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Primary pulmonary angiosarcoma: Three case reports and literature review
Primary pulmonary angiosarcoma is a rare type of malignant vascular tumor with a very aggressive clinical course and a grim prognosis. To date, only a handful of cases have been reported in English literature. Its rarity and consequent low index of suspicion makes clinical diagnosis difficult. In th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5193014/ https://www.ncbi.nlm.nih.gov/pubmed/27766785 http://dx.doi.org/10.1111/1759-7714.12376 |
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author | Ren, Yanhong Zhu, Min Liu, Yan Diao, Xiaoli Zhang, Yuhui |
author_facet | Ren, Yanhong Zhu, Min Liu, Yan Diao, Xiaoli Zhang, Yuhui |
author_sort | Ren, Yanhong |
collection | PubMed |
description | Primary pulmonary angiosarcoma is a rare type of malignant vascular tumor with a very aggressive clinical course and a grim prognosis. To date, only a handful of cases have been reported in English literature. Its rarity and consequent low index of suspicion makes clinical diagnosis difficult. In this report we present three cases of primary pulmonary angiosarcoma with cough, hemoptysis, and progressive dyspnea to contribute to the sparse literature on this disease. A review is made of previous reports of primary pulmonary angiosarcomas, and the clinical characteristics, diagnosed method, treatment options, and prognosis of pulmonary angiosarcoma are also discussed. |
format | Online Article Text |
id | pubmed-5193014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51930142016-12-29 Primary pulmonary angiosarcoma: Three case reports and literature review Ren, Yanhong Zhu, Min Liu, Yan Diao, Xiaoli Zhang, Yuhui Thorac Cancer Case Reports Primary pulmonary angiosarcoma is a rare type of malignant vascular tumor with a very aggressive clinical course and a grim prognosis. To date, only a handful of cases have been reported in English literature. Its rarity and consequent low index of suspicion makes clinical diagnosis difficult. In this report we present three cases of primary pulmonary angiosarcoma with cough, hemoptysis, and progressive dyspnea to contribute to the sparse literature on this disease. A review is made of previous reports of primary pulmonary angiosarcomas, and the clinical characteristics, diagnosed method, treatment options, and prognosis of pulmonary angiosarcoma are also discussed. John Wiley & Sons Australia, Ltd 2016-07-28 2016-09 /pmc/articles/PMC5193014/ /pubmed/27766785 http://dx.doi.org/10.1111/1759-7714.12376 Text en © 2016 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://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 Ren, Yanhong Zhu, Min Liu, Yan Diao, Xiaoli Zhang, Yuhui Primary pulmonary angiosarcoma: Three case reports and literature review |
title | Primary pulmonary angiosarcoma: Three case reports and literature review |
title_full | Primary pulmonary angiosarcoma: Three case reports and literature review |
title_fullStr | Primary pulmonary angiosarcoma: Three case reports and literature review |
title_full_unstemmed | Primary pulmonary angiosarcoma: Three case reports and literature review |
title_short | Primary pulmonary angiosarcoma: Three case reports and literature review |
title_sort | primary pulmonary angiosarcoma: three case reports and literature review |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5193014/ https://www.ncbi.nlm.nih.gov/pubmed/27766785 http://dx.doi.org/10.1111/1759-7714.12376 |
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