Please use this identifier to cite or link to this item:
https://www.um.edu.mt/library/oar/handle/123456789/82181
Title: | Spontaneous pneumomediastinum in idiopathic pulmonary fibrosis |
Authors: | Conti, Luca Bilocca, David Gouder, Caroline Montefort, Stephen |
Keywords: | Mediastinal emphysema Idiopathic pulmonary fibrosis Pulmonary fibrosis -- Case studies Lungs -- Diseases -- Diagnosis |
Issue Date: | 2021-10 |
Publisher: | University of Malta. Medical School |
Citation: | Conti, L., Bilocca, D., Gouder, C., & Montefort, S. (2021). Spontaneous pneumomediastinum in idiopathic pulmonary fibrosis. Malta Medical Journal, 33(2), 107-110. |
Abstract: | Spontaneous pneumomediastinum is an uncommon occurrence and is usually self-limiting. Spontaneous pneumomediastinum is the presence of free air around mediastinal structures and is thought to be secondary to alveolar or honeycomb cyst rupture due to raised intrapulmonary pressure on coughing, blunt force trauma to the chest, asthma, various types of interstitial lung diseases, including interstitial pneumonia associated with connective tissue diseases, including dermatomyositis and rheumatoid arthritis. We herein report a rare case of spontaneous pneumomediastinum with thoracic-wall subcutaneous emphysema occurring in an elderly gentleman with idiopathic pulmonary fibrosis (IPF). |
URI: | https://www.um.edu.mt/library/oar/handle/123456789/82181 |
Appears in Collections: | MMJ, Volume 33, Issue 2 MMJ, Volume 33, Issue 2 |
Files in This Item:
File | Description | Size | Format | |
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MMJ33(2)CR1.pdf | 358.57 kB | Adobe PDF | View/Open |
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