O'Brien B, Jackson R, Tang-Wai R, Lewis A J, Atack E A
Can J Neurol Sci. 1980 Feb;7(1):73-6.
A case of hereditary sensory neuropathy is described resembling Dyck's Type I hereditary sensory neuropathy. Sensory testing revealed marked pain impairment in feet and hands shading at mid calf to normal at mid thigh and shading above the wrist to normal at the elbow. Other sensory modalities including temperature were intact except painful heat and painful cold and they produced very little if any discomfort. Stimuli at 0 degrees C or 45 degrees to 70 degrees C elicited a temperature response but not pain. Sural nerve biopsy findings (including electromicroscopy) were consistent with a diagnosis of Type I hereditary sensory neuropathy, but also showed evidence of abortive axonal regeneration and profound Schwann cell vacuolation.
描述了一例类似于戴克 I 型遗传性感觉神经病的遗传性感觉神经病病例。感觉测试显示,足部和手部存在明显的疼痛障碍,小腿中部以下逐渐减轻,大腿中部恢复正常,手腕以上逐渐减轻,肘部恢复正常。除了痛觉热感和痛觉冷感外,包括温度觉在内的其他感觉模式均正常,且这些感觉几乎不会引起不适。0摄氏度或45至70摄氏度的刺激会引发温度反应,但不会引起疼痛。腓肠神经活检结果(包括电镜检查)与I型遗传性感觉神经病的诊断一致,但也显示出轴突再生失败和雪旺细胞明显空泡化的证据。