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Idiopathic pulmonary fibrosis

Evidence: Unconfirmed

Names

Idiopathic pulmonary fibrosis
Interstitial pulmonary fibrosis
Interstitial pneumonia
Cryptogenic organizing pneumonia (subtype)

Description

Idiopathic pulmonary fibrosis is a scaring of the lungs. It is suspected that the scaring is due to an autoinflammatory or autoimmune response. However, there are other causes, and only a fraction of patients with IPF suffer from an autoimmune form of the disease.

Bloggers

None found

Prevalence

US Cases: 660,000 - 1,500,000 [Raghu 2014]. It is not known if all of these cases are autoimmune.

Typical Age of onset

No specific age

Symptoms

  • Clubbed fingers (tips of fingers become noticeably swollen or enlarged)

  • Shortness of breath

  • Dry cough