沃尔夫-帕金森-怀特综合征合并右心房动脉瘤1例。

Meryem Beyazal, Senem Özgür
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引用次数: 0

摘要

沃尔夫-帕金森-怀特综合征很少与右心房动脉瘤相关。但是,一旦出现这种情况,只要动脉瘤存在,就会引起预兴奋,很难控制。1例14岁女性患者因不规则宽QRS复合心动过速在我中心急诊治疗,体表心电图出现预兴奋型。一项初步的电生理研究显示,右侧后副通路对射频和灌洗射频消融均有抵抗性。随后,透视显示这是由右心房动脉瘤引起的。虽然在第二次手术中成功地进行了射频冲洗消融,但由于动脉瘤的关联,该手术被认为是次优的。因此,我们开始了抗血栓和抗心律失常药物治疗。我们决定不做手术,并对该病例进行了2年的医学治疗,无并发症。在这里,我们详细报道这种罕见的共存和我们的治疗方法。
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A Rare Case of Wolff-Parkinson-White Syndrome Associated with Right Atrial Aneurysm.

Wolff-Parkinson-White syndrome is rarely associated with a right atrial aneurysm. However, when such a condition occurs, it will be hard to manage since pre-excitation will be induced as long as the aneurysm persists. A 14-year-old female patient received emergency treatment for irregular wide QRS complex tachycardia in our center, and a pre-excitation pattern was then observed on the surface electrocardiogram. An initial electrophysiological study revealed a high-risk right posterior accessory pathway that was resistant to both radiofrequency and irrigated radiofrequency ablations. Subsequently, fluoroscopy showed that this was due to a right atrial aneurysm. Although successful ablation with irrigated radiofrequency was performed in the second procedure, the procedure was considered suboptimal due to the association of aneurysm. Accordingly, we initiated anti-thrombotic and anti-arrhythmic drug therapy. We decided to omit surgery and followed the case under medical treatment for 2 years without complications. Here, we report this rare coexistence and our treatment approach in detail.

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来源期刊
CiteScore
1.30
自引率
12.50%
发文量
124
审稿时长
32 weeks
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