- 58F
- First presented 5 years ago
- cough and wheeze
- Strong FH of pulmonary fibrosis
- Lab
- unrevealing serologies
- PFTs
- restriction and
- reduced DLCO
- CT
- interstitial changes on CT.
- Bronchoscopy
- inflammation and
- lymphocytic predominance.
- VATs biospy
- fibrosis and inflammation r
- UIP vs. Chronic hypersensitivity pneumonitis.
- genetic testing with
- no causative identifiable mutation
- (MUC5B polymorphism not checked).
- Rx
- Nintedanib 150 mg daily for 3 years
- stable exertional capacity
- small fluctuations in her PFT
- CT stable
- Images need to be numbered
- Nintedanib 150 mg daily for 3 years
- First presented 5 years ago