Sudden death in a child with an unusual accessory connection

被引:7
作者
Heaven, DJ
Till, JA
Ho, SY
机构
[1] Royal Brompton & Harefield NHS Trust, Dept Paediat Cardiol, London SW3 6NP, England
[2] Royal Brompton & Harefield NHS Trust, Dept Cardiol, London SW3 6NP, England
[3] Univ London Imperial Coll Sci Technol & Med, Sch Med, Natl Heart & Lung Inst, London, England
来源
EUROPACE | 2000年 / 2卷 / 03期
关键词
Wolff-Parkinson-White syndrome; sudden death; childhood; accessory connection;
D O I
10.1053/eupc.2000.0101
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An 8-year-old boy with Wolff-Parkinson-White syndrome died suddenly whilst exercising. He had been well with no immediate preceding symptoms of an arrhythmia, and was receiving no drugs. As an infant he had suffered recurrent episodes of atrioventricular reciprocating tachycardia (AVRT) and had documented pre-excited atrial fibrillation. At electrophysiological (EP) study, the refractory periods of his two accessory pathways were less than 220 ms, Drugs were discontinued at 4 years of age when he remained asymptomatic. Autopsy confirmed a very unusual accessory pathway. It was a muscular connection between the base of the right atrial appendage and the right ventricle, distant from the annulus of the tricuspid valve. (Europace 2000; 2: 224-227) (C) 2000 The European Society of Cardiology.
引用
收藏
页码:224 / 227
页数:4
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