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Primary Pulmonary Artery Sarcoma Confined to the Left Pulmonary Artery

Primary pulmonary artery sarcomas (PPAS) are extremely rare tumors that are often mislabeled as pulmonary emboli (PE). PPAS usually involve the pulmonary trunk and are histologically classified as leiomyosarcoma, spindle cells sarcoma, fibrous histiocytoma, or undifferentiated sarcoma. Our case invo...

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Detalles Bibliográficos
Autores principales: Altshuler, Ellery, Lowther, Grant, Jantz, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113362/
https://www.ncbi.nlm.nih.gov/pubmed/33969719
http://dx.doi.org/10.1177/23247096211014687
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author Altshuler, Ellery
Lowther, Grant
Jantz, Michael
author_facet Altshuler, Ellery
Lowther, Grant
Jantz, Michael
author_sort Altshuler, Ellery
collection PubMed
description Primary pulmonary artery sarcomas (PPAS) are extremely rare tumors that are often mislabeled as pulmonary emboli (PE). PPAS usually involve the pulmonary trunk and are histologically classified as leiomyosarcoma, spindle cells sarcoma, fibrous histiocytoma, or undifferentiated sarcoma. Our case involved a 78-year-old man with an undifferentiated PPAS confined to the left pulmonary artery that was initially misdiagnosed as a PE. After a month-long delay in treatment in which the patient was prescribed warfarin, the correct diagnosis was made. Pulmonary artery endarterectomy and left lung pneumonectomy were performed, and he survived for 18 months before disease recurrence and death. Our case helps illustrate some of the clinical and radiographic findings that help distinguish PPAS from PE.
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spelling pubmed-81133622021-05-13 Primary Pulmonary Artery Sarcoma Confined to the Left Pulmonary Artery Altshuler, Ellery Lowther, Grant Jantz, Michael J Investig Med High Impact Case Rep Case Report Primary pulmonary artery sarcomas (PPAS) are extremely rare tumors that are often mislabeled as pulmonary emboli (PE). PPAS usually involve the pulmonary trunk and are histologically classified as leiomyosarcoma, spindle cells sarcoma, fibrous histiocytoma, or undifferentiated sarcoma. Our case involved a 78-year-old man with an undifferentiated PPAS confined to the left pulmonary artery that was initially misdiagnosed as a PE. After a month-long delay in treatment in which the patient was prescribed warfarin, the correct diagnosis was made. Pulmonary artery endarterectomy and left lung pneumonectomy were performed, and he survived for 18 months before disease recurrence and death. Our case helps illustrate some of the clinical and radiographic findings that help distinguish PPAS from PE. SAGE Publications 2021-05-10 /pmc/articles/PMC8113362/ /pubmed/33969719 http://dx.doi.org/10.1177/23247096211014687 Text en © 2021 American Federation for Medical Research https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Altshuler, Ellery
Lowther, Grant
Jantz, Michael
Primary Pulmonary Artery Sarcoma Confined to the Left Pulmonary Artery
title Primary Pulmonary Artery Sarcoma Confined to the Left Pulmonary Artery
title_full Primary Pulmonary Artery Sarcoma Confined to the Left Pulmonary Artery
title_fullStr Primary Pulmonary Artery Sarcoma Confined to the Left Pulmonary Artery
title_full_unstemmed Primary Pulmonary Artery Sarcoma Confined to the Left Pulmonary Artery
title_short Primary Pulmonary Artery Sarcoma Confined to the Left Pulmonary Artery
title_sort primary pulmonary artery sarcoma confined to the left pulmonary artery
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113362/
https://www.ncbi.nlm.nih.gov/pubmed/33969719
http://dx.doi.org/10.1177/23247096211014687
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