Department of Neurology, San Raffaele Scientific Institute, Milan, Italy.
Neurol Sci. 2010 Dec;31(6):829-31. doi: 10.1007/s10072-010-0352-z. Epub 2010 Jun 24.
Multifocal motor neuropathy (MMN) is a rare immune-mediated disease characterized by slowly progressive, asymmetric, predominantly distal weakness of one or more limbs without sensory loss. The first line of treatment is high-dose intravenous immunoglobulins (IVIg). Subcutaneous immunoglobulins (SCIg)already approved for the treatment of primary immune deficiency have recently been proposed also for the treatment of disimmune peripheral neuropathies such as MMN, and a few trials were performed to see if patients receiving immunomodulatory doses of IVIg could be treated equally well with SCIg. We describe a patient affected by MMN who was included in a protocol of treatment with SCIg for a period of 6 months. He successfully responded to treatment with a stabilization of strength. The patient is still treated with SCIg even after the end of the protocol. This is the first description of an Italian case of a patient affected by MMN successfully treated with SCIg.
多灶性运动神经病(MMN)是一种罕见的免疫介导疾病,其特征为进行性缓慢、不对称、主要累及一个或多个肢体的远端无力,无感觉丧失。一线治疗是大剂量静脉注射免疫球蛋白(IVIg)。已批准用于治疗原发性免疫缺陷的皮下免疫球蛋白(SCIg)最近也被提议用于治疗免疫性周围神经病,如 MMN,并且已经进行了一些试验来观察接受免疫调节剂量 IVIg 的患者是否可以同样接受 SCIg 治疗。我们描述了一位患有 MMN 的患者,他被纳入了一项 SCIg 治疗方案,为期 6 个月。他成功地对治疗做出了反应,力量得到了稳定。即使在方案结束后,患者仍继续接受 SCIg 治疗。这是首例成功接受 SCIg 治疗的意大利 MMN 患者的描述。