Diagnostic and prognostic value of cardiac imaging in amyloidosis.
Cardiac imaging techniques
Echocardiography
Immunoglobulin light-chain amyloidosis
Magnetic resonance imaging
Nuclear imaging
Transthyretin cardiac amyloidosis
Journal
World journal of cardiology
ISSN: 1949-8462
Titre abrégé: World J Cardiol
Pays: United States
ID NLM: 101537090
Informations de publication
Date de publication:
26 Dec 2020
26 Dec 2020
Historique:
received:
25
06
2020
revised:
28
09
2020
accepted:
17
11
2020
entrez:
4
1
2021
pubmed:
5
1
2021
medline:
5
1
2021
Statut:
ppublish
Résumé
Amyloidosis is an infiltrative disease caused by extracellular protein deposition that has accumulated a lot of scientific production in recent years. Different types of amyloidosis can affect the heart. Transthyretin amyloidosis and light chain amyloidosis are the two most common types of cardiac amyloidosis. These entities have a poor prognosis, so accurate diagnostic techniques are imperative for determining an early therapeutic approach. Recent advances in cardiac imaging and diagnostic strategies show that these tools are safe and can avoid the use of invasive diagnostic techniques to histological confirmation, such as endomyocardial biopsy. We performed a review on the diagnostic and prognostic implications of different cardiac imaging techniques in cardiac amyloidosis. We mainly focus on reviewing echocardiography, cardiac magnetic resonance, computed tomography and nuclear imaging techniques and the different safety measurements that can be done with each of them.
Identifiants
pubmed: 33391613
doi: 10.4330/wjc.v12.i12.599
pmc: PMC7754383
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
599-614Informations de copyright
©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved.
Déclaration de conflit d'intérêts
Conflict-of-interest statement: No potential conflicts of interest.
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