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A rare case of severe right heart failure due to pulmonary artery lymphomatoid granulomatosis
Lymphomatoid granulomatosis is a rare, vascular‐centric, and vessel‐destroying lymphoproliferative disease that hardly involves the pulmonary arteries. Herein, we report a case with severe right heart failure and pulmonary arterial stenosis caused by pulmonary artery lymphomatoid granulomatosis. Thi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754766/ https://www.ncbi.nlm.nih.gov/pubmed/32964628 http://dx.doi.org/10.1002/ehf2.13000 |
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author | Su, Hongling Wei, Rong Duan, Yichao Guo, Zhaoxia Wang, Aqian Jiang, Na Li, Wanpeng Zhu, Yan Guo, Yanqing Zhang, Min Zhang, Yan Cao, Yunshan |
author_facet | Su, Hongling Wei, Rong Duan, Yichao Guo, Zhaoxia Wang, Aqian Jiang, Na Li, Wanpeng Zhu, Yan Guo, Yanqing Zhang, Min Zhang, Yan Cao, Yunshan |
author_sort | Su, Hongling |
collection | PubMed |
description | Lymphomatoid granulomatosis is a rare, vascular‐centric, and vessel‐destroying lymphoproliferative disease that hardly involves the pulmonary arteries. Herein, we report a case with severe right heart failure and pulmonary arterial stenosis caused by pulmonary artery lymphomatoid granulomatosis. This case was diagnosed by percutaneous transluminal pulmonary artery biopsy and was effectively treated with stent implantation and steroid administration. |
format | Online Article Text |
id | pubmed-7754766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77547662020-12-23 A rare case of severe right heart failure due to pulmonary artery lymphomatoid granulomatosis Su, Hongling Wei, Rong Duan, Yichao Guo, Zhaoxia Wang, Aqian Jiang, Na Li, Wanpeng Zhu, Yan Guo, Yanqing Zhang, Min Zhang, Yan Cao, Yunshan ESC Heart Fail Case Reports Lymphomatoid granulomatosis is a rare, vascular‐centric, and vessel‐destroying lymphoproliferative disease that hardly involves the pulmonary arteries. Herein, we report a case with severe right heart failure and pulmonary arterial stenosis caused by pulmonary artery lymphomatoid granulomatosis. This case was diagnosed by percutaneous transluminal pulmonary artery biopsy and was effectively treated with stent implantation and steroid administration. John Wiley and Sons Inc. 2020-09-10 /pmc/articles/PMC7754766/ /pubmed/32964628 http://dx.doi.org/10.1002/ehf2.13000 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Su, Hongling Wei, Rong Duan, Yichao Guo, Zhaoxia Wang, Aqian Jiang, Na Li, Wanpeng Zhu, Yan Guo, Yanqing Zhang, Min Zhang, Yan Cao, Yunshan A rare case of severe right heart failure due to pulmonary artery lymphomatoid granulomatosis |
title | A rare case of severe right heart failure due to pulmonary artery lymphomatoid granulomatosis |
title_full | A rare case of severe right heart failure due to pulmonary artery lymphomatoid granulomatosis |
title_fullStr | A rare case of severe right heart failure due to pulmonary artery lymphomatoid granulomatosis |
title_full_unstemmed | A rare case of severe right heart failure due to pulmonary artery lymphomatoid granulomatosis |
title_short | A rare case of severe right heart failure due to pulmonary artery lymphomatoid granulomatosis |
title_sort | rare case of severe right heart failure due to pulmonary artery lymphomatoid granulomatosis |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754766/ https://www.ncbi.nlm.nih.gov/pubmed/32964628 http://dx.doi.org/10.1002/ehf2.13000 |
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