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Progressive fibrosing interstitial lung disease: prevalence and clinical outcome.

Byoung Soo KwonJooae ChoeEun Jin ChaeHee Sang HwangYong-Gil KimJin Woo Song
Published in: Respiratory research (2021)
Our results showed that approximately 34% of patients with non-IPF fibrosing ILD showed a progressive phenotype and a poor outcome similar to that of IPF, regardless of the diagnostic criteria used.
Keyphrases
  • interstitial lung disease
  • idiopathic pulmonary fibrosis
  • multiple sclerosis
  • systemic sclerosis
  • risk factors
  • rheumatoid arthritis