Sands Kara A, Shahripour Reza Bavarsad, Kumar Gyanendra, Barlinn Kristian, Lyerly Michael J, Haršány Michal, Cure Joel, Yakov Yuri L, Alexandrov Anne W, Alexandrov Andrei V
Comprehensive Stroke Center, Department of Neurology, University of Alabama at Birmingham, Birmingham, AL, USA.
Dresden University Stroke Center, University of Technology Dresden, Dresden, Germany.
J Neuroimaging. 2016 Sep;26(5):499-502. doi: 10.1111/jon.12338. Epub 2016 Apr 8.
Isolated central facial palsy (I-CFP) is attributed to a lacunar syndrome affecting the corona radiata region or pons. We examined our acute stroke registry for patients presenting with I-CFP and localized their symptoms to a vascular lesion.
SUBJECT & METHODS: Our database of consecutive patients with symptoms of acute cerebral ischemia admitted from January 2008 to December 2012 was reviewed for NIH Stroke Scale (NIHSS) scores and subcomponents. All patients with I-CFP ± dysarthria (total NIHSS ≤ 3) had contrast-enhanced MR-angiography and transcranial Doppler as standard of care. All ischemic lesions were localized by MRI within 72 hours from symptom onset.
Of 2,202 patients with acute cerebral ischemia, 879 patients (35%) had NIHSS score ≤ 3 points (mean age 63 + 15 years, 46 % women). Nine patients (.4%) presented with I-CFP ± dysarthria. Of these, only 1 had a lesion in the corona radiata and patent MCA, 1 had a pontine lesion without proximal vessel occlusion (2/9, or 22%). Remaining 7 patients (78%) had flow-limiting thromboembolic mid-to-distal M1/proximal M2 MCA disease. Of these, 6 (86%) patients had a prominent early anterior temporal artery on MRA and nonlacunar ischemic lesions on MRI.
Contrary to current teaching of lesion localization for an I-CFP, our study revealed the majority of acute patients presenting with this symptom had evidence of flow-limiting thromboembolic MCA disease rather than a lacunar lesion. Our findings underscore the essential role of comprehensive vascular imaging in patients presenting with I-CFP, which is commonly associated with acute flow-limiting thromboembolic MCA disease.
孤立性中枢性面瘫(I-CFP)归因于影响放射冠区或脑桥的腔隙综合征。我们在急性卒中登记系统中检查了表现为I-CFP的患者,并将其症状定位到血管病变。
回顾我们2008年1月至2012年12月收治的有急性脑缺血症状的连续患者数据库,以获取美国国立卫生研究院卒中量表(NIHSS)评分及子项目。所有I-CFP ± 构音障碍(NIHSS总分≤3)的患者均接受了对比增强磁共振血管造影和经颅多普勒检查作为标准治疗。所有缺血性病变均在症状发作后72小时内通过MRI定位。
在2202例急性脑缺血患者中,879例(35%)NIHSS评分≤3分(平均年龄63 ± 15岁,46%为女性)。9例(0.4%)表现为I-CFP ± 构音障碍。其中,仅1例在放射冠区有病变且大脑中动脉(MCA)通畅,1例有脑桥病变且近端血管无闭塞(9例中的2例,即22%)。其余7例(78%)有导致血流受限的血栓栓塞性中至远端M1/近端M2 MCA病变。其中,6例(86%)患者在MRA上有明显的早期颞前动脉,且MRI上有非腔隙性缺血性病变。
与目前关于I-CFP病变定位的教学内容相反,我们的研究显示,大多数表现为此症状的急性患者有导致血流受限的血栓栓塞性MCA疾病的证据,而非腔隙性病变。我们的研究结果强调了全面血管成像在I-CFP患者中的重要作用,I-CFP通常与急性血流受限的血栓栓塞性MCA疾病相关。