Innominate steal syndrome–a hybrid approach

N. Camacho, C. Amaral, G. Alves, Joana Catarino, Ricardo Correira, R. Bento, M. E. Ferreira
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Abstract

The innominate and subclavian arteries are the most common locations for stenotic lesions in the upper extremities.1 Innominate steal phenomenon (ISP) is a rare clinical finding, characterized by a flow inversion of a segment or the entire carotid axis, on color duplex scan (CDS), caused by a stenosis or occlusion of the innominate artery.2 Hemodynamic findings on CDS include reversed or bidirectional flow in the right vertebral artery, midsystolic deceleration or total reversed flow in any of the branches of the right carotid axis and an elevated left common carotid artery (CCA)/right CCA ratio.2,3 Unlike subclavian steal, ISP is usually symptomatic, affecting booth posterior fossa and hemispheric cortex.4
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无名氏综合征——一种混合疗法
锁骨无名动脉和锁骨下动脉是上肢狭窄病变最常见的部位无名动脉狭窄或闭塞是一种罕见的临床表现,其特征是在彩色双工扫描(CDS)上出现一段或整个颈动脉轴的血流反转CDS的血流动力学表现包括右椎动脉的反向或双向血流,右颈动脉轴任何分支的收缩中期减速或完全反向血流,左颈总动脉(CCA)/右颈总动脉(CCA)比值升高。与锁骨下窃血不同,ISP通常是有症状的,影响后窝和半球皮质
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