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Vanishing lung syndrome Masquerading as bilateral pneumothorax: A case report

Vanishing lung syndrome (VLS) is a rare condition characterized by giant emphysematous bullae. It is frequently misdiagnosed as pneumothorax. We describe a case of a 30-year-old male who presented with shortness of breath, reduced effort tolerance, and pleuritic chest pain for three months. He was i...

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Autores principales: Muhamad, Nur Izat, Mohd Nawi, Siti Nurbaya, Yusoff, Bazli Md, Ab Halim, Noor Azizah, Mohammad, Nurashikin, Wan Ghazali, Wan Syamimee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658491/
https://www.ncbi.nlm.nih.gov/pubmed/33209576
http://dx.doi.org/10.1016/j.rmcr.2020.101276
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author Muhamad, Nur Izat
Mohd Nawi, Siti Nurbaya
Yusoff, Bazli Md
Ab Halim, Noor Azizah
Mohammad, Nurashikin
Wan Ghazali, Wan Syamimee
author_facet Muhamad, Nur Izat
Mohd Nawi, Siti Nurbaya
Yusoff, Bazli Md
Ab Halim, Noor Azizah
Mohammad, Nurashikin
Wan Ghazali, Wan Syamimee
author_sort Muhamad, Nur Izat
collection PubMed
description Vanishing lung syndrome (VLS) is a rare condition characterized by giant emphysematous bullae. It is frequently misdiagnosed as pneumothorax. We describe a case of a 30-year-old male who presented with shortness of breath, reduced effort tolerance, and pleuritic chest pain for three months. He was initially diagnosed with bilateral pneumothorax based on clinical examination and chest radiograph findings. However, further imaging with a high resolution computed tomography (HRCT) of the thorax confirmed bilateral giant emphysematous bullae. Our patient subsequently underwent video-assisted thoracoscopic surgery (VATS) and bullectomy. In this report, we discuss the clinical presentations, radiological features, and the management of VLS. We also highlight the differentiating features of VLS from a pneumothorax.
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spelling pubmed-76584912020-11-17 Vanishing lung syndrome Masquerading as bilateral pneumothorax: A case report Muhamad, Nur Izat Mohd Nawi, Siti Nurbaya Yusoff, Bazli Md Ab Halim, Noor Azizah Mohammad, Nurashikin Wan Ghazali, Wan Syamimee Respir Med Case Rep Case Report Vanishing lung syndrome (VLS) is a rare condition characterized by giant emphysematous bullae. It is frequently misdiagnosed as pneumothorax. We describe a case of a 30-year-old male who presented with shortness of breath, reduced effort tolerance, and pleuritic chest pain for three months. He was initially diagnosed with bilateral pneumothorax based on clinical examination and chest radiograph findings. However, further imaging with a high resolution computed tomography (HRCT) of the thorax confirmed bilateral giant emphysematous bullae. Our patient subsequently underwent video-assisted thoracoscopic surgery (VATS) and bullectomy. In this report, we discuss the clinical presentations, radiological features, and the management of VLS. We also highlight the differentiating features of VLS from a pneumothorax. Elsevier 2020-11-06 /pmc/articles/PMC7658491/ /pubmed/33209576 http://dx.doi.org/10.1016/j.rmcr.2020.101276 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Muhamad, Nur Izat
Mohd Nawi, Siti Nurbaya
Yusoff, Bazli Md
Ab Halim, Noor Azizah
Mohammad, Nurashikin
Wan Ghazali, Wan Syamimee
Vanishing lung syndrome Masquerading as bilateral pneumothorax: A case report
title Vanishing lung syndrome Masquerading as bilateral pneumothorax: A case report
title_full Vanishing lung syndrome Masquerading as bilateral pneumothorax: A case report
title_fullStr Vanishing lung syndrome Masquerading as bilateral pneumothorax: A case report
title_full_unstemmed Vanishing lung syndrome Masquerading as bilateral pneumothorax: A case report
title_short Vanishing lung syndrome Masquerading as bilateral pneumothorax: A case report
title_sort vanishing lung syndrome masquerading as bilateral pneumothorax: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658491/
https://www.ncbi.nlm.nih.gov/pubmed/33209576
http://dx.doi.org/10.1016/j.rmcr.2020.101276
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