[Experiences in the diagnosis and treatment of polyneuropathies in patients with malignant monoclonal gammopathy].

I Baumann, T Krause, H Schwenke, J Lehmann
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引用次数: 0

Abstract

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.

【恶性单克隆伽玛病多发神经病变的诊治体会】。
4例单克隆伽玛病患者,临床表现为感觉运动性多神经病变,病程持续数年。肌电图显示轴向衰竭和继发性脱髓鞘。在其中两例患者中发现了igg型多发性骨髓瘤,而在另外两例患者中可以证明异常IgM-mIg的增加。所有患者均发现白酒蛋白升高,且白酒中已发现适当的mIg。通过免疫荧光法在周围神经上可见相应的免疫球蛋白。神经活检的电子显微镜研究支持mig相关的多发性神经病的诊断。本文对mig相关的多神经病变的诊断和治疗进行了参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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