Epicardial cardiac cavernous Haemangioma-a case report

Abstract 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 la...

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Main Authors: Mahmoud Yousef Ibrahim Abuharb, Xiao Ming Bian, Jian He
Format: Article
Language:English
Published: BMC 2019-07-01
Series:BMC Cardiovascular Disorders
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12872-019-1156-6
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author Mahmoud Yousef Ibrahim Abuharb
Xiao Ming Bian
Jian He
author_facet Mahmoud Yousef Ibrahim Abuharb
Xiao Ming Bian
Jian He
author_sort Mahmoud Yousef Ibrahim Abuharb
collection DOAJ
description Abstract 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 doaj.art-84aebeaaeee74c5bb492acdbacc791362022-12-21T18:03:47ZengBMCBMC Cardiovascular Disorders1471-22612019-07-011911510.1186/s12872-019-1156-6Epicardial cardiac cavernous Haemangioma-a case reportMahmoud Yousef Ibrahim Abuharb0Xiao Ming Bian1Jian He2The first affiliated hospital of Dalian Medical UniversityThe first affiliated hospital of Dalian Medical UniversityThe first affiliated hospital of Dalian Medical UniversityAbstract 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.http://link.springer.com/article/10.1186/s12872-019-1156-6Heart neoplasmsHaemangiomaMitral stenosisRheumatic heart
spellingShingle Mahmoud Yousef Ibrahim Abuharb
Xiao Ming Bian
Jian He
Epicardial cardiac cavernous Haemangioma-a case report
BMC Cardiovascular Disorders
Heart neoplasms
Haemangioma
Mitral stenosis
Rheumatic heart
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 Heart neoplasms
Haemangioma
Mitral stenosis
Rheumatic heart
url http://link.springer.com/article/10.1186/s12872-019-1156-6
work_keys_str_mv AT mahmoudyousefibrahimabuharb epicardialcardiaccavernoushaemangiomaacasereport
AT xiaomingbian epicardialcardiaccavernoushaemangiomaacasereport
AT jianhe epicardialcardiaccavernoushaemangiomaacasereport