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浆细胞异常增生症和多发性神经病患者腓肠神经活检中的淋巴细胞。

Lymphocytes in sural nerve biopsies from patients with plasma cell dyscrasia and polyneuropathy.

作者信息

Solders G, Nennesmo I, Ernerudh J, Cruz M, Vrethem M

机构信息

Department of Neurology, Huddinge Hospital, Sweden.

出版信息

J Peripher Nerv Syst. 1999;4(2):91-8.

Abstract

Sural nerve biopsies were examined in 36 patients with plasmacell dyscrasia and polyneuropathy. The M-component isotype was IgM in 19, IgG in 16 (one patient had both IgM and IgG) and IgA in 2 patients. Five of the IgM patients had Waldenström's disease, one of the IgG cases a myeloma and two lymphoma. The remaining 28 patients had monoclonal gammopathy of uncertain significance (MGUS). Nerve conduction studies showed signs of mixed axonal/demyelinating polyneuropathy in most cases. The biopsies were evaluated with regard to nerve fibre loss, segmental demyelination and inflammatory cell infiltration. Inflammatory cells infiltrating the nerves were found in 7 of 19 IgM cases and in 6 of 16 IgG cases. Immunohistochemical staining with monoclonal antibodies to B-lymphocytes and to subsets of T-lymphocytes was performed in 33 cases. An equal distribution of CD4 and CD8 positive T cells, but no B cells, were found among the inflammatory cells. The findings indicate a possible role for cell mediated immunological mechanisms in some patients with plasma cell dyscrasia associated with polyneuropathy.

摘要

对36例浆细胞发育异常和多发性神经病患者进行了腓肠神经活检。M成分的同种型在19例中为IgM,16例中为IgG(1例患者同时有IgM和IgG),2例中为IgA。19例IgM患者中有5例患有华氏巨球蛋白血症,1例IgG患者患有骨髓瘤,2例患有淋巴瘤。其余28例患者患有意义未明的单克隆丙种球蛋白病(MGUS)。神经传导研究显示,大多数病例有混合性轴索性/脱髓鞘性多发性神经病的迹象。对活检标本进行了神经纤维丧失、节段性脱髓鞘和炎性细胞浸润方面的评估。在19例IgM病例中有7例、16例IgG病例中有6例发现有炎性细胞浸润神经。对33例进行了用抗B淋巴细胞和T淋巴细胞亚群的单克隆抗体的免疫组织化学染色。在炎性细胞中发现CD4和CD8阳性T细胞分布相等,但无B细胞。这些发现表明,在一些伴有多发性神经病的浆细胞发育异常患者中,细胞介导的免疫机制可能起作用。

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