| Literature DB >> 23231421 |
Candida Cristina Quarta1, Laura Obici, Pier Luigi Guidalotti, Maurizio Pieroni, Simone Longhi, Stefano Perlini, Laura Verga, Giampaolo Merlini, Claudio Rapezzi.
Abstract
Amyloidotic cardiomyopathy is still a widely underdiagnosed condition that usually requires endomyocardial biopsy (EMB) for a definite diagnosis. 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid (99mTc-DPD) has proven highly sensitive for detecting amyloidotic cardiomyopathy due to transthyretin-related amyloid deposition. Herein we report the first description of the (99mTc-DPD scintigraphy profile in a patient with suspected amyloidotic cardiomyopathy and a final EMB- and genetically-proven diagnosis of familial apolipoprotein AI amyloidosis due to Leu174Ser variant.Entities:
Mesh:
Substances:
Year: 2012 PMID: 23231421 DOI: 10.3109/13506129.2012.746938
Source DB: PubMed Journal: Amyloid ISSN: 1350-6129 Impact factor: 7.141