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周围性多发性神经病和意义未明的单克隆丙种球蛋白病

Peripheral polyneuropathy and monoclonal gammopathy of undetermined significance.

作者信息

Krol-v Straaten M J, Ackerstaff R G, De Maat C E

出版信息

J Neurol Neurosurg Psychiatry. 1985 Jul;48(7):706-8. doi: 10.1136/jnnp.48.7.706.

Abstract

The prevalence of peripheral polyneuropathy in patients with monoclonal gammopathy is known to be higher than in the general population. A prevalence as high as that in the series of Osby et al, who found clinical and/or electrophysiological evidence compatible with peripheral polyneuropathy in 15 of 21 patients has not been reported before. These results could not be confirmed in a study in which 19 patients with benign monoclonal gammopathy were investigated. In contrast there were only two patients with questionable evidence of peripheral neuropathy: one had lower limb symptoms and signs only, the other had evidence of a subclinical polyneuropathy with some abnormalities of nerve conduction.

摘要

已知单克隆丙种球蛋白病患者周围性多发性神经病的患病率高于普通人群。此前尚未有像奥斯比等人系列研究中那样高的患病率报告,他们在21例患者中有15例发现了与周围性多发性神经病相符的临床和/或电生理证据。在一项对19例良性单克隆丙种球蛋白病患者的研究中,这些结果未能得到证实。相比之下,仅有两名患者有周围神经病变的可疑证据:一名仅出现下肢症状和体征,另一名有亚临床多发性神经病的证据,伴有一些神经传导异常。

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