Julien J, Vital C, Vallat J M, Lagueny A, Ferrer X, Leboutet M J
Neurology. 1984 Oct;34(10):1387-9. doi: 10.1212/wnl.34.10.1387.
A chronic demyelinating neuropathy with "benign" IgM gammopathy was followed for 6 years in a 63-year-old man. The clinical, biologic, and EMG aspects were similar to those already reported, but a lymphoplasmocytic infiltrate in the nerve connective tissue of this patient has only rarely been observed in benign IgM gammopathy. The paraprotein was not evident in the serum until 5 years after symptoms of the neuropathy started.
一名63岁男性的慢性脱髓鞘性神经病变伴“良性”IgM型丙种球蛋白病被随访了6年。其临床、生物学及肌电图表现与已报道的相似,但该患者神经结缔组织中的淋巴细胞浆细胞浸润在良性IgM型丙种球蛋白病中仅很少被观察到。直到神经病变症状出现5年后,血清中的副蛋白才变得明显。