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

Aviat Space Environ Med. 2008 Jul;79(7):704-6. doi: 10.3357/asem.2224.2008.

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.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Aerospace Medicine
  • Humans
  • Lung / diagnostic imaging
  • Male
  • Military Personnel*
  • Pneumothorax / diagnostic imaging
  • Pneumothorax / etiology*
  • Pulmonary Emphysema / etiology
  • Radiography
  • alpha 1-Antitrypsin Deficiency / complications
  • alpha 1-Antitrypsin Deficiency / diagnosis*