Open AccessInterstitial pneumonitis with autoimmune features: 2 case reports and review of literature
Author(s) -
Antonella Laria,
Alfredomaria Lurati,
D. Mazzocchi,
Mariagrazia Marrazza,
Katia Angela Re,
Paola Faggioli,
Antonino Mazzone
Publication year - 2021
Publication title -
beyond rheumatology
Language(s) - English
Resource type - Journals
ISSN - 2612-5110
DOI - 10.4081/br.2020.46
Subject(s) - medicine , connective tissue , interstitial pneumonia , disease , interstitial lung disease , intensive care medicine , pathology , lung
The classification of interstitial pneumonia with autoimmune features (IPAF) is used to categorize patients with an autoimmune substrate and pulmonary interstitial involvement, who do not meet the classification criteria for any specific connective tissue disease. These patients seem to have a better clinical course than patients with IPAF. The diagnosis of IPAF is of paramount importance and a window of opportunity to identify and to treat forms of early onset of pulmonary interstitial disease without any established damage and to recognize incomplete forms of connective diseases preventing complete clinical manifestation.