Interstitial Lung Disease Flashcards

1
Q

What are the different categories of diffuse lung disease?

A
Drug induced
Granulomatous
Other
Idiopathic interstitial pneumonitis:
 =- Usual interstitial pneumonia/IPF
= Nonspecific interstitial pneumonia
= Cryptogenic organising pneumonia
= AIP, RBILD, DIP, LIP
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2
Q

Common cause of granulomatous lung disease?

A

Sarcoidosis

–> nodular lung infiltrates in mid and upper zones
Mediastinal and hilar LAD

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3
Q

What is pLAM?

A

Lymphangioleiomyomatosis
Premenopausal female esp. tuberous sclerosis
–> cystic lung disease

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4
Q

What is COP?

A

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

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5
Q

Rare ILD significant features?

A

DIP = smoking related - stop smoking –> resolution

AIP = ARDS equivalent = hyaline membrane

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6
Q

NSIP features

A

Bilateral patchy and subpleural areas of ground glass in the lower zones
NO HONEYCOMBING
Temporal distribution of changes

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7
Q

UIP features

A

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

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