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Occult primary pulmonary synovial sarcoma presenting as recurrent spontaneous pneumothorax and explosive progression

Primary pulmonary synovial sarcoma (PPSS) is a relatively rare neoplasm with highly progressive potential. We present an extremely rare case of PPSS presenting as recurrent pneumothorax with bullous lesions. Bullectomy was performed at the local hospital. Unfortunately, the patient was initially mis...

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Autores principales: Guo, Chenglin, Liu, Chengwu, Pu, Qiang, Lin, Feng, Liu, Lunxu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5334290/
https://www.ncbi.nlm.nih.gov/pubmed/27995774
http://dx.doi.org/10.1111/1759-7714.12410
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author Guo, Chenglin
Liu, Chengwu
Pu, Qiang
Lin, Feng
Liu, Lunxu
author_facet Guo, Chenglin
Liu, Chengwu
Pu, Qiang
Lin, Feng
Liu, Lunxu
author_sort Guo, Chenglin
collection PubMed
description Primary pulmonary synovial sarcoma (PPSS) is a relatively rare neoplasm with highly progressive potential. We present an extremely rare case of PPSS presenting as recurrent pneumothorax with bullous lesions. Bullectomy was performed at the local hospital. Unfortunately, the patient was initially misdiagnosed as atypical carcinoid. Although a negative resection margin was obtained during the first surgery and a remedial operation and chemotherapy followed, the patient developed severe disease progression and died soon after. This report demonstrates that PPSS can easily be misdiagnosed and should be seriously considered in the differential diagnosis of pneumothorax.
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spelling pubmed-53342902017-03-06 Occult primary pulmonary synovial sarcoma presenting as recurrent spontaneous pneumothorax and explosive progression Guo, Chenglin Liu, Chengwu Pu, Qiang Lin, Feng Liu, Lunxu Thorac Cancer Case Reports Primary pulmonary synovial sarcoma (PPSS) is a relatively rare neoplasm with highly progressive potential. We present an extremely rare case of PPSS presenting as recurrent pneumothorax with bullous lesions. Bullectomy was performed at the local hospital. Unfortunately, the patient was initially misdiagnosed as atypical carcinoid. Although a negative resection margin was obtained during the first surgery and a remedial operation and chemotherapy followed, the patient developed severe disease progression and died soon after. This report demonstrates that PPSS can easily be misdiagnosed and should be seriously considered in the differential diagnosis of pneumothorax. John Wiley & Sons Australia, Ltd 2016-12-20 2017-03 /pmc/articles/PMC5334290/ /pubmed/27995774 http://dx.doi.org/10.1111/1759-7714.12410 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
Guo, Chenglin
Liu, Chengwu
Pu, Qiang
Lin, Feng
Liu, Lunxu
Occult primary pulmonary synovial sarcoma presenting as recurrent spontaneous pneumothorax and explosive progression
title Occult primary pulmonary synovial sarcoma presenting as recurrent spontaneous pneumothorax and explosive progression
title_full Occult primary pulmonary synovial sarcoma presenting as recurrent spontaneous pneumothorax and explosive progression
title_fullStr Occult primary pulmonary synovial sarcoma presenting as recurrent spontaneous pneumothorax and explosive progression
title_full_unstemmed Occult primary pulmonary synovial sarcoma presenting as recurrent spontaneous pneumothorax and explosive progression
title_short Occult primary pulmonary synovial sarcoma presenting as recurrent spontaneous pneumothorax and explosive progression
title_sort occult primary pulmonary synovial sarcoma presenting as recurrent spontaneous pneumothorax and explosive progression
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5334290/
https://www.ncbi.nlm.nih.gov/pubmed/27995774
http://dx.doi.org/10.1111/1759-7714.12410
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