由于N13的病理变化主要是波幅变化,我们测量了正常受试者和患者的N13/P9波幅比值,发现它是量化N13波幅降低的可靠指标。在40例正中神经SEP中观察到N13缺失或降低(83%),同时在30例SEP中P14和N20正常。因此,颈部N13的分离性丧失被确定为脊髓空洞症最显著的SEP特征。发现N13异常与痛温觉丧失之间存在显著相关性,而P14异常仅与关节和触觉丧失密切相关。在正中神经分布区域,当SEP显示N13异常而P14正常时,感觉要么正常(6例),要么仅痛温觉丧失(24例)。尽管N13电位不能直接反映从Aδ和C纤维接收输入的脊髓细胞的突触后活动,但它被证明是脊髓空洞症中脊髓灰质功能障碍的可靠指标。