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一名患有冷球蛋白血症和抗MAG IgM单克隆丙种球蛋白病患者的血管炎性神经病变。

Vasculitic neuropathy in a patient with cryoglobulinemia and anti-MAG IGM monoclonal gammopathy.

作者信息

Thomas F P, Lovelace R E, Ding X S, Sadiq S A, Petty G W, Sherman W H, Latov N, Hays A P

机构信息

Department of Pathology, College of Physicians and Surgeons, Columbia University, New York, New York.

出版信息

Muscle Nerve. 1992 Aug;15(8):891-8. doi: 10.1002/mus.880150805.

Abstract

A patient with sensorimotor mononeuritis multiplex had a type II cryoglobulin with an IgM kappa M-protein that appeared to contain monoclonal anti-MAG antibodies of the same isotype. A sural nerve biopsy demonstrated necrotizing arteritis and features of both axonal degeneration and demyelination. IgM kappa and C3 deposits were present on the myelin sheath of some residual nerve fibers. The findings suggest that the anti-MAG antibodies contributed to the myelin damage, while cryoprecipitates may have caused the vasculitis and axonal degeneration.

摘要

一名患有感觉运动性多灶性单神经炎的患者,其II型冷球蛋白含有IgM κ M蛋白,该蛋白似乎包含相同同种型的单克隆抗MAG抗体。腓肠神经活检显示坏死性动脉炎以及轴索性变性和脱髓鞘的特征。一些残留神经纤维的髓鞘上存在IgM κ和C3沉积。这些发现表明,抗MAG抗体导致了髓鞘损伤,而冷沉淀物可能引发了血管炎和轴索性变性。

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