卡达西,偏头痛和多发性硬化症(MS)-误诊的风险,病例报告

Piotr Bogucki, P. Felczak, T. Wierzba-Bobrowicz, H. Sienkiewicz-Jarosz, U. Fiszer
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引用次数: 0

摘要

多发性硬化症(MS)的诊断标准多年来一直在变化,以使诊断更容易、更快速,特别是在过去十年。它们可以使多发性硬化症患者得到更早的治疗,从而使患者更有可能保持健康和工作能力。时间传播(DIT)和空间传播(DIS)是诊断多发性硬化症所必需的一般规则,至今已发表的所有诊断标准都保持了这一规则[1]。目前的标准于2017年发布,甚至可以在以前无法诊断出多发性硬化症的患者中诊断出多发性硬化症。这是因为没有DIT的DIS患者存在CSF寡克隆带足以诊断MS[2]。脑常染色体显性动脉病变伴皮质下梗死和脑白质病(CADASIL)是一种与NOTCH3基因突变相关的小血管疾病,可导致先兆偏头痛、复发性缺血性发作、认知障碍和行为障碍等症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cadasil, Migraine and Multiple Sclerosis (MS)-The Risk of Misdiagnosis, Case Report
Diagnostic criteria for multiple sclerosis (MS) have been changing for years to enable easier and faster ways to confirm diagnosis especially during last decade. They lead to earlier treatment of patients with MS what gives higher likelihood to keep patients fit and capable of working. Dissemination in time (DIT) and in space (DIS) are general rules which are necessary to diagnose MS what was maintained in all diagnostic criteria, which have been published up till now[1]. Current criteria were published in 2017 and enable diagnosing MS even in patients, who earlier could not have MS diagnosed. This results from the facts that CSF oligoclonal bands present in patients with DIS without DIT are enough to MS diagnose[2]. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a disease of small vessels related to gene NOTCH3 mutations leading to symptoms of migraine with aura, recurrent ischemic incidences, cognitive impairment and behavioral disturbance.
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