Wolff-Parkinson-White综合征合并快速阵发性心房颤动患者的潜伏性完全房室传导阻滞

Dariusz Michałkiewicz, Sebastian Przychodzeń, Małgorzata Oleszczak-Kostyra, Andrzej Osiecki, Wacław Kochman
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引用次数: 0

摘要

Wolf-Parkinson-White (WPW)综合征很少并发完全性房室传导阻滞(AVB)。在这种情况下,心室完全通过辅助通路激活,QRS复合物宽,并表现出最大的预兴奋特征。本病例报告描述了一名68岁男性的症状性WPW综合征,快速心房颤动发作和完全性房室传导阻滞。WPW综合征的完全性心脏传导阻滞应在QRS和PJ间期非常宽、撕裂时予以怀疑;0.27 s和阵发性心房颤动,无房室再入性心动过速发作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Latent complete atrioventricular block in a patient with Wolff–Parkinson–White syndrome and fast paroxysmal atrial fibrillation
The Wolf–Parkinson–White (WPW) syndrome is very rarely complicated with a complete atrioventricular block (AVB). In this case, the ventricle is activated entirely through the accessory pathway and the QRS complex is wide and exhibits maximum pre-excitation features. This case report describes a history of a 68 years old male with symptomatic WPW syndrome, episodes of rapid atrial fibrillation and complete atrioventricular block. Complete heart block in WPW syndrome should be suspected in the presence of a very wide, torn QRS, PJ interval > 0.27 s and paroxysmal atrial fibrillation without atrioventricular re-entrant tachycardia episodes.
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