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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >A giant fusiform basilar aneurysm treated by bilateral vertebral artery occlusion.
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A giant fusiform basilar aneurysm treated by bilateral vertebral artery occlusion.

机译:双侧椎动脉闭塞治疗巨大梭状基底动脉瘤。

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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.
机译:目标和重要性。椎基底动脉的梭状动脉瘤会逐渐扩大,导致症状性脑干受压,这是危险的,而且很难治疗。描述了一种用分节的近端椎动脉显微手术闭塞成功治疗的动脉瘤患者,并简要回顾了有关这种罕见病的文献。临床表现。一名48岁病因不明的梭形基底干动脉瘤,最初表现为后循环的短暂性脑缺血发作(TIA),并因抗凝作用而终止。四年后,由于动脉瘤的大量扩张引起脑干受压,他再次出现进行性共济失调,吞咽困难和语气障碍。介入。在动脉瘤近端进行分阶段的显微手术椎动脉闭塞。仅在患者通过血管内测试气球暂时阻塞后才切断第二条(左)椎动脉。随后,动脉瘤血栓形成,远端基底动脉由一条(左)后交通动脉保持通畅。随着动脉瘤块萎缩,患者的临床状况在数月内得到了明显改善。结论。巨大的椎基底动脉瘤很少见,但存在病变,有时证明需要积极治疗。精心选择的因脑干受压而出现进行性和严重症状的患者,可以耐受近端椎动脉阻塞,前提是基底端及其所有穿孔分支有足够的侧支血流。

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