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家族性埃布斯坦畸形中的持续性心房停搏

Persistent atrial standstill in familial Ebstein's anomaly.

作者信息

Piérard L A, Henrard L, Demoulin J C

出版信息

Br Heart J. 1985 Jun;53(6):594-7. doi: 10.1136/hrt.53.6.594.

Abstract

Persistent atrial standstill occurred in a father and his youngest son with familial Ebstein's anomaly. In both cases routine electrocardiograms showed no atrial electrical activity and cross sectional echocardiograms showed inferior displacement of the septal tricuspid leaflet and tethering of the tricuspid leaflets to the right ventricle. The father had a cerebral embolism and died of a myocardial infarction. Necropsy showed attachment of the septal tricuspid leaflet below the membranous septum. On serial histological examination fibrofatty infiltration of the right atrial wall, the atrioventricular node, and the inferior part of the His bundle up to the bifurcation was present. The son had haemodynamic and electrophysiological findings consistent with mild Ebstein's anomaly and persistent atrial standstill, for which permanent cardiac pacing was necessary. The persistent atrial standstill with slow escape rhythm was most probably a consequence of the abnormalities in both the atrial wall and the His bundle which, together with the abnormal attachment of the tricuspid valve, may be features of the same congenital cardiac anomaly.

摘要

一名患有家族性埃布斯坦畸形的父亲及其最小的儿子出现了持续性心房静止。在这两个病例中,常规心电图显示无心房电活动,心脏超声心动图显示三尖瓣隔叶向下移位以及三尖瓣叶与右心室相连。父亲发生了脑栓塞并死于心肌梗死。尸检显示三尖瓣隔叶附着于膜性间隔下方。连续组织学检查发现右心房壁、房室结以及希氏束下部直至分叉处有纤维脂肪浸润。儿子有与轻度埃布斯坦畸形和持续性心房静止相符的血流动力学和电生理表现,为此需要进行永久性心脏起搏。持续性心房静止伴缓慢逸搏心律很可能是心房壁和希氏束异常的结果,这些异常与三尖瓣的异常附着一起,可能是同一先天性心脏异常的特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2786/481820/dd1fbadaae41/brheartj00114-0011-a.jpg

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