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异环磷酰胺相关肌阵挛-脑病综合征。

Ifosfamide associated myoclonus-encephalopathy syndrome.

机构信息

Department of Neurology, Division of Movement Disorders, Mayo Clinic, 200 1st Street S.W., Rochester, MN 55905, USA.

出版信息

J Neurol. 2011 Sep;258(9):1729-31. doi: 10.1007/s00415-011-5990-4. Epub 2011 Mar 12.

Abstract

The aim of this study was to investigate the presence of movement disorders associated with ifosfamide toxicity. One of the most common adverse events of ifosfamide treatment is central nervous system toxicity. However, little is known about the occurrence of movement disorders associated with ifosfamide toxicity. We performed a retrospective computer search of the electronic medical records database of the Mayo Clinic, Rochester, MN from 1 January 1997-30 June 2010, using a series of search terms to identify all patients that had been treated with ifosfamide for systemic cancer. Among 400 patients that have ever used ifosfamide, we selected those patients that had any neurological complication in their medical records after the use of ifosfamide. Fifty-two had a neurological complication after ifosfamide administration. The most common neurological complication was encephalopathy that was present in 11 cases (21%). The presence of a movement disorder time locked to the administration of ifosfamide was reported in seven cases (13%). Generalized myoclonus was most common, occurring in four patients while postural tremor was documented in the other three. All patients with myoclonus had asterixis. Four of the patients also had encephalopathy. In six patients the movement disorders resolved within 48 h, spontaneously, after the discontinuation of ifosfamide, while in one case resolved in 24 h after the treatment with methylene blue. Our study demonstrates that although encephalopathy is the most common adverse neurological event associated with ifosfamide toxicity, movement disorders, including generalized myoclonus, asterixis, and postural tremors may also occur. Treatment with methylene blue may be further considered as useful to ameliorate the movement disorders.

摘要

本研究旨在探讨与异环磷酰胺毒性相关的运动障碍的发生情况。异环磷酰胺治疗的最常见不良事件之一是中枢神经系统毒性。然而,关于与异环磷酰胺毒性相关的运动障碍的发生情况知之甚少。我们对明尼苏达州罗彻斯特市梅奥诊所的电子病历数据库进行了回顾性计算机检索,检索时间为 1997 年 1 月 1 日至 2010 年 6 月 30 日,使用了一系列检索词来识别所有接受过异环磷酰胺全身癌症治疗的患者。在 400 名曾使用过异环磷酰胺的患者中,我们选择了在使用异环磷酰胺后病历中有任何神经并发症的患者。在异环磷酰胺给药后,52 名患者出现了神经系统并发症。最常见的神经系统并发症是脑病,有 11 例(21%)。有 7 例(13%)报告在异环磷酰胺给药时出现运动障碍。全身性肌阵挛最常见,有 4 例患者发生,另外 3 例患者出现姿势性震颤。所有肌阵挛患者均有扑翼样震颤。4 例患者还伴有脑病。在 6 例患者中,运动障碍在停用异环磷酰胺后 48 小时内自行缓解,1 例在使用亚甲蓝治疗后 24 小时内缓解。我们的研究表明,虽然脑病是与异环磷酰胺毒性相关的最常见不良神经事件,但运动障碍,包括全身性肌阵挛、扑翼样震颤和姿势性震颤也可能发生。亚甲蓝治疗可能进一步被认为是改善运动障碍的有用方法。

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