Hypersensitivity pneumonitis, also known as extrinsic allergy alveolitis, is an immunologically-indiced lung disease by fine organic dust particles.
Numerous causative substances have been identified:
~10% regularly exposed hosts develop EAA
Acute form: 4-6 hours after intense exposure: fever, chills, malaise, dyspnea, dry cough, lasting 24 hours. Chest X ray is normal or with bilateral mixed interstitial and airspace opacities. ABG show hypoxemia. It is often misdiagnosed as infectious pneumonia.
Subacute: insidious onset cough, sputum, exertional dyspnea, weight loss, fine crackles, PFT restriction and decreased DLCO
Chronic: irreversible disease, progressing to cor pulmonale and respiratory failure. Interstitial fibrosis leads to peripheral opacities on chest X ray. PFT shows mixed reactive and obstructive patterns.
granulmoas suggests type IV hypersensitivity.
abnormalities suggests lymphocytic alveolitis: low CD4+/CD8+
Recognize and avoid antigen exposure.
Wear a SCBA if avoidance is impossible.
Low dose systemic steroids can be used to control symtoms
Chronic hypersensitivity pneumonitis is a serious condition.