Oh S J
Arch Neurol. 1978 Aug;35(8):509-16. doi: 10.1001/archneur.1978.00500320029007.
Ten patients with subacute demyelinating neuropathy responded satisfactorily to corticosteroid treatment. The most prominent features in these cases were (1) subacute progression of diffuse polyneuropathy over weeks and months, (2) high spinal fluid protein level, (3) marked nerve conduction abnormalities, and (4) high rate of relapse. The sural nerve biopsy specimen showed "demyelinating neuropathy." This subacute demyelination neuropathy appears to be a distinct and clinically identifiable entity in which corticosteroid treatment is indicated.
10例亚急性脱髓鞘性神经病患者对皮质类固醇治疗反应良好。这些病例最突出的特征是:(1)弥漫性多发性神经病在数周和数月内呈亚急性进展;(2)脑脊液蛋白水平高;(3)明显的神经传导异常;(4)复发率高。腓肠神经活检标本显示为“脱髓鞘性神经病”。这种亚急性脱髓鞘性神经病似乎是一种独特的、临床上可识别的疾病实体,对此需要进行皮质类固醇治疗。