| Literature DB >> 29259858 |
Alexander Marco Kollikowski1,2, Florian Kahles3, Svetlana Kintsler4, Sandra Hamada3, Sebastian Reith3, Ruth Knüchel4, Christoph Röcken5, Felix Manuel Mottaghy1,6, Nikolaus Marx3, Mathias Burgmaier3.
Abstract
Cardiac transthyretin-related (ATTR) amyloidosis is a severe cardiomyopathy for which therapeutic approaches are currently under development. Because non-invasive imaging techniques such as cardiac magnetic resonance imaging and echocardiography are non-specific, the diagnosis of ATTR amyloidosis is still based on myocardial biopsy. Thus, diagnosis of ATTR amyloidosis is difficult in patients refusing myocardial biopsy. Furthermore, myocardial biopsy does not allow 3D-mapping and quantification of myocardial ATTR amyloid. In this report we describe a 99mTc-DPD-based molecular imaging technique for non-invasive single-step diagnosis, three-dimensional mapping and semiquantification of cardiac ATTR amyloidosis in a patient with suspected amyloid heart disease who initially rejected myocardial biopsy. This report underlines the clinical value of SPECT-based nuclear medicine imaging to enable non-invasive diagnosis of cardiac ATTR amyloidosis, particularly in patients rejecting biopsy.Entities:
Keywords: Cardiac ATTR amyloidosis; amyloid burden; cardiac magnetic resonance imaging; myocardial biopsy; nuclear cardiac imaging; quantification
Year: 2017 PMID: 29259858 PMCID: PMC5735283 DOI: 10.5582/irdr.2017.01065
Source DB: PubMed Journal: Intractable Rare Dis Res ISSN: 2186-3644