Atrial Fibrillation-Induced Cardiac Shock: First Manifestation of a Congenitally Corrected Transposition of the Great Arteries in a 45-Year-Old Man
نویسندگان
چکیده
Background. The congenitally corrected transposition of the great arteries (L-TGA) is a very rare congenital heart defect, which often remains undetected for several decades of life. Case Presentation. We report on a 45-year-old man without prior history of heart disease, presenting with cardiac shock related to a first episode of tachycardic atrial fibrillation. The diagnostic work-up identified a L-TGA as the underlying cause for acute heart failure. Discussion. L-TGA is a very rare congenital heart defect, which is characterized by an atrioventricular as well as a ventriculoarterial discordance. By this means, the physiological sequence of pulmonary and systemic circulation is still maintained. On the basis of an ongoing strain of the right ventricle, which has to carry the burden of the systemic blood pressure, after more than four decades without symptoms, acute heart failure was triggered by a tachycardic atrial fibrillation.
منابع مشابه
Congenitally corrected transposition of the great arteries associated with partial anomalous pulmonary venous connection in a quinquagenarian with dextrocardia.
A 51-year old woman was treated for atrial fibrillation. A chest X-ray showed dextrocardia. Transthoracic echocardiography revealed a congenitally corrected transposition of the great arteries. Multidetector64 computerized tomography scan imaging confirmed the diagnosis (Fig. 1) and, additionally, showed a persistent left superior vena cava and a partial anomalous pulmonary venous connection (F...
متن کامل[Cardiac resynchronization in a patient with congenitally corrected transposition of the great arteries].
Congenitally corrected transposition of the great arteries is a rare heart defect that can be associated with systemic ventricular dysfunction and conduction disturbances. The use of cardiac resynchronization therapy in patients with congenital heart disease is not fully established. The authors report a case of cardiac resynchronization therapy in a 31-year-old woman with a history of congenit...
متن کاملPatients after atrial switch operation for transposition of the great arteries can not increase stroke volume under dobutamine stress as opposed to patients with congenitally corrected transposition.
BACKGROUND Patients after atrial switch operation for transposition of the great arteries have limited exercise performance. Rigid atrial baffles may cause a relative preload reduction. Previous studies have had suboptimal control groups, which ideally should consist of patients with congenitally corrected transposition of the great arteries (ccTGA) without previous heart surgery, having a syst...
متن کاملA Case of Congenitally Corrected Transposition of the Great Arteries Discovered on Coronary Computed Tomography
Congenitally corrected transposition of the great arteries is a rare condition accounting for less than 1% of all congenital cardiac diseases. The fundamental nature of this condition involves a blend of atrioventricular as well as ventriculoarterial discordance. Congenitally corrected transposition of the great arteries is classically associated with three additional abnormalities, including v...
متن کاملCongenitally corrected transposition of great arteries in 76-year-old woman.
A 76-year-old woman with no cardiac history was admitted to our hospital for knee joint surgery. The ECG showed negative T wave in leads I, aVL, V3-V6. Transthoracic echocardiography showed diffuse mild hypokinesis and prominent trabeculations of the left side ventricle (Picture 1). Mild aortic regurgitation and mild left atrioventricular regurgitation were also observed. Contrast-enhanced thre...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
دوره 2012 شماره
صفحات -
تاریخ انتشار 2012