| Literature DB >> 15858948 |
Gulumser Heper1, Sedat Kose, Ayhan Kilic, Basri Amasyali, Ersoy Isik.
Abstract
Congenital nonfamilial supravalvular aortic stenosis (SVAS) is relatively rare, its diffuse type being the least common. We present a 30-year-old woman with diffuse SVAS complicated with left ventricular apical aneurysm. We believe that subtle left ventricular myocardial ischemia or infarction and long-lasting severe pressure overload to the apical chamber caused LV apical aneurysm in our case. Acquired LV apical aneurysm secondary to supravalvular aortic stenosis, in the absence of atherosclerotic coronary artery disease and hypertrophic obstructive cardiomyopathy, has not been described before.Entities:
Mesh:
Year: 2005 PMID: 15858948 DOI: 10.1536/ihj.46.153
Source DB: PubMed Journal: Int Heart J ISSN: 1349-2365 Impact factor: 1.862