Chazot G, Berger B, Carrier H, Barbaret C, Bady B, Dumas R, Creyssel R, Schott B
Rev Neurol (Paris). 1976 Mar;132(3):195-212.
Analysis of 105 peripheral and central nervous system complications in 1062 monoclonal gammapathies draws attention to two types of phenomena. The possibility of pure neurological manifestations of IgM monoclonal gammapathies with macroglobulinorachia leads to discussion of their nosological position in relation to Waldenström's disease, Burkitt's lymphoma and Marek's disease. It is suggested that these cases should be reclassified under the heading "secreting neurolymphomatosis". Immunofluorescence and electron microscopy of 10 biopsies of the peripheral nerve showed deposits of monoclonal immunoglobulin whose function in determining peripheral neuropathies is discussed. The simultaneous presence of lymphoid infiltration, amyloid deposits and the monoclonal immunoglobulin (M component) suggests that this immunoglobulin could be the link between the cellular infiltrate secreting it and amyloid infiltration which would be the visible manifestation of it.
对1062例单克隆丙种球蛋白病中的105例周围和中枢神经系统并发症进行分析后,发现了两种现象。IgM单克隆丙种球蛋白病伴巨球蛋白血症出现单纯神经表现的可能性,引发了关于它们在与瓦尔登斯特伦病、伯基特淋巴瘤和马立克氏病相关的疾病分类学位置的讨论。有人建议,这些病例应重新归类为“分泌性神经淋巴瘤病”。对10例周围神经活检进行免疫荧光和电子显微镜检查,发现了单克隆免疫球蛋白沉积物,并讨论了其在确定周围神经病变中的作用。淋巴样浸润、淀粉样沉积物和单克隆免疫球蛋白(M成分)同时存在,表明这种免疫球蛋白可能是分泌它的细胞浸润与淀粉样浸润之间的联系,而淀粉样浸润可能是其明显表现。