Apical hypertrophic cardiomyopathy associated with multiple coronary artery-left ventricular fistulae: a report of a case and review of the literature.
نویسندگان
چکیده
We present a rare case of multiple coronary artery-left ventricular (LV) fistulae, associated with apical hypertrophic cardiomyopathy in an 83-year-old woman with electrocardiographic abnormalities and a history of arterial hypertension and paroxysmal atrial fibrillation. In order to evaluate the clinical significance and obtain further insights into this unusual disease, the patient has undergone coronary angiography, left ventriculography, and magnetic resonance imaging which better substantiated the structural abnormalities of the LV and the coronary network.
منابع مشابه
Apical Hypertrophic Cardiomyopathy and Multiple Coronary Artery-left Ventricular Fistulas: a Case Report
We describe a rare case of multiple coronary artery-left ventricular fistulas associated with apical hypertrophic cardiomyopathy in a 62 year asymptomatic old male admitted to our department for a perioperative evaluation of non cardiac surgery, already diagnosed for multiple coronary artery-left fistulae. He underwent transthoracic echocardiography and then to accelerated dipiridamole stress-e...
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We report the case of a 74 year-old woman admitted for coronary angiogram because of widespread electrocardiographic repolarization abnormalities. Her past medical history was mainly paroxystic atrial fibrillation. Her cardiovascular risk factors were age and smoking. Echocardiography revealed apical left ventricular hypertrophy. Physical examination was normal. Surprisingly, the coronary angio...
متن کاملCombined apical hypertrophic cardiomyopathy and coronary artery-left ventricular fistula.
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A 40 year old male, a known case of hypertrophic cardiomyopathy, was admitted for catheterization. At catheterization and angiography, septum was hypertrophied to about 5cm and diffuse coronary artery aneurysm was revealed. We found no previous report of coronary artery aneurysm in hypertrophic cardiomyopathy.
متن کاملApical Hypertrophic Cardiomyopathy in a Case with Chest Pain and Family History of Sudden Cardiac Death: A Case Report
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disease, which is caused by a multitude of mutations in genes encoding proteins of the cardiac sarcomere (1). Apical hypertrophic cardiomyopathy (AHCM) is an uncommon type of HCM. The sudden cardiac death is less likely to occur in the patients inflicted with AHCM (2). Herein, we presented the case of a 29-year-old man ...
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ورودعنوان ژورنال:
- European journal of echocardiography : the journal of the Working Group on Echocardiography of the European Society of Cardiology
دوره 11 4 شماره
صفحات -
تاریخ انتشار 2010