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利妥昔单抗成功治疗两例意义未明的IgM单克隆丙种球蛋白病(MGUS)性神经病变

[Successful treatment with rituximab in two cases of IgM-monoclonal gammopathy of undetermined significance (MGUS) neuropathy].

作者信息

Koike Michiaki, Sugimoto Keiji, Tusui Miyuki, Yahata Yuriko

机构信息

Department of Hematology, Juntendo University Shizuoka Hospital.

出版信息

Rinsho Ketsueki. 2012 Apr;53(4):450-4.

Abstract

A 66-year-old male was hospitalized with muscle weakness and gait disturbance. Examination revealed IgM 3,407 mg/dl (IgM, κ-type M protein) and he was diagnosed as having IgM-MGUS neuropathy. He suffered from paralysis of respiratory muscles and required a respirator support. Plasmapheresis and intravenous immunoglobulin were performed and he was weaned from the respirator. Rituximab given as 8 weekly infusions improved gait disturbance. A 71-year-old male was hospitalized with lumbago, numbness of lower extremities and gait disturbance. Examination revealed IgM 1,553 mg/dl (IgM, λ-type M protein) and he was diagnosed with IgM-MGUS neuropathy. Rituximab given as 8 weekly infusions improved gait disturbance. It was concluded that rituximab is a well-tolerated treatment that may be effective in some patients with IgM-MGUS neuropathy.

摘要

一名66岁男性因肌肉无力和步态障碍入院。检查发现IgM为3407mg/dl(IgM,κ型M蛋白),他被诊断为IgM型意义未明的单克隆丙种球蛋白病(IgM-MGUS)性神经病变。他出现了呼吸肌麻痹,需要呼吸机支持。进行了血浆置换和静脉注射免疫球蛋白治疗,他成功脱离了呼吸机。每8周静脉输注一次利妥昔单抗改善了步态障碍。一名71岁男性因腰痛、下肢麻木和步态障碍入院。检查发现IgM为1553mg/dl(IgM,λ型M蛋白),他被诊断为IgM-MGUS性神经病变。每8周静脉输注一次利妥昔单抗改善了步态障碍。得出的结论是,利妥昔单抗是一种耐受性良好的治疗方法,可能对一些IgM-MGUS性神经病变患者有效。

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