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卒中中液体衰减反转恢复序列血管高信号的解读

Interpretation of fluid-attenuated inversion recovery vascular hyperintensity in stroke.

作者信息

Lee Kyung-Yul, Kim Jin Woo, Park Mina, Suh Sang Hyun, Ahn Sung Jun

机构信息

Department of Neurology, Gangnam Severance Hospital, Yonsei University, College of Medicine, Seoul, Korea.

Department of Radiology, Gangnam Severance Hospital, Yonsei University, College of Medicine, Seoul, Korea.

出版信息

J Neuroradiol. 2022 May;49(3):258-266. doi: 10.1016/j.neurad.2021.01.009. Epub 2021 Jan 28.

DOI:10.1016/j.neurad.2021.01.009
PMID:33515596
Abstract

Fluid-attenuation inversion recovery (FLAIR) vascular hyperintensity (FVH) is a common presentation on brain magnetic resonance images of patients with acute ischemic stroke. This sign is known as a sluggish collateral flow. Although FVH represents the large ischemic penumbra and collateral circulation, the clinical significance of FVH has not been established. Varying protocols for FLAIR, treatment differences, and heterogeneity of endpoints across studies have complicated the interpretation of FVH in patients with acute stroke. In this review article, we describe the mechanism of FVH, as well as its association with functional outcome, perfusion-weighted images, and large artery stenosis. In addition, we review the technological variables that affect FVH and discuss the future perspectives.

摘要

液体衰减反转恢复(FLAIR)血管高信号(FVH)是急性缺血性脑卒中患者脑磁共振成像中的常见表现。该征象被称为侧支循环血流缓慢。尽管FVH代表大面积缺血半暗带和侧支循环,但FVH的临床意义尚未明确。不同的FLAIR方案、治疗差异以及各研究终点的异质性使得急性脑卒中患者FVH的解读变得复杂。在这篇综述文章中,我们描述了FVH的机制,以及它与功能结局、灌注加权成像和大动脉狭窄的关系。此外,我们回顾了影响FVH的技术变量并探讨了未来前景。

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引用本文的文献

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Cerebral hemodynamics evaluation of FLAIR vascular hyperintensity in TIA patients with large artery severe stenosis or occlusion.伴有大动脉严重狭窄或闭塞的短暂性脑缺血发作(TIA)患者中液体衰减反转恢复序列(FLAIR)血管高信号的脑血流动力学评估
Front Neurol. 2025 May 14;16:1589198. doi: 10.3389/fneur.2025.1589198. eCollection 2025.
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Comparison between MRI FLAIR vascular hyperintensity-DWI mismatch and perfusion based triage for thrombectomy in the late time window.
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Front Neurol. 2024 Jul 25;15:1400524. doi: 10.3389/fneur.2024.1400524. eCollection 2024.
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