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Partial Congenital Absence of The Pericardium: A Case Report
The complete or the partial absence of pericardium is a rare congenital malformation for which the patients are commonly asymptomatic and the diagnosis is incidental. The absence of the left side of the pericardium is the most common anomaly that is reported in the literature while the complete abse...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Cirurgia Cardiovascular
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852444/ https://www.ncbi.nlm.nih.gov/pubmed/31165613 http://dx.doi.org/10.21470/1678-9741-2018-0357 |
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author | Benameur, Narjes Arous, Younes landolsi, Manel Chenik, Sarra Abdallah, Nejmeddine Ben Kraiem, Tarek |
author_facet | Benameur, Narjes Arous, Younes landolsi, Manel Chenik, Sarra Abdallah, Nejmeddine Ben Kraiem, Tarek |
author_sort | Benameur, Narjes |
collection | PubMed |
description | The complete or the partial absence of pericardium is a rare congenital malformation for which the patients are commonly asymptomatic and the diagnosis is incidental. The absence of the left side of the pericardium is the most common anomaly that is reported in the literature while the complete absence of pericardium or the absence of the right side of the pericardium are uncommon and their criteria are still unrecognized given their rare occurrence in clinical practice. This paper aims to report a case of 19-year-old male with the congenital partial absence of both sides of the pericardium and to highlight the symptoms and the different cardiac imaging modalities used to confirm the diagnosis of this defect. |
format | Online Article Text |
id | pubmed-6852444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Sociedade Brasileira de Cirurgia Cardiovascular |
record_format | MEDLINE/PubMed |
spelling | pubmed-68524442019-11-15 Partial Congenital Absence of The Pericardium: A Case Report Benameur, Narjes Arous, Younes landolsi, Manel Chenik, Sarra Abdallah, Nejmeddine Ben Kraiem, Tarek Braz J Cardiovasc Surg Case Report The complete or the partial absence of pericardium is a rare congenital malformation for which the patients are commonly asymptomatic and the diagnosis is incidental. The absence of the left side of the pericardium is the most common anomaly that is reported in the literature while the complete absence of pericardium or the absence of the right side of the pericardium are uncommon and their criteria are still unrecognized given their rare occurrence in clinical practice. This paper aims to report a case of 19-year-old male with the congenital partial absence of both sides of the pericardium and to highlight the symptoms and the different cardiac imaging modalities used to confirm the diagnosis of this defect. Sociedade Brasileira de Cirurgia Cardiovascular 2019 /pmc/articles/PMC6852444/ /pubmed/31165613 http://dx.doi.org/10.21470/1678-9741-2018-0357 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Benameur, Narjes Arous, Younes landolsi, Manel Chenik, Sarra Abdallah, Nejmeddine Ben Kraiem, Tarek Partial Congenital Absence of The Pericardium: A Case Report |
title | Partial Congenital Absence of The Pericardium: A Case
Report |
title_full | Partial Congenital Absence of The Pericardium: A Case
Report |
title_fullStr | Partial Congenital Absence of The Pericardium: A Case
Report |
title_full_unstemmed | Partial Congenital Absence of The Pericardium: A Case
Report |
title_short | Partial Congenital Absence of The Pericardium: A Case
Report |
title_sort | partial congenital absence of the pericardium: a case
report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852444/ https://www.ncbi.nlm.nih.gov/pubmed/31165613 http://dx.doi.org/10.21470/1678-9741-2018-0357 |
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