Restrictive cardiomyopathy with Isolated Cardiac Amyloidosis: a rarecase
AbstractRestrictive cardiomyopathy is rare and usually associated with
myocardium amyloidosis, which often involves multiple organs. Here, we
describe a rare case of restrictive cardiomyopathy with myocardium
amyloidosis. The diagnosis was established using electrocardiogram,
transthoracic echocardiography, and confirmed using cardiac magnetic
resonance imaging. Nevertheless, no evidence of involvement of the other
organs was observed.