Fazlinezhad Afsoon, Vakilian Farveh, Mirzaei Asadollah, Rastegar Azadeh Fallah
Mashhad University of Medical Sciences, Ghaem Hospital Mashhad, Iran.
J Tehran Heart Cent. 2011 Spring;6(2):85-8. Epub 2011 May 31.
Cor triatriatum sinistrum is a rare congenital cardiac malformation, accounting for about 0.1-0.4% of all congenital heart diseases and characterized by the presence of a fibromuscular membrane that subdivides the left atrium into two chambers in the classical form. While classic cor triatriatum in most patients can be observed during the neonatal period or early infancy, it is very rare in adults.We herein present an incidental finding of cor triatriatum sinistrum in a middle-aged man with coronary artery disease scheduled for coronary artery bypass graft surgery. The patient was admitted for exertional dyspnea and chest pain of a three-month duration. He had a past medical history of mild hyperlipidemia and mild hypertension. Transthoracic two-D echocardiography (TTE) demonstrated a visible presence of a membranous band in the mid portion of the left atrium with obvious obstruction by color and Doppler flow measurements, confirmed by three-D echocardiography. Selective coronary angiography also revealed a severe ostioproximal stenosis of the left anterior descending artery of up to 99%.On-pump coronary artery bypass grafting was performed without complications, during which the anastomosis of the left internal mammary artery to the left anterior descending artery and the removal of the membrane were done.
左房三房心是一种罕见的先天性心脏畸形,约占所有先天性心脏病的0.1 - 0.4%,其典型表现为存在一个纤维肌性隔膜,将左心房分为两个腔室。虽然大多数患者的典型三房心在新生儿期或婴儿早期即可观察到,但在成人中非常罕见。我们在此报告一例在计划进行冠状动脉搭桥手术的中年冠心病男性患者中偶然发现的左房三房心病例。该患者因持续三个月的劳力性呼吸困难和胸痛入院。他有轻度高脂血症和轻度高血压病史。经胸二维超声心动图(TTE)显示左心房中部可见一条膜状带,通过彩色和多普勒血流测量显示有明显梗阻,三维超声心动图证实了这一点。选择性冠状动脉造影还显示左前降支近端严重狭窄达99%。在体外循环下进行冠状动脉搭桥手术,无并发症发生,术中完成了左乳内动脉与左前降支的吻合以及隔膜切除。