The clinical case of cardiac pseudoamyloidosis associated with multiple myeloma

The clinical case of cardiac pseudoamyloidosis associated with multiple myeloma Cardiac amyloidosis is an infiltrative cardiomyopathy resulting from extracellular deposition amyloid- a specific protein-polysaccharide complex. This demonstrates unverified amyloid-like heart lesion in the presence unexplained thickening wall undilated left ventricle and manifestations restrictive failure patient myeloma. difficulty establishing accurate diagnosis lies existence large number types amyloidogenic proteins, diversity picture, absence pathognomonic symptoms single non-invasive diagnostic tool for verification.