Ince P G, Shaw P J, Fawcett P R, Bates D
Neurology. 1987 Jul;37(7):1231-5. doi: 10.1212/wnl.37.7.1231.
A 53-year-old man presented with a painful, demyelinating sensorimotor peripheral neuropathy with lymphomatous infiltration on sural nerve biopsy, but no evidence of systemic lymphoma. The neuropathy responded to cytotoxic therapy. Seven years later he developed generalized lymphadenopathy due to B cell lymphoplasmacytoid lymphoma, with a subpopulation of cells expressing a monoclonal pattern of IgM kappa. The lymphomatous infiltrate in the original nerve biopsy showed similar monoclonal IgM kappa reactivity. The mechanism of demyelination of the peripheral nerves may be similar to that described in patients with IgM kappa monoclonal gammopathies.
一名53岁男性表现为疼痛性脱髓鞘感觉运动性周围神经病,腓肠神经活检显示有淋巴瘤浸润,但无系统性淋巴瘤证据。该神经病对细胞毒性治疗有反应。7年后,他因B细胞淋巴浆细胞样淋巴瘤出现全身淋巴结肿大,有一群细胞表达单克隆IgM κ型。原神经活检中的淋巴瘤浸润显示出类似的单克隆IgM κ反应性。周围神经脱髓鞘的机制可能与IgM κ单克隆丙种球蛋白病患者中描述的机制相似。