Etymology:
Derived from “emphysema,” meaning “inflation” or “swelling.” Refers to air abnormally located within interstitial tissues of the lung.
AKA:
Pulmonary Interstitial Emphysema (PIE).
What is it?
Interstitial emphysema is the presence of air within the interstitial tissues of the lung, including the connective tissue, perivascular, or peribronchial regions.
Caused by:
Mechanical trauma: Overdistension of alveoli leading to rupture, commonly due to:
Barotrauma from positive-pressure ventilation.
Pulmonary contusion.
Infection: Rare, associated with necrotizing infections causing alveolar rupture.
Inflammation/immune: Rare, in settings like eosinophilic lung disease.
Neoplasm: Air entrapment secondary to obstruction or compression by tumor.
Metabolic: Rarely associated with metabolic diseases causing fragility of connective tissue.
Circulatory: Rare, in cases of pulmonary embolism with associated alveolar damage.
Inherited: Rare, seen in congenital conditions like alveolar capillary dysplasia.
Congenital: More common in neonates with surfactant deficiency or structural immaturity.
Other: Idiopathic cases are rare but reported.
Resulting in:
Air tracking into interstitial spaces, leading to potential compression of airways or vasculature.
Impaired gas exchange and respiratory mechanics.
Structural changes:
Alveolar rupture with air leakage into interstitial tissues.
Compression of adjacent lung structures.
Potential pneumothorax or pneumomediastinum.
Pathophysiology:
Increased alveolar pressure causes rupture.
Air escapes into interstitial tissues, spreading along peribronchial and vascular sheaths.
May lead to subcutaneous emphysema or air embolism if severe.
Pathology:
Gross: Air pockets visible in connective tissue.
Microscopic: Air-filled spaces in perivascular and peribronchial tissues.
Diagnosis:
Clinical assessment, radiological findings, and exclusion of other causes of dyspnea or chest pain.