Interstitial Lung Disease Flashcards
What are the different categories of diffuse lung disease?
Drug induced Granulomatous Other Idiopathic interstitial pneumonitis: =- Usual interstitial pneumonia/IPF = Nonspecific interstitial pneumonia = Cryptogenic organising pneumonia = AIP, RBILD, DIP, LIP
Common cause of granulomatous lung disease?
Sarcoidosis
–> nodular lung infiltrates in mid and upper zones
Mediastinal and hilar LAD
What is pLAM?
Lymphangioleiomyomatosis
Premenopausal female esp. tuberous sclerosis
–> cystic lung disease
What is COP?
Consolidation in lower zones + ground glass changes + pulmonary nodules + pleural thickening
Granulation + fibrin + collagen
Caused by connective tissue diseases, drugs and as a post infective complication
Rare ILD significant features?
DIP = smoking related - stop smoking –> resolution
AIP = ARDS equivalent = hyaline membrane
NSIP features
Bilateral patchy and subpleural areas of ground glass in the lower zones
NO HONEYCOMBING
Temporal distribution of changes
UIP features
High mortality at 2 yrs
Predominantly Male ex smokers
Present with progressive SOB
HONEYCOMBING
Temporal heterogeneity
Refer for lung transplant
Treat with prednisone
New treatments = Pirfenidone and nintedanib