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多发性硬化症最初表现为偏头痛症状恶化。

Multiple sclerosis presenting initially with a worsening of migraine symptoms.

机构信息

Department of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.

出版信息

J Headache Pain. 2013 Aug 9;14(1):70. doi: 10.1186/1129-2377-14-70.

Abstract

Multiple sclerosis (MS) is a chronic autoimmune disease that targets myelinated axons in the central nervous system. Headache has been reported as a subtle symptom of the onset of MS, with a variable frequency of 1.6-28.5%; however, it remains unclear whether headache is a true symptom of MS onset. Here, we report the case of a female patient who had a history of migraine without aura and experienced worsening of migraine-headache symptoms as the initial manifestation of MS. Three similar cases were reported previously; however, unlike this case, those cases had no history of migraine without aura. In our case, we excluded factors that could trigger migraine attacks, such as changes in weather, drugs, alcohol, caffeine withdrawal, stress, fatigue, lack of sleep, hormonal therapy, diet, and hunger. The patient had one episode of MS attack with the simultaneous presence of asymptomatic gadolinium-enhancing and non-enhancing lesions, including hyperintense lesions in the bilateral periventricular white matter, body of the corpus callosum, and periaqueductal grey matter, as observed on the T2-weighted images obtained at the first brain magnetic resonance imaging. In addition, after the injection of gadolinium contrast, ring enhancement over these lesions was noted in T1-weighted images, which was suggestive of active demyelination. MS was diagnosed according to the McDonald criteria (2010 revision). We conclude that MS with periaqueductal grey matter involvement may present with worsening migraine. It is important to be cautious if any secondary causes exist, especially when the patient has a history of migraine without aura. MS should be one of the differential diagnoses in young women showing a change in headache pattern or poor clinical drug response to migraine treatment accompanied by episodes of focal neurological deficit. Failure to recognize MS may lead to inappropriate treatment and worse prognosis; early diagnosis in patients with MS is essential to improve their clinical outcomes and quality of life.

摘要

多发性硬化症 (MS) 是一种慢性自身免疫性疾病,其靶器官是中枢神经系统中的髓鞘轴突。头痛已被报道为 MS 发病的微妙症状,其发生率为 1.6-28.5%;然而,目前尚不清楚头痛是否是 MS 发病的真正症状。在这里,我们报告了一例有先兆偏头痛病史的女性患者,其 MS 发病的最初表现为偏头痛头痛症状恶化。先前曾报道过三例类似病例;然而,与本病例不同的是,这些病例均无先兆偏头痛病史。在我们的病例中,我们排除了可能引发偏头痛发作的因素,如天气变化、药物、酒精、咖啡因戒断、压力、疲劳、睡眠不足、激素治疗、饮食和饥饿。该患者有一次 MS 发作,同时存在无症状钆增强和非增强病变,包括双侧脑室周围白质、胼胝体体部和导水管周围灰质的高信号病变,这些病变在首次脑部磁共振成像的 T2 加权图像上观察到。此外,在注射钆造影剂后,这些病变在 T1 加权图像上可见环形增强,提示活跃性脱髓鞘。根据 McDonald 标准(2010 年修订版)诊断为 MS。我们得出结论,累及导水管周围灰质的 MS 可能表现为偏头痛恶化。如果存在继发性原因,尤其是患者有先兆偏头痛病史时,应谨慎对待。对于表现出头痛模式改变或偏头痛治疗效果不佳且伴有局灶性神经功能缺损发作的年轻女性,MS 应作为鉴别诊断之一。如果未能识别出 MS,可能会导致治疗不当和预后较差;早期诊断 MS 对改善患者的临床结局和生活质量至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2a6/3751257/960452adc6c6/1129-2377-14-70-1.jpg

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