The diagnostic challenge of cardiomyopathies: When should we suspect cardiac amyloidosis?
J Nucl Cardiol
.
2020 Oct;27(5):1844-1849.
doi: 10.1007/s12350-019-01922-6.
Epub 2019 Oct 28.
Authors
Magali Gobbo
1
2
,
Daniel Bender
3
,
Hugo Mosto
4
,
Héctor Sueiro
5
,
Andrea Mocskos
5
,
Rita Tepper
3
,
Justo Carbajales
3
Affiliations
1
Department of Nuclear Cardiology, Ramos Mejía Hospital, General Urquiza 609, 1221, Buenos Aires, Argentina. magali_gobbo@hotmail.com.
2
Cardiovascular Institute of Buenos Aires, Buenos Aires, Argentina. magali_gobbo@hotmail.com.
3
Department of Cardiology, Ramos Mejía Hospital, General Urquiza 609, 1221, Buenos Aires, Argentina.
4
Department of Echocardiography, Ramos Mejía Hospital, General Urquiza 609, 1221, Buenos Aires, Argentina.
5
Department of Nuclear Cardiology, Ramos Mejía Hospital, General Urquiza 609, 1221, Buenos Aires, Argentina.
PMID:
31659698
DOI:
10.1007/s12350-019-01922-6
No abstract available
Publication types
Case Reports
MeSH terms
Aged
Amyloidosis / complications*
Amyloidosis / diagnostic imaging*
Cardiomyopathies / diagnostic imaging*
Cardiomyopathies / etiology*
Echocardiography
Humans
Male
Tomography, Emission-Computed, Single-Photon