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"Usual" interstitial pneumonia with autoimmune features: a prospective study on a cohort of idiopathic pulmonary fibrosis patients.

Gianluca Sambataro,Chiara A Ferrara,Sebastiano E Torrisi,Carla Spadaro,Giovanna Vignigni,Ada Vancheri,Nicoletta Del Papa,Martina Orlandi,Michele Colaci,Lorenzo Malatino,Stefano Palmucci,Lorenzo Cavagna,Domenico Sambataro,Carlo Vancheri

Clinical and experimental rheumatology（2022）

Cited 7|Views3
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Abstract
The association between a single clinical or serological domain of IPAF and UIP pattern is predictive for the development of a SAD if compared with isolated UIP. ILD can be the first manifestation of SAD, even with a UIP pattern, therefore, the morphological domain of IPAF criteria could be removed.
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Key words
interstitial pneumonia with autoimmune features,idiopathic pulmonary fibrosis,usual interstitial pneumonia,undifferentiated connective tissue disease,diagnosis
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