Baumann I, Krause T, Schwenke H, Lehmann J
Klinik für Innere Medizin, Karl-Marx-Universität.
Psychiatr Neurol Med Psychol (Leipz). 1990 Feb;42(2):85-95.
4 patients are reported having monoclonal gammopathies, who clinically exhibited a sensomotoric polyneuropathy being progressive during some years. The EMG showed axional failure and secondary demyelisation. In two of the patients an IgG-type multiple myeloma has been revealed, while in the other two ohnes an increase of abnormal IgM-mIg could be demonstrated. In all patients the liquor protein was found increased and the appropriate mIg has been found in the liquor. Immunohistochemically the appropriate immunoglobulins could be demonstrated on the peripheral nerve by means of immunofluorescence method. Electron microscopical studies of nerval biopsies supported the diagnosis of mIg-associated polyneuropathy. References to diagnostics and treatment of mIg-associated polyneuropathy are done.
据报道,4例患者患有单克隆丙种球蛋白病,临床上表现为感觉运动性多神经病,病程长达数年且呈进行性发展。肌电图显示轴索性损伤和继发性脱髓鞘改变。其中2例患者被诊断为IgG型多发性骨髓瘤,另外2例患者可检测到异常IgM-mIg升高。所有患者脑脊液蛋白均升高,且在脑脊液中发现了相应的mIg。通过免疫荧光法在周围神经上免疫组化显示出相应的免疫球蛋白。神经活检的电子显微镜研究支持了mIg相关多神经病的诊断。文中还提及了mIg相关多神经病的诊断和治疗。