Sensorimotor polyneuropathy in light chain multiple myeloma.

G Pellegrini, G Scarlato, M Moggio, C Bettinelli, S M Gaini
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引用次数: 6

Abstract

The authors describe an adult onset sensorimotor polyneuropathy in a woman with light chain K-type myeloma. Neurophysiological investigation showed a severe reduction of conduction velocity of the peripheral nerve to the four limbs. A muscle and sural nerve biopsy were performed. Sural nerve displayed a severe loss of myelinated and unmyelinated fibers. No amyloid deposit was observed in vessels, perineurium and endomysium by electron microscopy examination. No onion bulb formation was present in nerve tissue, but many demyelinated fibers were surrounded by circumferentially disposed Schwann cell processes without any interposition of collagen fibrils. Some fibers exhibit signs of active remyelination; axonal alterations were rarely seen. Collagen pockets were frequently observed among proliferated collagen fibrils. The mechanism of peripheral nerve lesions in various categories of multiple myeloma is till now an unsolved problem. In this case the unusual association with a light chain myeloma suggest that these immunoglobulins play a role in the pathogenesis of the polyneuropathy as supported by experimental studies.

轻链多发性骨髓瘤的感觉运动多神经病变。
作者描述了一名患有轻链k型骨髓瘤的女性成人发病感觉运动多神经病变。神经生理学研究显示周围神经到四肢的传导速度严重降低。进行肌肉和腓肠神经活检。腓肠神经显示有髓和无髓纤维的严重损失。电镜检查血管、神经会膜、肌内膜未见淀粉样蛋白沉积。神经组织中未见洋葱鳞茎形成,但许多脱髓鞘纤维被周向排列的雪旺细胞突包围,未见胶原原纤维的介入。一些纤维表现出活跃的髓鞘再生的迹象;轴突改变少见。在增生的胶原原纤维中经常观察到胶原袋。各类多发性骨髓瘤周围神经病变的发生机制至今仍是一个未解之谜。在本病例中,与轻链骨髓瘤的不寻常关联表明,实验研究支持这些免疫球蛋白在多发性神经病变的发病机制中发挥作用。
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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