Article Text
Abstract
Cardiac amyloidosis (CA) describes the pathological process of amyloid protein deposition in the extracellular space of the myocardium. Unfortunately, the diagnosis of CA is often made late and when the disease process is advanced. However, advances in cardiovascular imaging have allowed for better prognostication and establishing diagnostic pathways with high sensitivity and specificity. This review discusses the role of echocardiography, cardiac MRI and nuclear cardiology in current clinical practice for diagnosis and prognosis of CA.
- cardiac amyloidosis
- global longitudinal strain
- cardiomyopathy restrictive
- cardiac mri
- cardio-oncology
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Footnotes
Contributors JL-M planned the manuscript. JL-M, AMA and PP developed the manuscript. JL-M, SH, AMA, PP, AG, CAI, PYK, JBD, NLP and GG helped draft the manuscript. JL-M submitted the manuscript and is responsible as guarantor.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement No additional data are available.