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伴有近端运动轴索性神经病的球蛋白病,酷似运动神经元病。

Gammopathy with proximal motor axonopathy simulating motor neuron disease.

作者信息

Parry G J, Holtz S J, Ben-Zeev D, Drori J B

出版信息

Neurology. 1986 Feb;36(2):273-6. doi: 10.1212/wnl.36.2.273.

Abstract

We report a 38-year-old man with a pure motor syndrome and IgM gammopathy leading to flaccid quadriplegia. Improvement followed treatment with dexamethasone, cyclophosphamide, and plasmapheresis, but he died of pulmonary embolism. At autopsy, he had a proximal motor axonopathy with lymphocytic infiltration of ventral roots. Proximal motor neuropathy may masquerade as motor neuron disease. The association with gammopathy and response to treatment suggest that patients with motor neuron disease should be routinely screened for serum protein abnormalities.

摘要

我们报告了一名38岁男性,患有纯运动综合征和IgM丙种球蛋白病,导致弛缓性四肢瘫痪。经地塞米松、环磷酰胺和血浆置换治疗后病情改善,但他死于肺栓塞。尸检时,他患有近端运动轴索性神经病,腹侧神经根有淋巴细胞浸润。近端运动神经病可能会伪装成运动神经元病。与丙种球蛋白病的关联以及对治疗的反应表明,对于运动神经元病患者应常规筛查血清蛋白异常情况。

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