Takotsubo syndrome and atrial myxoma-identifying a new trigger: a case report

Takotsubo syndrome (TTS) is a rare cardiomyopathy, but its prevalence is increasing due to the greater availability of diagnostic tools, whose pathophysiology is unknown; however, the evidence points to an excess of catecholamines that ends up generating cardiac stunning. The cause of excessive symp...

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Bibliographic Details
Published in:Frontiers in cardiovascular medicine Vol. 11; p. 1323492
Main Authors: Velarde-Acosta, Kevin, Sandoval, Robert, Falcón-Quispe, Luis, Anicama Lima, William Efrain, Baltodano-Arellano, Roberto
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 13-02-2024
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Summary:Takotsubo syndrome (TTS) is a rare cardiomyopathy, but its prevalence is increasing due to the greater availability of diagnostic tools, whose pathophysiology is unknown; however, the evidence points to an excess of catecholamines that ends up generating cardiac stunning. The cause of excessive sympathetic discharge is multifactorial, and some tumors may be related to their origin. In this case report, we present a female patient with TTS whose only identified triggering factor was an atrial myxoma, which generated an unusual clinical presentation. Current multimodal diagnostic tools together with the multidisciplinary evaluation of the HeartTeam allowed an accurate diagnosis and an adequate management of the clinical picture.
Bibliography:Ola Abdelkarim, Albert Einstein College of Medicine, United States
Reviewed by: Andrea Sonaglioni, IRCCS MultiMedica, Italy
Roberto Spina, Gosford Hospital, Australia
ORCID Kevin Velarde-Acosta orcid.org/0000-0001-9132-0445 Robert Sandoval orcid.org/0009-0002-0286-0584 Luis Falcón-Quispe orcid.org/0000-0002-7055-2308 William Efrain Anicama Lima orcid.org/0000-0002-4225-8953 Roberto Baltodano-Arellano orcid.org/0000-0002-7538-2125
Edited by: Patricio López-Jaramillo, Universidad de Santander, Colombia
ISSN:2297-055X
2297-055X
DOI:10.3389/fcvm.2024.1323492