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Pulmonary Artery Sarcoma: A Rare Entity
Pulmonary artery sarcomas (PAS) are extremely rare sarcomas of uncertain histogenesis that often mimic pulmonary thromboemboli. This is a report of a 60-year-old female patient who presented with recurrent chest pain and cough. The patient was first diagnosed with pulmonary embolism but she did not...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528857/ https://www.ncbi.nlm.nih.gov/pubmed/26425600 http://dx.doi.org/10.1177/2324709614529416 |
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author | Shomaf, Maha Obeidat, Nathir Al-Fares, Fatin Najjar, Saleh |
author_facet | Shomaf, Maha Obeidat, Nathir Al-Fares, Fatin Najjar, Saleh |
author_sort | Shomaf, Maha |
collection | PubMed |
description | Pulmonary artery sarcomas (PAS) are extremely rare sarcomas of uncertain histogenesis that often mimic pulmonary thromboemboli. This is a report of a 60-year-old female patient who presented with recurrent chest pain and cough. The patient was first diagnosed with pulmonary embolism but she did not improve on anticoagulant therapy. Follow-up imaging studies revealed a mass in the left hilar region extending into the pulmonary trunk and branches of the left pulmonary artery. The tru-cut biopsy revealed an undifferentiated sarcoma. The patient died 10 months after her initial presentation. |
format | Online Article Text |
id | pubmed-4528857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-45288572015-09-30 Pulmonary Artery Sarcoma: A Rare Entity Shomaf, Maha Obeidat, Nathir Al-Fares, Fatin Najjar, Saleh J Investig Med High Impact Case Rep Article Pulmonary artery sarcomas (PAS) are extremely rare sarcomas of uncertain histogenesis that often mimic pulmonary thromboemboli. This is a report of a 60-year-old female patient who presented with recurrent chest pain and cough. The patient was first diagnosed with pulmonary embolism but she did not improve on anticoagulant therapy. Follow-up imaging studies revealed a mass in the left hilar region extending into the pulmonary trunk and branches of the left pulmonary artery. The tru-cut biopsy revealed an undifferentiated sarcoma. The patient died 10 months after her initial presentation. SAGE Publications 2014-04-03 /pmc/articles/PMC4528857/ /pubmed/26425600 http://dx.doi.org/10.1177/2324709614529416 Text en © 2014 American Federation for Medical Research http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution 3.0 License (http://www.creativecommons.org/licenses/by/3.0/) which permits any 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 (http://www.uk.sagepub.com/aboutus/openaccess.htm). |
spellingShingle | Article Shomaf, Maha Obeidat, Nathir Al-Fares, Fatin Najjar, Saleh Pulmonary Artery Sarcoma: A Rare Entity |
title | Pulmonary Artery Sarcoma: A Rare Entity |
title_full | Pulmonary Artery Sarcoma: A Rare Entity |
title_fullStr | Pulmonary Artery Sarcoma: A Rare Entity |
title_full_unstemmed | Pulmonary Artery Sarcoma: A Rare Entity |
title_short | Pulmonary Artery Sarcoma: A Rare Entity |
title_sort | pulmonary artery sarcoma: a rare entity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528857/ https://www.ncbi.nlm.nih.gov/pubmed/26425600 http://dx.doi.org/10.1177/2324709614529416 |
work_keys_str_mv | AT shomafmaha pulmonaryarterysarcomaarareentity AT obeidatnathir pulmonaryarterysarcomaarareentity AT alfaresfatin pulmonaryarterysarcomaarareentity AT najjarsaleh pulmonaryarterysarcomaarareentity |