首页> 外文期刊>The Internet Journal of Neurology >Writer's cramp as a clinically isolated syndrome
【24h】

Writer's cramp as a clinically isolated syndrome

机译:作家抽筋为临床孤立综合征

获取原文
       

摘要

We present a case of writer's cramp in a patient whom cranial T2 weighted MRI showed lesions in the lentiform nucleus, putamen and the internal capsule. Following the extensive work-up for the differential diagnosis of multiple sclerosis, the patient was defined as clinically isolated syndrome. The patient's symptoms resolved after intravenous methylprednisolone treatment. To our knowledge this is the first case of writer's cramp with clinically isolated syndrome in the literature. Introduction Clinically isolated syndrome (CIS) was defined as an acute or subacute episode affecting one region of the CNS especially the optic nerves, brain stem or spinal cord that is presumed to be demyelinating, with no previous history of possible demyelinating event [1, 2]. Approximately 90% of patients with multiple sclerosis (MS) initially present with CIS [2]. In most instances symptoms and signs indicate a lesion in the optic nerve, spinal cord or brain stem in an order of decreasing frequency [1,3]. Tremor, tonic spasm, ballism, palatal and other types of myocloni, dystonia, and parkinsonism due to demyelinating lesions in critical regions are known to result in such movement disorders. Movement disorders other than tremor, associated with MS occur infrequently [4]. The association of most cases of dystonia including writer's cramp (WC) with MS was thought as coincidental. Two patients described in the literature with WC have the diagnosis of laboratory supported definite MS according to the Poser's criteria [4]. The present case with WC was discussed as CIS. Case report A 45-year-old man presented with writer's cramp that appeared one year ago. Initial neurological examination revealed bilateral slight postural and kinetic tremors in addition to writer's cramp which has been associated with dystonic posturing of elbow, thumb and index finger. The cranial MRI showed multiple hyperintense lesions on T2-weighted sequences (figure 1) in periventricular and subcortical white matter (lentiform nucleus, putamen and the internal capsule), subsequently enhancing on T1-weighted sequences (figure 1).
机译:我们介绍了一名颅骨T2加权MRI表现为大肠状核,壳状核和内囊病变的患者的绞痛病例。在对多发性硬化症进行鉴别诊断的广泛研究之后,该患者被定义为临床孤立综合征。静脉注射甲基泼尼松龙治疗后患者症状缓解。据我们所知,这是文学史上第一例患有临床孤立综合征的抽筋病例。简介临床孤立综合征(CIS)定义为一种急性或亚急性发作,影响中枢神经系统的一个区域,特别是视神经,脑干或脊髓,这些区域被认为具有脱髓鞘作用,而以前没有发生过脱髓鞘事件的历史[1、2 ]。最初有CIS的多发性硬化症(MS)患者中约有90%[2]。在大多数情况下,症状和体征表明视神经,脊髓或脑干有病变,且频率递减[1,3]。已知由于关键区域的脱髓鞘性病变引起的震颤,强直性痉挛,弹道、,肌和其他类型的肌阵挛,肌张力障碍和帕金森氏症会导致此类运动障碍。除震颤外,与MS相关的运动障碍很少发生[4]。大多数肌张力障碍病例包括作家的抽筋(WC)与MS的关联被认为是偶然的。文献中描述的两名WC患者根据Poser的标准诊断为实验室支持的确诊MS [4]。带有WC的本案被称为CIS。病例报告一年前出现的一名45岁男子出现了作家的抽筋。最初的神经系统检查发现,除了作家的抽筋外,双侧还有轻微的姿势性和运动性震颤,这与肘部,拇指和食指的肌张力异常有关。颅脑MRI在脑室周围和皮层下白质(齿状核,壳核和内囊)的T2加权序列(图1)上显示多个高强度病变,随后在T1加权序列上增强(图1)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号