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一例经双侧椎动脉闭塞治疗的巨大梭形基底动脉瘤。

A giant fusiform basilar aneurysm treated by bilateral vertebral artery occlusion.

作者信息

Omahen David A, Findlay J Max

机构信息

Division of Neurosurgery, Department of Surgery, University of Alberta, Edmonton, Canada T6G 2B7.

出版信息

J Clin Neurosci. 2004 Apr;11(3):324-8. doi: 10.1016/j.jocn.2003.06.002.

Abstract

OBJECTIVE AND IMPORTANCE

Fusiform aneurysms of the vertebrobasilar arteries that progressively enlarge causing symptomatic brainstem compression are dangerous and their treatment is difficult. A patient with such an aneurysm treated successfully with staged, microsurgical occlusions of the proximal vertebral arteries is described, and the literature pertaining to this rare condition is briefly reviewed.

CLINICAL PRESENTATION

A 48-year-old man with a fusiform basilar trunk aneurysm of uncertain etiology presented initially with transient ischemic attacks (TIAs) of the posterior circulation that ceased with anticoagulation. Four years later he presented again with progressive ataxia, dysphagia and dysphonia due to considerable enlargement of the aneurysm causing brainstem compression.

INTERVENTION

Staged microsurgical vertebral artery occlusions proximal to the aneurysm were performed. The second (left) vertebral artery was clipped only after the patient passed its temporary occlusion with an endovascular test balloon. The aneurysm subsequently thrombosed, the distal basilar artery kept patent by a single (left) posterior communicating artery. The patient's clinical condition improved markedly over a number of months as the aneurysm mass atrophied.

CONCLUSION

Giant vertebrobasilar aneurysms are rare but treacherous lesions, sometimes justifying aggressive management. Carefully selected patients with progressive and severe symptoms due to brainstem compression may tolerate proximal vertebral artery occlusions, provided there is adequate collateral flow to the basilar termination and all of its perforating branches.

摘要

目的及重要性

椎基底动脉梭形动脉瘤逐渐增大并导致有症状的脑干受压,此类动脉瘤很危险且治疗困难。本文描述了一名通过分期显微手术闭塞椎动脉近端成功治疗的此类动脉瘤患者,并简要回顾了有关这种罕见病症的文献。

临床表现

一名48岁男性,患有病因不明的基底动脉主干梭形动脉瘤,最初表现为后循环短暂性脑缺血发作(TIA),经抗凝治疗后发作停止。四年后,由于动脉瘤显著增大导致脑干受压,他再次出现进行性共济失调、吞咽困难和发音障碍。

干预措施

在动脉瘤近端进行分期显微手术闭塞椎动脉。仅在患者通过血管内测试球囊对第二(左)椎动脉进行临时闭塞后,才对其进行夹闭。动脉瘤随后血栓形成,基底动脉远端通过单一(左)后交通动脉保持通畅。随着动脉瘤肿块萎缩,患者的临床状况在数月内明显改善。

结论

巨大椎基底动脉瘤罕见但危险,有时需要积极治疗。对于因脑干受压而出现进行性严重症状的精心挑选的患者,若基底动脉末端及其所有穿支有足够的侧支血流,则可能耐受椎动脉近端闭塞。

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