Cardiac amyloidosis is a progressive disorder and is sometimes difficult to diagnose even when suspected in the appropriate clinical setting. We present an interesting case of rapidly progressive light-chain cardiac amyloidosis and highlights the importance of close monitoring even when the initial biopsy and imaging findings are not pathognomonic for amyloidosis. (Level of Difficulty: Beginner.).
Keywords: AL, light-chain; ATTR, transthyretin; CA, cardiac amyloidosis; CMR, cardiac magnetic resonance; ECV, extracellular volume; MGUS, monoclonal gammopathy of unknown significance; NT-proBNP, N-terminal pro-B-type natriuretic peptide; amyloidosis; biopsy; cardiac magnetic resonance.
© 2020 The Authors.