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特发性颅内动脉狭窄血管成形术。

Angioplasty of an idiopathic intracranial arterial stenosis.

作者信息

Layton K F, Kallmes D F, Cloft H J

机构信息

Baylor University Medical Center, Department of Radiology, Dallas, TX, USA -

出版信息

Interv Neuroradiol. 2006 Dec 15;12(4):307-11. doi: 10.1177/159101990601200403. Epub 2007 Jan 19.

Abstract

Treatment of symptomatic intracranial atherosclerotic stenosis usually involves maximizing medical therapy. In patients with medically refractory symptoms despite maximum pharmacologic therapy, intracranial angioplasty and/or stenting has become an accepted treatment option. The use of percutaneous transluminal angioplasty (PTA) for idiopathic intracranial stenoses has not been reported to date.We describe a case of idiopathic intracranial stenosis which was refractory to medical therapy and was successfully treated with percutaneous transluminal angioplasty. The presenting symptoms included multiple episodes of aphasia and right-sided weakness as well as a left basal ganglia infarct. The patient underwent treatment with two intracranial angioplasty procedures. There was a recurrence of the stenosis and symptoms following the first procedure. However, after a second treatment with a slightly larger balloon, flow in the MCA normalized. Furthermore, the symptoms attributed to her MCA stenosis had essentially resolved. This case suggests that patients with medically refractory idiopathic intracranial stenosis can be successfully treated with percutaneous transluminal angioplasty.

摘要

有症状的颅内动脉粥样硬化性狭窄的治疗通常包括优化药物治疗。对于尽管接受了最大程度的药物治疗但仍有药物难治性症状的患者,颅内血管成形术和/或支架置入术已成为一种可接受的治疗选择。迄今为止,尚未有关于经皮腔内血管成形术(PTA)用于特发性颅内狭窄的报道。我们描述了一例药物治疗无效的特发性颅内狭窄病例,该病例经皮腔内血管成形术治疗成功。患者的症状包括多次失语发作、右侧肢体无力以及左侧基底节梗死。该患者接受了两次颅内血管成形术治疗。第一次手术后出现了狭窄复发和症状。然而,在使用稍大的球囊进行第二次治疗后,大脑中动脉血流恢复正常。此外,归因于大脑中动脉狭窄的症状基本消失。该病例表明,药物难治性特发性颅内狭窄患者可通过经皮腔内血管成形术成功治疗。

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Angioplasty of an idiopathic intracranial arterial stenosis.特发性颅内动脉狭窄血管成形术。
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本文引用的文献

9
Atherosclerotic disease of the middle cerebral artery.大脑中动脉粥样硬化疾病
Stroke. 1986 Nov-Dec;17(6):1112-20. doi: 10.1161/01.str.17.6.1112.

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