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Progression of pulmonary veno‐occlusive disease without pulmonary hypertension

Pulmonary veno‐occlusive disease (PVOD) is a progressively fatal disease with no definitive treatment options. PVOD can be a result of genetic mutation but can also be due secondary to exposure to solvents or chemotherapeutic agents. Generally, at the time of diagnosis PVOD is associated with hemody...

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Autores principales: Beshay, Sarah, Humbert, Marc, Barrios, Roberto, Sahay, Sandeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052978/
https://www.ncbi.nlm.nih.gov/pubmed/35506066
http://dx.doi.org/10.1002/pul2.12046
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author Beshay, Sarah
Humbert, Marc
Barrios, Roberto
Sahay, Sandeep
author_facet Beshay, Sarah
Humbert, Marc
Barrios, Roberto
Sahay, Sandeep
author_sort Beshay, Sarah
collection PubMed
description Pulmonary veno‐occlusive disease (PVOD) is a progressively fatal disease with no definitive treatment options. PVOD can be a result of genetic mutation but can also be due secondary to exposure to solvents or chemotherapeutic agents. Generally, at the time of diagnosis PVOD is associated with hemodynamically confirmed pulmonary hypertension (PH). In this study, we describe a patient who was diagnosed with PVOD early in the disease without hemodynamically confirmed PH. She had histologically confirmed PVOD. Her clinical presentation posed management challenges and prednisone therapy was used to stabilize her disease. This case and some recently published reports highlight possible immune dysregulation in PVOD and role for immuno‐suppressive therapy in these patients.
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spelling pubmed-90529782022-05-02 Progression of pulmonary veno‐occlusive disease without pulmonary hypertension Beshay, Sarah Humbert, Marc Barrios, Roberto Sahay, Sandeep Pulm Circ Case Reports Pulmonary veno‐occlusive disease (PVOD) is a progressively fatal disease with no definitive treatment options. PVOD can be a result of genetic mutation but can also be due secondary to exposure to solvents or chemotherapeutic agents. Generally, at the time of diagnosis PVOD is associated with hemodynamically confirmed pulmonary hypertension (PH). In this study, we describe a patient who was diagnosed with PVOD early in the disease without hemodynamically confirmed PH. She had histologically confirmed PVOD. Her clinical presentation posed management challenges and prednisone therapy was used to stabilize her disease. This case and some recently published reports highlight possible immune dysregulation in PVOD and role for immuno‐suppressive therapy in these patients. John Wiley and Sons Inc. 2022-02-21 /pmc/articles/PMC9052978/ /pubmed/35506066 http://dx.doi.org/10.1002/pul2.12046 Text en © 2022 The Authors. Pulmonary Circulation published by John Wiley & Sons Ltd on behalf of Pulmonary Vascular Research Institute. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Beshay, Sarah
Humbert, Marc
Barrios, Roberto
Sahay, Sandeep
Progression of pulmonary veno‐occlusive disease without pulmonary hypertension
title Progression of pulmonary veno‐occlusive disease without pulmonary hypertension
title_full Progression of pulmonary veno‐occlusive disease without pulmonary hypertension
title_fullStr Progression of pulmonary veno‐occlusive disease without pulmonary hypertension
title_full_unstemmed Progression of pulmonary veno‐occlusive disease without pulmonary hypertension
title_short Progression of pulmonary veno‐occlusive disease without pulmonary hypertension
title_sort progression of pulmonary veno‐occlusive disease without pulmonary hypertension
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052978/
https://www.ncbi.nlm.nih.gov/pubmed/35506066
http://dx.doi.org/10.1002/pul2.12046
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