Smith I S, Kahn S N, Lacey B W, King R H, Eames R A, Whybrew D J, Thomas P K
Brain. 1983 Mar;106 (Pt 1):169-95. doi: 10.1093/brain/106.1.169.
Twelve cases of chronic sensorimotor neuropathy associated with benign IgM paraproteinaemia are described. The onset was in the sixth or seventh decades and 9 cases were male. Tremor and ataxia were common features. The ESR was raised in 6 cases and the CSF protein content elevated in 10. There was severe reduction of motor nerve conduction velocity. Sera from all cases contained monoclonal IgM antibodies strongly reactive with human peripheral myelin, made up by the paraprotein. Histological studies on nerve biopsies taken from 8 cases all demonstrated a demyelinating neuropathy. Eight biopsies were examined by immunofluorescence. Monoclonal IgM was present on the myelin sheaths of surviving myelinated nerve fibres. The findings suggested that the neuropathy was of autoimmune origin and caused directly by the antimyelin antibody.
本文描述了12例与良性IgM副蛋白血症相关的慢性感觉运动性神经病。发病年龄在六七十岁,9例为男性。震颤和共济失调是常见症状。6例血沉升高,10例脑脊液蛋白含量升高。运动神经传导速度严重降低。所有病例的血清均含有与人类周围髓鞘强烈反应的单克隆IgM抗体,由副蛋白组成。对8例患者进行的神经活检组织学研究均显示为脱髓鞘性神经病。8例活检标本进行了免疫荧光检查。在存活的有髓神经纤维的髓鞘上存在单克隆IgM。这些发现提示该神经病起源于自身免疫,由抗髓鞘抗体直接引起。