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usual interstitial pneumonia (UIP)


aka: idiopathic pulmonary fibrosis (IPF)
  • 5-6th decade; M:F = 1:1
  • clubbing of fingers (83%)
  • monocytosis/lymphocytosis on lavage
  • increased occurence of bronchogenic CA
  • average survival of 4-6 years; 87% mortality

CXR findings:
  • occasional ground glass pattern in early stage of alveolitis
  • diffuse reticulations (60%) predominantly at bases
  • honeycombing
  • pleural effusion (4%); pleural thickening (6%)
  • pneumothorax in 7% (late stage)
  • progressive volume loss

HRCT findings:

  • basilar predominance, subpleural distribution
  • ground glass infiltrates in active disease
  • septal thickening and distortion
  • honeycombing
  • traction bronchiectasis

see: interstitial pulmonary fibrosis


Yong H. Hahn, MD  -  2 February 1995
Last updated:  1 October 2013


 

Related CHORUS documents:
interstitial pulmonary fibrosis
Hamman-Rich syndrome
rheumatoid lung disease
drugs toxic to lung
cavitary lung nodules
esophagus: scleroderma

 

Copyright © 2013, Charles E. Kahn, Jr.