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Atrial septal defect with a rare occupying lesion in heart

BACKGROUND: Cardiac epicardium hemangiomas are exceedingly rare; however, they can cause significant hemodynamic impairment and large pericardial effusions. On rare occasion, cardiac tumors coexist with malformations of the heart. CASE PRESENTATION: We present the case of a 10-month-old female infan...

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Autores principales: Chen, Jinlan, Gong, Xueyang, Xie, Li, Wu, Qin, Zhao, Tianli, Hu, Shijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652894/
https://www.ncbi.nlm.nih.gov/pubmed/36371149
http://dx.doi.org/10.1186/s12872-022-02919-9
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author Chen, Jinlan
Gong, Xueyang
Xie, Li
Wu, Qin
Zhao, Tianli
Hu, Shijun
author_facet Chen, Jinlan
Gong, Xueyang
Xie, Li
Wu, Qin
Zhao, Tianli
Hu, Shijun
author_sort Chen, Jinlan
collection PubMed
description BACKGROUND: Cardiac epicardium hemangiomas are exceedingly rare; however, they can cause significant hemodynamic impairment and large pericardial effusions. On rare occasion, cardiac tumors coexist with malformations of the heart. CASE PRESENTATION: We present the case of a 10-month-old female infant with a rare cardiac surface hemangioma coexisting with malformations of the heart. It revealed an atrial septal defect (ASD) coexisting with an abnormal occupying lesion with high echogenicity. It was 35*12*9 mm in size and was found in the anterior atrioventricular junction to the posterior atrioventricular junction at the bottom of the ventricular septum by transthoracic echocardiography. We performed surgical treatment of the atrial septal defect and performed biopsy with the occupying lesion. The histopathological examination reported a benign tumor as hemangioma. As far as we know, this is the first case in which cardiac surface hemangioma was found to coexist with an atrial septal defect. CONCLUSIONS: Cardiac epicardium hemangiomas is a rare solid tumor of the heart. If the mass is impossible to resect and does not cause hemodynamic impairment, only mass biopsy is possible.
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spelling pubmed-96528942022-11-15 Atrial septal defect with a rare occupying lesion in heart Chen, Jinlan Gong, Xueyang Xie, Li Wu, Qin Zhao, Tianli Hu, Shijun BMC Cardiovasc Disord Case Report BACKGROUND: Cardiac epicardium hemangiomas are exceedingly rare; however, they can cause significant hemodynamic impairment and large pericardial effusions. On rare occasion, cardiac tumors coexist with malformations of the heart. CASE PRESENTATION: We present the case of a 10-month-old female infant with a rare cardiac surface hemangioma coexisting with malformations of the heart. It revealed an atrial septal defect (ASD) coexisting with an abnormal occupying lesion with high echogenicity. It was 35*12*9 mm in size and was found in the anterior atrioventricular junction to the posterior atrioventricular junction at the bottom of the ventricular septum by transthoracic echocardiography. We performed surgical treatment of the atrial septal defect and performed biopsy with the occupying lesion. The histopathological examination reported a benign tumor as hemangioma. As far as we know, this is the first case in which cardiac surface hemangioma was found to coexist with an atrial septal defect. CONCLUSIONS: Cardiac epicardium hemangiomas is a rare solid tumor of the heart. If the mass is impossible to resect and does not cause hemodynamic impairment, only mass biopsy is possible. BioMed Central 2022-11-12 /pmc/articles/PMC9652894/ /pubmed/36371149 http://dx.doi.org/10.1186/s12872-022-02919-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Chen, Jinlan
Gong, Xueyang
Xie, Li
Wu, Qin
Zhao, Tianli
Hu, Shijun
Atrial septal defect with a rare occupying lesion in heart
title Atrial septal defect with a rare occupying lesion in heart
title_full Atrial septal defect with a rare occupying lesion in heart
title_fullStr Atrial septal defect with a rare occupying lesion in heart
title_full_unstemmed Atrial septal defect with a rare occupying lesion in heart
title_short Atrial septal defect with a rare occupying lesion in heart
title_sort atrial septal defect with a rare occupying lesion in heart
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652894/
https://www.ncbi.nlm.nih.gov/pubmed/36371149
http://dx.doi.org/10.1186/s12872-022-02919-9
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