fibrotic non-specific interstitial pneumonia

Fibrotic non-specific interstitial pneumonitis is a histological subtype of non-specific interstitial pneumonitis (NSIP). It is considered the more common form . This pattern manifests as chronic interstitial inflammation obscured by interstitial fibrosis (with dense collagen), a temporal homogeneous pattern, and occasional focal honeycomb fibrosis .
Treatment and prognosis
Corticosteroid can be given but it carries a worse prognosis than the cellular type.
Differential diagnosis
The key imaging differential is a UIP pattern
- according to one study 62% of patients with UIP showed subpleural predominance whereas 55% of patients with fibrotic NSIP exhibited random distribution