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USUAL INTERSTITIAL PNEUMONIA (UIP)

“ The UIP pattern is seen with idiopathic pulmonary fibrosis (IPF; the clinical syndrome). It typically affects those >50 years of ag e,...

The UIP pattern is seen with idiopathic pulmonary fibrosis (IPF; the clinical syndrome). It typically affects those >50 years of age, often with a smoking history. The UIP pattern is also seen with rheumatoid lung, systemic sclerosis (can have UIP or non-specific interstitial pneumonia [NSIP] pattern), asbestosis and other connective tissue diseases. Response to steroids and prognosis is poor in IPF.
Plain film
•  Normal at first, then decreased lung volumes with sub-pleural, basal reticulation.
HRCT

•  The classic trio is: 

(1) apicobasal gradient of 
(2) sub-pleural reticular opacities, and 
(3) macrocystic honeycombing and traction bronchiectasis.
•  Ground-glass attenuation less extensive than the reticular opacities.
•  Check for an irregular pleural surface.
•  Typically, abnormal lung is seen next to normal lung.
•  The pattern is typical, biopsy may not be required for diagnosis.
•  10% of IPF patients develop lung cancer.