2Department of Echocardiography, Wuhan Asia Heart Hospital, Wuhan, P.R. China
CONTENT
A 54-year-old male presented to our emergency department with chest tightness and chest pain for 5 h. Physical examination was unremarkable. Laboratory tests showed elevated cardiac troponin levels with hs-cTnI 4.238 ng/L (normal value <0.0198 ng/L). Echocardiography showed ascending aortic dilatation, severe aortic valve insufficiency, and left ventricular wall thickening. Coronary computed tomographic angiography (CCTA) showed a hypoplastic left coronary cusp separated by membranous structure, and aortic valve leaflet thickness with calcification (
Congenital hypoplastic left coronary cusp separated by a membrane-like structure is an extremely rare but noteworthy anomaly.1 This leads to a progressive obstruction of blood flow to the LCA, causing recurrent acute myocardial infarction and sudden death.2 The typical characteristic of coronary angiography and CCTA is a pouch-like filling in the small left sinus of Valsalva, which is an occlusion of the coronary ostium by a rudimentary aortic cusp.3 Patients may experience symptoms of myocardial ischemia, and surgical repair of the coronary ostium is often the only way to treat this anomaly.4
Footnotes
References
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