Spontaneous pneumothorax in flight as first manifestation of alpha-1 antitrypsin deficiency

14Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Alpha-1 antitrypsin deficiency is a genetic condition that increases the risk of a variety of conditions including pulmonary emphysema and chronic liver disease. We report on a 33-yr-old male fighter pilot with early-onset pulmonary emphysema with bullae who developed spontaneous pneumothorax during in-flight combat training. A CT scan of his chest after removal of the chest tube showed multiple variably sized bullae and pulmonary cysts scattered throughout both lungs. Serum levels of alpha-1 antitrypsin were markedly decreased. Genetic analyses showed a PI ZZ genotype. Alpha-1 antitrypsin deficiency often goes undiagnosed by flight surgeons, which is a risk to flight safety. Copyright © by the Aerospace Medical Association.

Cite

CITATION STYLE

APA

Lin, Y. C., Chiu, W. K., Chang, H., Cheng, Y. L., & Chen, J. C. (2008). Spontaneous pneumothorax in flight as first manifestation of alpha-1 antitrypsin deficiency. Aviation Space and Environmental Medicine, 79(7), 704–706. https://doi.org/10.3357/ASEM.2224.2008

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free