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Abstract usual interstitial pneumonia (uip) is characterised by a distinctive morphological and radiological appearance that was considered the pathognomonic hallmark of idiopathic pulmonary fibrosis (ipf). It argues that uip, while historically considered pathognomonic of idiopathic pulmonary fibrosis (ipf), is also seen in other fibrotic interstitial lung diseases and has a similar poor prognosis. Usual interstitial pneumonia (uip) is characterised by a distinctive morphological and radiological appearance that was considered the pathognomonic hallmark of idiopathic pulmonary fibrosis (ipf).
We read with interest the personal view published by selman and colleagues.1 these authors propose that the usual interstitial pneumonia (uip) pattern be considered a single and discrete entity, consolidating primary and secondary causes. This document discusses usual interstitial pneumonia (uip) as a diagnostic entity Per current guidelines issued by the fi american thoracic society (ats), european respiratory society (ers), japanese respiratory society (jrs) and the latin american thoracic society (lats), a pathologic or radiologic diagnosis of uip is required for a clinical diagnosis of ipf12.
Usual interstitial pneumonia (uip) is a histopathologic and radiologic pattern of interstitial lung disease rather than a disease itself.
Ipf is a progressive fibrosing interstitial pneumonia of unknown etiology and the most common idiopathic interstitial pneumonia It occurs predominantly in older males and typically manifests as a uip pattern on hrct of the chest and histopathology. We believe that the unification of uip as a single diagnostic entity has undeniable advantages.
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