Features of Hypertrophic Cardiomyopathy Danya L. Dinwoodey, MD , Martha Skinner, MD , Martin S. Maron, MD , Ravin Davidoff, MB, BCh , Frederick L. Ruberg, MD Received 20 September 2007; received in revised form 21 October 2007; accepted 21 October 2007. published online 03 January 2008. Abstract Full Text PDF Images References Supplemental Materials Hypertrophic cardiomyopathy and cardiac amyloidosis result in thickening of the left ventricle, as visualized by 2-dimensional echocardiography. Hemodynamically, hypertrophic cardiomyopathy can be typified by a left ventricular outflow tract gradient and systolic anterior motion of the mitral apparatus, findings rarely seen in cardiac amyloidosis. This case series reports 4 patients with cardiac light-chain amyloidosis and left ventricular outflow tract obstruction at rest, suggesting that there may be echocardiographic overlap between these 2 disparate disease processes. In a series of consecutive patients with cardiac light-chain amyloidosis over a 2- year period, the prevalence of these echocardiographic findings was approximately 4%. In conclusion, awareness of this overlap in echocardiographic presentation may permit more accurate diagnosis, particularly at early stages of amyloid disease, when more treatment options exist.
Independent Predictors of Survival in Primary Systemic (AL) Amyloidosis Including Cardiac Biomarkers and Left Ventricular Strain Imaging An Observational Cohort Study