Hypersensitivity pneumonitis

Key Facts
  • Chest usually normal in acute, subacute disease
  • Midlung fibrosis in chronic disease
  • HRCT: centrilobular ground glass nodules with air trapping
  • Usually spares costophrenic angles
  • Allergic reaction organic antigens especially thermophilic actinomycetes
  • Nonspecific flu like symptoms
  • Often misdiagnosed as “pneumonia’
Imaging Findings

Chest Radiograph

  • Often normal especially acute and subacute forms
  • Miliary disease
  • Chronic: midlung to upper lung zone fibrosis, bronchiectasis, and volume loss
  • No pleural disease or adenopathy

CT/HRCT

  • More sensitive but may be normal
  • Ground glass centrilobular nodules acutely
  • Most prominent med to lower lungs
  • Air trapping common
  • Spares costophrenic angles
Differential Diagnosis
  • Idiopathic pulmonary fibrosis
  • Eosinophilic granuloma
  • Sarcoid
  • Pneumoconiosis
  • Scleroderma
  • Differentiation
    • IPF does not spare costophrenic angles
    • EG nodules may cavitate
    • Patients with EG smoke, smoking less common in hypersensitivity pneumonitis
    • Sarcoid peribronchovascular distribution
    • Pneumoconiosis: dust history, may have adenopathy
    • Scleroderma, dilated esophagus
Pathological Features
  • Airborne organic particles (1-5 um)
  • Thermophilic actinomycetes
  • Exposure
    • Farmer’s lung
    • Pigeon breeders lung
    • Humidifier lung
  • Loosley formed noncaseating granulomas
  • Lymphocytic infiltration
  • BOOP
Clinical Presentation
  • Acute, subacute, chronic forms, considerable overlap
  • Nonspecific symptoms
  • Often mistaken as pneumonia
    • Patient removed from environment
    • Gets well with antibiotic treatment
  • Cough, dyspnea, fever 4-6 hours following exposure
  • Individual must be susceptible (allergic response), most dust exposed individuals have no response
  • Treatment
    • Removal from environment
    • Steroids
References

Lynch DA, Newell JD, Logan PM, et al. Can CT distinguish hypersensitivity pneumonitis from idiopathic pulmonary fibrosis? AJR 165:807-811, 1995
Matar LD, McAdams HP , Sporn TA. Hypersensitivity pneumonitis AJR 174:1061-1066, 2000