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Isolated pulmonary valve endocarditis with rapid progression: a case report and literature review
BACKGROUND: Isolated pulmonary valve endocarditis (IPE) is rare, accounting for 1.5–2% of all cases of infective endocarditis. Herein, we describe a case of isolated pulmonary valve endocarditis with rapid progression in a 28-year-old male. Unlike most patients reported previously who were cured wit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841888/ https://www.ncbi.nlm.nih.gov/pubmed/33509229 http://dx.doi.org/10.1186/s13019-020-01375-w |
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author | Zhang, Ming-Xuan Zhang, Wei-Min Yu, Chan Zhao, Bo-Wen Chen, Ran Pan, Mei Wang, Bei |
author_facet | Zhang, Ming-Xuan Zhang, Wei-Min Yu, Chan Zhao, Bo-Wen Chen, Ran Pan, Mei Wang, Bei |
author_sort | Zhang, Ming-Xuan |
collection | PubMed |
description | BACKGROUND: Isolated pulmonary valve endocarditis (IPE) is rare, accounting for 1.5–2% of all cases of infective endocarditis. Herein, we describe a case of isolated pulmonary valve endocarditis with rapid progression in a 28-year-old male. Unlike most patients reported previously who were cured with only anti-infective therapy, without surgery at an early stage, multiple complications occurred in this patient in less than 2 weeks. CASE PRESENTATION: The patient was diagnosed with pulmonary valve endocarditis with blood cultures showing Staphylococcus aureus and echocardiography revealing 2 masses (measuring 14*13 mm、11*16 mm in size). Only 12 days later, acute massive pulmonary embolism occurred. Then, repeated echocardiography revealed multiple masses attached to the pulmonary valve with severe pulmonary insufficiency and the possibility of pulmonary valve destruction. Finally, pulmonary valve replacement, vegetation removal, and right pulmonary thromboendarterectomy together with resection of the middle and lower lobes of the right lung were performed. CONCLUSIONS: The role of surgery at an early stage might need to be reconsidered, and it may be viable to combine medical and surgical approaches. |
format | Online Article Text |
id | pubmed-7841888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78418882021-01-28 Isolated pulmonary valve endocarditis with rapid progression: a case report and literature review Zhang, Ming-Xuan Zhang, Wei-Min Yu, Chan Zhao, Bo-Wen Chen, Ran Pan, Mei Wang, Bei J Cardiothorac Surg Case Report BACKGROUND: Isolated pulmonary valve endocarditis (IPE) is rare, accounting for 1.5–2% of all cases of infective endocarditis. Herein, we describe a case of isolated pulmonary valve endocarditis with rapid progression in a 28-year-old male. Unlike most patients reported previously who were cured with only anti-infective therapy, without surgery at an early stage, multiple complications occurred in this patient in less than 2 weeks. CASE PRESENTATION: The patient was diagnosed with pulmonary valve endocarditis with blood cultures showing Staphylococcus aureus and echocardiography revealing 2 masses (measuring 14*13 mm、11*16 mm in size). Only 12 days later, acute massive pulmonary embolism occurred. Then, repeated echocardiography revealed multiple masses attached to the pulmonary valve with severe pulmonary insufficiency and the possibility of pulmonary valve destruction. Finally, pulmonary valve replacement, vegetation removal, and right pulmonary thromboendarterectomy together with resection of the middle and lower lobes of the right lung were performed. CONCLUSIONS: The role of surgery at an early stage might need to be reconsidered, and it may be viable to combine medical and surgical approaches. BioMed Central 2021-01-28 /pmc/articles/PMC7841888/ /pubmed/33509229 http://dx.doi.org/10.1186/s13019-020-01375-w Text en © The Author(s) 2021 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/. 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 in a credit line to the data. |
spellingShingle | Case Report Zhang, Ming-Xuan Zhang, Wei-Min Yu, Chan Zhao, Bo-Wen Chen, Ran Pan, Mei Wang, Bei Isolated pulmonary valve endocarditis with rapid progression: a case report and literature review |
title | Isolated pulmonary valve endocarditis with rapid progression: a case report and literature review |
title_full | Isolated pulmonary valve endocarditis with rapid progression: a case report and literature review |
title_fullStr | Isolated pulmonary valve endocarditis with rapid progression: a case report and literature review |
title_full_unstemmed | Isolated pulmonary valve endocarditis with rapid progression: a case report and literature review |
title_short | Isolated pulmonary valve endocarditis with rapid progression: a case report and literature review |
title_sort | isolated pulmonary valve endocarditis with rapid progression: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841888/ https://www.ncbi.nlm.nih.gov/pubmed/33509229 http://dx.doi.org/10.1186/s13019-020-01375-w |
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