Austin Health

Title
Pulmonary alveolar proteinosis with an unusual bronchoscopic complication.
Publication Date
2021-10-04
Author(s)
Sweeney, Duncan J
Munsif, Maitri
Pilcher, David
Stirling, Rob G
Leong, Tracy L
Subject
autoimmune disease
interstitial lung disease
pneumothorax
radiology and other imaging
rare lung diseases
Type of document
Journal Article
OrcId
0000-0002-7811-0424
DOI
10.1002/rcr2.856
Abstract
Pulmonary alveolar proteinosis (PAP) is a rare respiratory syndrome, which can be challenging to diagnose given its non-specific presentation and imaging findings. While most primary cases of PAP have an autoimmune basis, the triggers for the disease are uncertain with occupational factors increasingly thought to be important. We report the unusual complication of pneumomediastinum and bilateral pneumothoraces following endobronchial ultrasound-guided transbronchial needle aspirate in the setting of PAP. We discuss the possible physiological mechanisms of this complication, which appears to be more common in conditions with reduced lung compliance.
Link
Citation
Respirology Case Reports 2021; 9(11): e0856
Jornal Title
Respirology Case Reports
ISSN
2051-3380

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