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Spontaneous massive hemopneumothorax: Double trouble with a twist
Spontaneous hemopneumothorax (SHP) is observed in 3%–7% cases of spontaneous pneumothorax where the tear of an adhesion can lead to bleeding with associated hemothorax. This condition has been reported in patients with hemophilia, sarcoidosis, congenital cystic adenomatoid malformation, systemic lup...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427760/ https://www.ncbi.nlm.nih.gov/pubmed/28474658 http://dx.doi.org/10.4103/lungindia.lungindia_6_16 |
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author | Kuriakose, Milta Khanna, Arjun Talwar, Deepak |
author_facet | Kuriakose, Milta Khanna, Arjun Talwar, Deepak |
author_sort | Kuriakose, Milta |
collection | PubMed |
description | Spontaneous hemopneumothorax (SHP) is observed in 3%–7% cases of spontaneous pneumothorax where the tear of an adhesion can lead to bleeding with associated hemothorax. This condition has been reported in patients with hemophilia, sarcoidosis, congenital cystic adenomatoid malformation, systemic lupus erythematosus, etc., Here, we describe an unusual case of acute massive SHP in a 62-year-old male who underwent a percutaneous transluminal coronary angioplasty (PTCA) and presented with worsening dyspnea over the next 3 days. On evaluation, he had a massive hemopneumothorax which was considered to be secondary to the use of anticoagulants during the PTCA procedure. Pleural fluid analysis revealed frank blood and was consistent with the diagnosis of hemothorax. Surprisingly, the pleural fluid cytology revealed malignant cells. As the patient had a normal chest X-ray 3 days ago, thoracoscopic pleural biopsy was taken which confirmed the diagnosis of an epithelioid mesothelioma. Although post-PTCA or mesothelioma-associated hemothorax has been rarely reported, these two conditions have not been associated with SHP. Since the patient had no prior clinicoradiological features of mesothelioma, the procedure, and the anticoagulants probably contributed to the massive and rapid accumulation of blood. The presence of small amount of air added further confusion to the dual etiology and has not been described earlier. |
format | Online Article Text |
id | pubmed-5427760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54277602017-05-26 Spontaneous massive hemopneumothorax: Double trouble with a twist Kuriakose, Milta Khanna, Arjun Talwar, Deepak Lung India Case Report Spontaneous hemopneumothorax (SHP) is observed in 3%–7% cases of spontaneous pneumothorax where the tear of an adhesion can lead to bleeding with associated hemothorax. This condition has been reported in patients with hemophilia, sarcoidosis, congenital cystic adenomatoid malformation, systemic lupus erythematosus, etc., Here, we describe an unusual case of acute massive SHP in a 62-year-old male who underwent a percutaneous transluminal coronary angioplasty (PTCA) and presented with worsening dyspnea over the next 3 days. On evaluation, he had a massive hemopneumothorax which was considered to be secondary to the use of anticoagulants during the PTCA procedure. Pleural fluid analysis revealed frank blood and was consistent with the diagnosis of hemothorax. Surprisingly, the pleural fluid cytology revealed malignant cells. As the patient had a normal chest X-ray 3 days ago, thoracoscopic pleural biopsy was taken which confirmed the diagnosis of an epithelioid mesothelioma. Although post-PTCA or mesothelioma-associated hemothorax has been rarely reported, these two conditions have not been associated with SHP. Since the patient had no prior clinicoradiological features of mesothelioma, the procedure, and the anticoagulants probably contributed to the massive and rapid accumulation of blood. The presence of small amount of air added further confusion to the dual etiology and has not been described earlier. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5427760/ /pubmed/28474658 http://dx.doi.org/10.4103/lungindia.lungindia_6_16 Text en Copyright: © 2017 Indian Chest Society http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Kuriakose, Milta Khanna, Arjun Talwar, Deepak Spontaneous massive hemopneumothorax: Double trouble with a twist |
title | Spontaneous massive hemopneumothorax: Double trouble with a twist |
title_full | Spontaneous massive hemopneumothorax: Double trouble with a twist |
title_fullStr | Spontaneous massive hemopneumothorax: Double trouble with a twist |
title_full_unstemmed | Spontaneous massive hemopneumothorax: Double trouble with a twist |
title_short | Spontaneous massive hemopneumothorax: Double trouble with a twist |
title_sort | spontaneous massive hemopneumothorax: double trouble with a twist |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427760/ https://www.ncbi.nlm.nih.gov/pubmed/28474658 http://dx.doi.org/10.4103/lungindia.lungindia_6_16 |
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