Chroni E, Hall S M, Hughes R A
Department of Neurology, United Medical School, Guy's Hospital, London, United Kingdom.
Ann Neurol. 1995 Jan;37(1):112-5. doi: 10.1002/ana.410370121.
A relapsing and remitting axonal polyneuropathy developed in a woman at age 47. Serial electrophysiological studies showed that the amplitudes of compound muscle action potentials and sensory action potentials were reduced but conduction velocities were only mildly slowed. F wave latencies were normal and there was no evidence of conduction block. Two sural nerve biopsy specimens showed changes supportive of axonal neuropathy. Repeated responses to prednisolone alone and later prednisolone and azathioprine suggested that inflammatory, possibly autoimmune, processes were important in this case of chronic relapsing axonal neuropathy.
一名47岁女性患复发性脱发性轴索性多发性神经病。系列电生理研究显示,复合肌肉动作电位和感觉动作电位的波幅降低,但传导速度仅轻度减慢。F波潜伏期正常,无传导阻滞证据。两份腓肠神经活检标本显示的变化支持轴索性神经病。单独使用泼尼松龙以及后来使用泼尼松龙和硫唑嘌呤的反复治疗反应提示,炎症(可能是自身免疫性)过程在该慢性复发性轴索性神经病病例中起重要作用。