Cavusoglu Yuksel, Tunerir Bulent, Birdane Alparslan, Timuralp Bilgin, Ata Necmi, Gorenek Bulent, Unalir Ahmet, Aslan Recep
Department of Cardiology, Faculty of Medicine, Osmangazi University, Eskiserhir, Turkey.
Can J Cardiol. 2005 Jun;21(8):705-7.
The present report discusses a case of noncompaction of the ventricular myocardium in a 51-year-old woman with dilated cardiomyopathy of unknown etiology. Multiple transthoracic echocardiography examinations had failed to show myocardial noncompaction, but subsequently performed transesophageal echocardiography clearly demonstrated the characteristic findings of this unusual disease. Also, an atrial septal aneurysm was identified by transesophageal echocardiography. Patients with cardiomyopathy of unknown origin should be investigated to define the presence or absence of myocardial noncompaction, even if transthoracic echocardiography fails to show anatomical features of this disease. The present case is the first reported case of ventricular noncompaction associated with an atrial septal aneurysm as a congenital anomaly.
本报告讨论了一例51岁病因不明的扩张型心肌病女性患者的心室心肌致密化不全病例。多次经胸超声心动图检查均未显示心肌致密化不全,但随后进行的经食管超声心动图清晰地显示了这种罕见疾病的特征性表现。此外,经食管超声心动图还发现了房间隔瘤。即使经胸超声心动图未能显示该疾病的解剖特征,对于病因不明的心肌病患者也应进行检查以确定是否存在心肌致密化不全。本病例是首例报道的与房间隔瘤作为先天性异常相关的心室致密化不全病例。