Pneumothorax ex vacuo: Three cases of an uncommon entity.

Lung India

Department of Pulmonary Medicine, Rajagiri Hospital, Aluva, Kochi, Kerala, India.

Published: January 2023

AI Article Synopsis

  • Pneumothorax can be classified as primary, secondary, or caused by trauma and medical procedures, with tube thoracostomy being the common treatment for most cases.
  • Pneumothorax ex vacuo is a rare type that arises from negative pressure in the pleural space, often due to acute lobar collapse, leading to milder symptoms and a different treatment approach.
  • In cases of pneumothorax ex vacuo, tube thoracostomy is ineffective, and treatment focuses on relieving bronchial obstruction; this article discusses three such cases to inform clinicians about their unique presentation and management.

Article Abstract

Pneumothorax is a frequently encountered entity in pulmonary practice and can be primary or secondary. Traumatic and iatrogenic causes also account for a minority of cases presenting to the chest physician. The most common therapeutic intervention done is a tube thoracostomy in all but the mildest of cases. Pneumothorax ex vacuo is a distinctly uncommon entity that differs considerably from the rest of the pneumothorax cases in its pathogenesis, clinical manifestations, radiological findings, and management. Pneumothorax in this entity results from the sucking in of air into the pleural space caused by an exaggerated negative intrapleural pressure, which is most frequently secondary to acute lobar collapse. Symptoms attributable to pneumothorax per se are distinctly mild and the vital aspect of treatment is to relieve the bronchial obstruction. Tube thoracostomy fails to relieve the pneumothorax in such cases and should be avoided. We share three cases of pneumothorax ex vacuo encountered in our institution and alert clinicians of the presentation, radiology, and management of this uncommon condition.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174644PMC
http://dx.doi.org/10.4103/lungindia.lungindia_517_22DOI Listing

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