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Pneumothorax is defined as the presence of air in the pleural space due to: a) communication between alveolar spaces and pleura; b) direct or indirect exchange of air between the atmosphere and the pleural space; or c) the presence of gas producing organisms in the pleural space.
From the clinical and etiological standpoint the pneumothorax is classified as: primary spontaneous pneumothorax if occurring without obvious reason or apparent lung disease, secondary spontaneous pneumothorax if due to a well known underlying lung or systemic disease, or as traumatic pneumothorax if it is the result of iatrogenic or non-iatrogenic blunt and/or penetrating chest interventions and injuries.
Primary spontaneous pneumothorax (PSP) is therefore defined as the presence of air in the pleural space without apparent underlying lung disease or trauma. The pathogenesis of PSP is not the same for all events. Most authors believe that the communication of air between the alveolar spaces and the pleura is due to a rupture of subpleural blebs or bullae .
During thoracoscopy or surgery often there are other lesions present, such as inflammatory elastofibrotic layers with increased porosity and areas of disrupted mesothelial cells at the visceral pleura, allowing air leakage into the pleural space [5, 6].
Bullectomy has a recurrence rate of up to 20% without pleurodesis, which may be explained by factors like peripheral airway inflammation due to noxious agents, e.g. tobacco smoke , or exposure to high levels of ozone as discussed by Abul et al. in this issue of Multidisciplinary Respiratory Medicine (pp. 16-19). Hereditary factors , anatomical abnormalities of the bronchial tree, ischemia at the apices of the lungs , low body mass index due to anorexia and other causes of food restriction , Marfan syndrome  as well as increased aluminium plasma concentrations  may also lead to abnormal connective tissue formations (fibrillopathies) predisposing for the occurrence of PSP .
Secondary spontaneous pneumothorax (SSP) is defined as the presence of air in the pleural space as a consequence of clinically apparent underlying lung disease without iatrogenic or other external blunt (barotraumata, etc.) or penetrating chest injuries. Frequent or typical causes of SSP are:
- chronic airway and alveolar diseases: e.g. severe asthma, cystic fibrosis, emphysema, bullae and cysts;
- infectious lung diseases: e.g. pneumonia (Pneumocystis carinii), TB, lung abscess leading to pneumothorax with pleural empyema;
- interstitial lung diseases: e.g. idiopathic fibrosing alveolitis, sarcoidosis, histiocytosis X, lymphangio leiomyomatosis;
- systemic connective tissue diseases: e.g. rheumatoid arthritis, ankylosing spondylitis, scleroderma, Marfan- and Ehlers Danlos-syndrome;
- malignant lung and chest diseases: e.g. bronchial cancer, sarcoma.
SSP has a higher recurrence rate than PSP, up to 80% in cystic fibrosis.
The age-adjusted incidence of PSP is 7.4-18 cases per 100,000 population each year in males and 1.2-6 in females and it occurs typically at rest. A 2nd World War study showed no difference of incidence between royal air force pilots and army soldiers. Therefore, avoiding physical stress and exercise should not be recommended. In contrast loud music as an atmospheric pressure change may be a risk factor for PSP . Tension pneumothorax in PSP is rare. The outpatient treatment for the first event consists in introducing a small chest tube with a one-way valve (Matthys Drain®) followed by pleurodesis in patients at risk for recurrent PSP .
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