Cargando…
Lung fibrosis in autoimmune diseases and hypersensitivity: how to separate these from idiopathic pulmonary fibrosis
Lung involvement in autoimmune diseases (AID) is uncommon, but may precede other organ manifestations. A diagnostic problem is chronicity presenting with lung fibrosis. A new category of interstitial pneumonia with autoimmune features for patients with clinical symptoms of AID and presenting with us...
Autores principales: | Popper, Helmut, Stacher-Priehse, Elvira, Brcic, Luka, Nerlich, Andreas |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287245/ https://www.ncbi.nlm.nih.gov/pubmed/34605934 http://dx.doi.org/10.1007/s00296-021-05002-2 |
Ejemplares similares
-
Advanced interstitial lung fibrosis with emphysema and pulmonary
hypertension with no evidence for interstitial lung disease on high resolution
CT
por: Foris, Vasile, et al.
Publicado: (2019) -
Distribution and prognostic significance of gluconeogenesis and glycolysis in lung cancer
por: Smolle, Elisabeth, et al.
Publicado: (2020) -
Senescence and autophagy in usual interstitial pneumonia of different etiology
por: Gallob, Florian, et al.
Publicado: (2020) -
Direct medical costs of hospitalized patients with idiopathic pulmonary fibrosis in a tertiary hospital in China
por: Zheng, Xiao-Fen, et al.
Publicado: (2020) -
Idiopathic Pulmonary Fibrosis Update: Reconciliation with Hypersensitivity Pneumonitis Guidelines Required?
por: Moran-Mendoza, Onofre
Publicado: (2022)