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Functional Intracardiac Paraganglioma

A 39-year-old man presented to the department of emergency medicine in Seoul National University Hospital complaining of chest pain, heart palpitation, and headache. Upon arrival, a computed tomography scan showed a 7.0 cm×6.2 cm lesion with the typical features of a paraganglioma. The patient was t...

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Detalles Bibliográficos
Autores principales: Chung, Yongwoo, Choi, Jae Woong, Kim, Kyung-Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Thoracic and Cardiovascular Surgery 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155182/
https://www.ncbi.nlm.nih.gov/pubmed/32309209
http://dx.doi.org/10.5090/kjtcs.2020.53.2.86
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author Chung, Yongwoo
Choi, Jae Woong
Kim, Kyung-Hwan
author_facet Chung, Yongwoo
Choi, Jae Woong
Kim, Kyung-Hwan
author_sort Chung, Yongwoo
collection PubMed
description A 39-year-old man presented to the department of emergency medicine in Seoul National University Hospital complaining of chest pain, heart palpitation, and headache. Upon arrival, a computed tomography scan showed a 7.0 cm×6.2 cm lesion with the typical features of a paraganglioma. The patient was treated with an alpha-blocker and a beta-blocker prior to surgical intervention. We removed the tumor successfully, and histopathologic findings indicated that the tumor was indeed a paraganglioma. Since intracardiac paraganglioma is a rare disease, we present this case together with a literature review.
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spelling pubmed-71551822020-04-17 Functional Intracardiac Paraganglioma Chung, Yongwoo Choi, Jae Woong Kim, Kyung-Hwan Korean J Thorac Cardiovasc Surg Case Report A 39-year-old man presented to the department of emergency medicine in Seoul National University Hospital complaining of chest pain, heart palpitation, and headache. Upon arrival, a computed tomography scan showed a 7.0 cm×6.2 cm lesion with the typical features of a paraganglioma. The patient was treated with an alpha-blocker and a beta-blocker prior to surgical intervention. We removed the tumor successfully, and histopathologic findings indicated that the tumor was indeed a paraganglioma. Since intracardiac paraganglioma is a rare disease, we present this case together with a literature review. The Korean Society for Thoracic and Cardiovascular Surgery 2020-04-05 2020-04-05 /pmc/articles/PMC7155182/ /pubmed/32309209 http://dx.doi.org/10.5090/kjtcs.2020.53.2.86 Text en Copyright © The Korean Society for Thoracic and Cardiovascular Surgery. 2020. All right reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Chung, Yongwoo
Choi, Jae Woong
Kim, Kyung-Hwan
Functional Intracardiac Paraganglioma
title Functional Intracardiac Paraganglioma
title_full Functional Intracardiac Paraganglioma
title_fullStr Functional Intracardiac Paraganglioma
title_full_unstemmed Functional Intracardiac Paraganglioma
title_short Functional Intracardiac Paraganglioma
title_sort functional intracardiac paraganglioma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155182/
https://www.ncbi.nlm.nih.gov/pubmed/32309209
http://dx.doi.org/10.5090/kjtcs.2020.53.2.86
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