Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kuriakose, Milta, Khanna, Arjun, Talwar, Deepak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
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
_version_ 1783235686657163264
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
work_keys_str_mv AT kuriakosemilta spontaneousmassivehemopneumothoraxdoubletroublewithatwist
AT khannaarjun spontaneousmassivehemopneumothoraxdoubletroublewithatwist
AT talwardeepak spontaneousmassivehemopneumothoraxdoubletroublewithatwist