Ulucam Melek, Muderrisoglu Haldun, Sezgin Atilla
Department of Cardiology, Baskent University Faculty of Medicine, Ankara, Turkey.
Int J Cardiovasc Imaging. 2005 Apr-Jun;21(2-3):225-30. doi: 10.1007/s10554-004-2460-4.
The giant congenital intrapericardial aneurysmal dilatation of the left atrial appendage without mitral valve disease is a very rare condition that is generally diagnosed in older patients. The problem is usually accompanied with supraventricular rhythm disorders and life-threatening systemic thromboembolism. Complete surgical correction is possible, and it should be performed immediately after the diagnosis. We are going to describe a patient with a history of cerebral thromboembolism and palpitation who was diagnosed with congenital intrapericardial aneurysmal dilatation of the left atrial appendage. The condition was identified by means of echocardiography and was surgically treated by resection of the appendage containing the aneurysm.
无二尖瓣疾病的巨大先天性心包内左心耳瘤样扩张是一种非常罕见的疾病,通常在老年患者中被诊断出来。该问题通常伴有室上性心律失常和危及生命的系统性血栓栓塞。完全手术矫正可行,应在诊断后立即进行。我们将描述一名有脑血栓栓塞和心悸病史的患者,该患者被诊断为先天性心包内左心耳瘤样扩张。通过超声心动图确定了病情,并通过切除含有动脉瘤的心耳进行了手术治疗。