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Epicardial cardiac cavernous Haemangioma-a case report

BACKGROUND: Cardiac haemangiomas are exceptionally rare. They are usually solitary growths. Cardiac haemangiomas can be classified as capillary, cavernous, or arteriovenous in nature. They can occur in any chambers of the heart, but are predominantly found at the intramural or endocardial layers. CA...

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Autores principales: Abuharb, Mahmoud Yousef Ibrahim, Bian, Xiao Ming, He, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6664696/
https://www.ncbi.nlm.nih.gov/pubmed/31357944
http://dx.doi.org/10.1186/s12872-019-1156-6
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author Abuharb, Mahmoud Yousef Ibrahim
Bian, Xiao Ming
He, Jian
author_facet Abuharb, Mahmoud Yousef Ibrahim
Bian, Xiao Ming
He, Jian
author_sort Abuharb, Mahmoud Yousef Ibrahim
collection PubMed
description BACKGROUND: Cardiac haemangiomas are exceptionally rare. They are usually solitary growths. Cardiac haemangiomas can be classified as capillary, cavernous, or arteriovenous in nature. They can occur in any chambers of the heart, but are predominantly found at the intramural or endocardial layers. CASE PRESENTATION: This is a rare case of a cardiac haemangioma located on the epicardium of a 52-year-old male patient. The patient complained of 1-year duration of chest tightness and shortness of breath. The haemangioma was removed successfully. For symptomatic lesions, surgical removal remains the preferred treatment. CONCLUSION: The pathological diagnosis was primary cardiac cavernous haemangioma. In this case, the haemangioma was successfully resected with invasive surgery. No recurrence was detected on follow up.
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spelling pubmed-66646962019-08-05 Epicardial cardiac cavernous Haemangioma-a case report Abuharb, Mahmoud Yousef Ibrahim Bian, Xiao Ming He, Jian BMC Cardiovasc Disord Case Report BACKGROUND: Cardiac haemangiomas are exceptionally rare. They are usually solitary growths. Cardiac haemangiomas can be classified as capillary, cavernous, or arteriovenous in nature. They can occur in any chambers of the heart, but are predominantly found at the intramural or endocardial layers. CASE PRESENTATION: This is a rare case of a cardiac haemangioma located on the epicardium of a 52-year-old male patient. The patient complained of 1-year duration of chest tightness and shortness of breath. The haemangioma was removed successfully. For symptomatic lesions, surgical removal remains the preferred treatment. CONCLUSION: The pathological diagnosis was primary cardiac cavernous haemangioma. In this case, the haemangioma was successfully resected with invasive surgery. No recurrence was detected on follow up. BioMed Central 2019-07-29 /pmc/articles/PMC6664696/ /pubmed/31357944 http://dx.doi.org/10.1186/s12872-019-1156-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Abuharb, Mahmoud Yousef Ibrahim
Bian, Xiao Ming
He, Jian
Epicardial cardiac cavernous Haemangioma-a case report
title Epicardial cardiac cavernous Haemangioma-a case report
title_full Epicardial cardiac cavernous Haemangioma-a case report
title_fullStr Epicardial cardiac cavernous Haemangioma-a case report
title_full_unstemmed Epicardial cardiac cavernous Haemangioma-a case report
title_short Epicardial cardiac cavernous Haemangioma-a case report
title_sort epicardial cardiac cavernous haemangioma-a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6664696/
https://www.ncbi.nlm.nih.gov/pubmed/31357944
http://dx.doi.org/10.1186/s12872-019-1156-6
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