Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Shomaf, Maha, Obeidat, Nathir, Al-Fares, Fatin, Najjar, Saleh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2014
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
_version_ 1782384716591136768
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