Echocardiographic Evaluation of Cardiac Amyloid
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11886-010-0108-7.pdf
Reference28 articles.
1. Dubrey SW, Cha K, Skinner M, et al.: Familial and primary (AL) cardiac amyloidosis: echocardiographically similar diseases with distinctly different clinical outcomes. Heart 1997, 78:74–82.
2. Falk RH, Plehn JF, Deering T, et al.: Sensitivity and specificity of the echocardiographic features of cardiac amyloidosis. Am J Cardiol 1987, 59:418–422.
3. Palka P, Lange A, Donnelly JE, et al.: Doppler tissue echocardiographic features of cardiac amyloidosis. J Am Soc Echocardiogr 2002, 15:1353–1360.
4. Cueto-Garcia L, Reeder GS, Kyle RA, et al.: Echocardiographic findings in systemic amyloidosis: spectrum of cardiac involvement and relation to survival. J Am Coll Cardiol 1985, 6:737–743.
5. • Rapezzi C, Merlini G, Quarta CC, et al.: Systemic cardiac amyloidoses: disease profiles and clinical courses of the 3 main types. Circulation 2009, 120:1203–1212. This is the first study to demonstrate that the echocardiographic findings and clinical course of cardiac amyloid patients are not all the same. AL amyloid, senile amyloid, and hereditary amyloid each cause a different clinical course that is important to realize for management.
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