FHM2突变患者偏头痛发作时磁共振成像和单光子发射计算机断层扫描的神经血管变化

Q3 Medicine Cephalalgia Reports Pub Date : 2020-02-25 DOI:10.1177/2515816320908642
A. Nagai, Daiki Tanaka, K. Kuroshima, S. Ura, Kazuto Yoshida, Yuji Takahashi, I. Yabe
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引用次数: 1

摘要

本文旨在提供家族性偏瘫性偏头痛(FHM)病例的神经影像学资料。一个14岁的男性在他的第一次偏瘫性偏头痛发作期间,表现出正常的弥散加权磁共振成像(DWI)和液体衰减反转恢复(FLAIR)结果。然而,磁共振血管造影(MRA)显示右侧大脑中动脉弥漫性狭窄。脑血流-单光子发射计算机断层扫描显示右侧灌注不足。后续研究未发现异常。他的母亲在偏头痛发作期间的DWI, FLAIR和MRA检查结果正常。两例患者均被诊断为FHM2 (ATP1A2 p.R763H突变)。本研究强调了FHM2头痛期神经血管检查的重要性。需要进一步的病例来阐明偏头痛的病理生理。
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Neurovascular changes in magnetic resonance imagining and single-photon emission computed tomography during migraine attack in patients with FHM2 mutations
The aim of this article is to provide neuroimaging data on cases with familial hemiplegic migraine (FHM). A 14-year-old male presented normal diffusion-weighted magnetic resonance imaging (DWI) and fluid-attenuated inversion recovery (FLAIR) findings during his first hemiplegic migraine attack. However, magnetic resonance angiography (MRA) showed diffuse narrowing of the right middle cerebral artery. Cerebral blood flow–single-photon emission computed tomography showed right hypoperfusion. A follow-up study showed no abnormal findings. His mother had normal DWI, FLAIR, and MRA findings during her migraine attack. Both patients were diagnosed with FHM2 (p.R763H mutation in ATP1A2). This study highlights the importance of neurovascular examinations during the FHM2 headache phase. Further cases are required to clarify the pathophysiology of migraine.
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来源期刊
Cephalalgia Reports
Cephalalgia Reports Medicine-Neurology (clinical)
CiteScore
2.50
自引率
0.00%
发文量
17
审稿时长
9 weeks
期刊最新文献
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