Marti Sarah, Hegemann Stefan, von Büdingen Hans-Christian, Baumgartner Ralf W, Straumann Dominik
Dept. of Neurology, Zurich University Hospital, Frauenklinikstrasse 26, 8091 Zurich, Switzerland.
J Neurol. 2008 May;255(5):663-7. doi: 10.1007/s00415-008-0773-2. Epub 2008 Feb 18.
Whether the rotational vertebral artery syndrome (RVAS), consisting of attacks of vertigo, nystagmus and tinnitus elicited by head-rotation induced compression of the dominant vertebral artery (VA), reflects ischemic dysfunction of uni- or bilateral peripheral or central vestibular structures, is still debated. We report on a patient with bilateral high-grade carotid stenoses, in whom rightward headrotation led to RVAS symptoms including a prominent nystagmus. Three-dimensional kinematic analysis of the nystagmus pattern, recorded with search coils, revealed major downbeat nystagmus with minor horizontal and torsional components. Magnetic resonance angiography demonstrated a hypoplastic right VA terminating in the posterior inferior cerebellar artery, a dominant left VA, and a hypoplastic P1-segment of the left posterior cerebral artery (PCA) that was supplied by the left posterior communicating artery (PCoA). The right PCA and both anterior inferior cerebellar arteries were supplied by the basilar artery. The right PCoA originated from the right internal carotid artery. Color duplex sonography showed severe reduction of diastolic blood flow velocities in the left VA during RVAS attacks. The nystagmus pattern can be best explained by vectorial addition of 3D sensitivity vectors of stimulated right and left anterior and horizontal semicircular canals with slightly stronger stimulation on the left side. We hypothesize that in RVAS, compression of dominant VA leads to acute vertebrobasilar insufficiency with bilateral, but asymmetric ischemia of the superior labyrinth. With regard to RVAS etiology, our case illustrates a type of pure vascular RVAS. Severity of attacks markedly decreased after successful bilateral carotid endarterectomy.
由头部旋转引起的优势椎动脉(VA)受压引发眩晕、眼球震颤和耳鸣发作所构成的旋转型椎动脉综合征(RVAS),是否反映单侧或双侧外周或中枢前庭结构的缺血性功能障碍,目前仍存在争议。我们报告一名患有双侧重度颈动脉狭窄的患者,其向右旋转头部会导致RVAS症状,包括明显的眼球震颤。用搜索线圈记录的眼球震颤模式的三维运动学分析显示,主要为下跳性眼球震颤,伴有轻微的水平和扭转成分。磁共振血管造影显示,右侧椎动脉发育不全,止于小脑后下动脉,左侧椎动脉占优势,左侧大脑后动脉(PCA)的P1段发育不全,由左侧后交通动脉(PCoA)供血。右侧PCA和双侧小脑前下动脉均由基底动脉供血。右侧PCoA起源于右侧颈内动脉。彩色双功能超声显示,在RVAS发作期间,左侧椎动脉的舒张期血流速度严重降低。眼球震颤模式可以通过对刺激的右侧和左侧前半规管及水平半规管的三维敏感向量进行矢量相加来最好地解释,左侧刺激略强。我们推测,在RVAS中,优势椎动脉受压会导致急性椎基底动脉供血不足,伴有双侧但不对称的上半规管缺血。关于RVAS的病因,我们的病例说明了一种单纯血管性RVAS类型。双侧颈动脉内膜剥脱术成功后,发作的严重程度明显降低。