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由胼周动脉狭窄引起的肢体抖动短暂性脑缺血发作伪装为腰椎神经根病,成功地接受了颅内血管成形术和支架置入治疗。

Limb-shaking transient ischemic attack masquerading as lumbar radiculopathy from pericallosal artery stenosis treated successfully with intracranial angioplasty and stenting.

机构信息

Department of Neurology, Medical College of Wisconsin and Froedtert Hospital, Milwaukee, WI 53226, USA.

出版信息

J Stroke Cerebrovasc Dis. 2010 Mar;19(2):169-73. doi: 10.1016/j.jstrokecerebrovasdis.2009.07.008.

Abstract

The pericallosal artery is rarely associated with intracranial atherosclerotic disease and, until recently, was usually not amenable to endovascular therapy with balloon angioplasty and stenting. We present an elderly patient with postural left leg-shaking episodes secondary to pericallosal artery stenosis, which was treated initially with primary intracranial balloon angioplasty, and subsequently, angioplasty and stenting as a result of recurrent stenosis. Both procedures were preformed without complications, and the patient remained free of symptoms on 6-month follow-up. This case demonstrates unique clinical and neuroendovascular aspects; the isolated postural leg-shaking transient ischemic attacks, initially mistaken for radiculopathy and local joint etiology, were found later to be cerebrovascular ischemic in origin. Moreover, the correlation between the findings of computed tomography perfusion and angiography localized the lesion into the medial frontal lobe and pericallosal artery territory. In addition, the technical aspect provides insight into the current state of neuroendovascular techniques, addressing the difficulty of access into very small and distal intracranial arteries affected by stenosis.

摘要

胼周动脉很少与颅内动脉粥样硬化性疾病相关,直到最近,通常不能通过球囊血管成形术和支架置入进行血管内治疗。我们介绍了一位老年患者,其因胼周动脉狭窄出现体位性左腿抖动发作,最初采用颅内原发性球囊血管成形术治疗,随后因狭窄复发而行血管成形术和支架置入术。这两种操作均无并发症,患者在 6 个月的随访中无任何症状。该病例展示了独特的临床和神经血管学方面;孤立的体位性腿部抖动短暂性脑缺血发作最初被误诊为神经根病和局部关节病因,后来发现其起源于脑血管缺血。此外,计算机断层灌注和血管造影的发现将病变定位于额内侧叶和胼周动脉区域。此外,该技术方面提供了对当前神经血管技术状态的深入了解,解决了进入受狭窄影响的非常小和远端颅内动脉的困难。

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