Ozdöl Cağdaş, Akyürek Omer, Güldal Muharrem, Karaoğuz Remzi, Oral Derviş
Int J Cardiol. 2004 Feb;93(2-3):285-7. doi: 10.1016/S0167-5273(03)00152-9.
Congenital coronary sinus anomalies are unusual and they rarely coexist with accessory atrioventricular pathways. These anomalies are generally asymptomatic, however they can cause difficulty in mapping. The association between accessory pathway and coronary sinus anomalies may suggest an embryologic link. In this case, we report a male patient with permanent form of reciprocating tachycardia coexistent with anomalous coronary sinus.
先天性冠状窦异常较为罕见，且很少与房室旁道并存。这些异常通常无症状，但可能会在标测时造成困难。房室旁道与冠状窦异常之间的关联可能提示存在胚胎学联系。在此病例中，我们报告一名患有永久性折返性心动过速且并存异常冠状窦的男性患者。
