TCTAP A-095 An Integrated Scheme for Differentiating Hypertrophic Cardiomyopathy from Hypertensive Heart Disease
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چکیده
منابع مشابه
Echocardiographic differentiation of hypertensive heart disease and hypertrophic cardiomyopathy.
The clinical differentiation of hypertensive heart disease from hypertrophic cardiomyopathy usually presents no problem but it is less clear whether an echocardiographic distinction can always be made and, if so, what those echocardiographic criteria of difference are. It can be inferred from recent publications that when echocardiographic criteria for hypertrophic cardiomyopathy are met in hyp...
متن کاملHypertensive heart disease. A complex syndrome or a hypertensive 'cardiomyopathy'?
Hypertension is a major risk factor for cardiovascular morbidity and mortality. The presence of hypertension more than doubles the risk for coronary heart disease, including acute myocardial infarction and sudden death, and more than triples the risk of congestive heart failure as well as strokes. Patients with high blood pressure frequently have abnormalities of cardiac structure or function, ...
متن کاملCongenital heart disease associated with hypertrophic cardiomyopathy.
Experience has shown that clinical hypertrophic cardiomyopathy (HOCM, ASH) occurs in some patients with congenital heart disease, particularly simple lesions with a good natural prognosis. Its presence should be suspected when the clinical course is atypical for the basic congenital lesion or when there is unexpected cardiomegaly, an associated left sided lesion or left ventricular hypertrophy ...
متن کاملHypertrophic cardiomyopathy in a young hypertensive.
In 1957, Brock 1 described 3 patients with hypertrophic cardiomyopathy of which one of these patients had previously been hypertensive. Brock postulated that obstruction of the left ventricle outflow tract was caused by concentric hypertrophy of the subvalvular region of the left ventricle, which in turn resulted in sustained systemic hypertension. Later in 1970, Hambly 2 reported 8 cases of hy...
متن کاملA Case of Pseudo-Hypertrophic Cardiomyopathy: A Congenital Heart Disease
A 65-year-old woman with a history of diabetes and a prior diagnosis of hypertrophic cardiomyopathy was admitted to the Department of Cardiology for palpitations. Cardiac examination revealed a 3/6 holosystolic murmur over the left parasternal area. Echocardiography showed that the aorta extended from the morphological systemic ventricle (RV), which was identified by the three-leaflet tricuspid...
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ژورنال
عنوان ژورنال: Journal of the American College of Cardiology
سال: 2017
ISSN: 0735-1097
DOI: 10.1016/j.jacc.2017.03.135