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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Published in: | Frontiers in cardiovascular medicine Vol. 11; p. 1323492 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Switzerland
Frontiers Media S.A
13-02-2024
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Subjects: | |
Online Access: | Get full text |
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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. |
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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 |