79 year old female
Dyspnea


-
- CT PA (Expiration
- GGO’s
- pulmonary edema
- small airway disease
- GGO’s
- CT PA (Expiration

Air trapping
Moaic Attenuation
- 9 months ago
- PFTs-
FEV1 1.79 (96%)
FVC 2.36 (95%)
FEV1/FVC 1.0
FEF25-75 89%, BDR 61% (false-elevated due to low FVC?)
TLC 88%
RV 73%
FRC not measured
ERV 55%
DLCO 82%
VA not measured
DLCO/VA 148%
Flow volume loop normal
IC/VC >85%
- PFTs-
- 7 months ago
- Hi Res
- Small airway disease
- basilar airway thickening
- bronchiolectasis
- air trapping
- GGO’s
- reticular changes
- Small airway disease
- Hi Res

Basilar small airway disease, ground glass , reticular changes and bronchiolectasis, mosaic attenuation

Basilar small airway disease, ground glass , reticular changes and bronchiolectasis, mosaic attenuation

Basilar small airway disease, ground glass , reticular changes and bronchiolectasis, mosaic attenuation

Basilar small airway disease, ground glass , reticular changes and bronchiolectasis, mosaic attenuation

Centrilobular nodule

reticular changes
bronchiolectasis

Air trapping not significantly different from inspiration image
-
- Bronchoscopy
- Normal Airways
- Echo Normal
- Bronchoscopy
- Elevated ESR 46
CT 3 months ago
Persistent but improved areas of groundglass opacification, air
trapping and mild dependent subpleural reticulations. Differential
includes small airways/small vessel disease and hypersensitivity
pneumonitis.

Improved but persistent GGO reticular changes and bronchiolectasis

Improved but persistent GGO reticular changes and bronchiolectasis

Improved but persistent GGO reticular changes and bronchiolectasis

Improved but persistent GGO reticular changes and bronchiolectasis
Path
1 month ago
RIGHT LOWER LOBE LUNG CRYOBIOPSY
Airway-centered fibrosis, peribronchiolar metaplasia, and mild chronic inflammation with occasional giant cell.
No lymphoid aggregates, germinal centers, or dominant plasmacytosis seen (lymphocytes > plasma cells).
No acute inflammation or foreign material observed.
Note: The pattern of inflammation raises the histologic differential of fibrotic hypersensitivity pneumonitis, however other airway-centered fibrosing disorders could also be considered. Clinical and radiologic correlation is advised. Exclusion of UIP
among other ILD’s cannot be entirely excluded due to sampling method.