Interstitial lung disease Flashcards

1
Q

Sarcoidosis

A

Non-caseating granuloma in lung interstition
Unknown origin
Type 4 hypersensitivity reaction

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2
Q

Hypersensitivity pneumonitis

A

Inflammation of the alveoli within the lung caused by hypersensitivity to inhaled organic dusts
Type 3 hypersensitivity reaction

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3
Q

Treatment for chronic sarcoidosis

A

Oral steroids

Immunosuppression

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4
Q

Treatment for extrinsic allergic alveolitis

A

Oxygen
Steroid
Antigen avoidance

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5
Q

Idiopathic pulmonary fibrosis

A

Imbalance of fibrotic repair system

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6
Q

Pulmonary function test for hypersensitivity pneumonitis

A

Low FEV1 and FVC
High or normal ratio
Low gas transfer

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7
Q

PFT for IPF

A

Low FEV1 and FVC
High or normal ratio
Low gas transfer
Reduced lung volume

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8
Q

Pathology of Idiopathic Pulmonary Fibrosis

A

Usual Interstitial Pneumonia pattern (UIP)
Heterogenous fibrosis in alveolar walls with fibroblastic foci and destruction of architecture causing honeycombing. Inflammation is minimal.

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9
Q

Treatment for IPF

A

Anti-fibrotic drugs

Lung transplant

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10
Q

Simple pneumoconiosis

A

Occupational lung disease

Chest X-ray abnormality-calcification of hilar nodes

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11
Q

Caplan’s syndrome

A

Rheumatoid pneumoconiosis

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12
Q

Silicosis

A

15-20 years exposure to quartz

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13
Q

Chronic/ complicated pneumoconiosis

A

Restrictive pattern

Pulmonary fibrosis

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14
Q

Asbestos related lung disorders

A
Benign pleural plaques
Acute asbestos pleuritis
Pleural effusion and diffuse pleural thickening
Malignant mesothelioma
Bronchial carcinoma
Pulmonary fibrosis (asbestosis)
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15
Q

Early stage interstitial lung disease

A

Alveolitis

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16
Q

What characterises late stage alveolitis

A

Fibrosis

17
Q

What characterises early stage ILD

A

Injury with inflammatory cell infiltration

18
Q

Clinical effects of ILD

A

Hypoxia (respiratory failure) and cardiac failure

19
Q

Transbronchial biopsy

A

Special forceps used at bronchoscopy

20
Q

Thoracoscopic biopsy

A

More invasive but more reliable and generates far more tissue

21
Q

Chronic interstitial diseases

A
Idiopathic pulmonary fibrosis
Sarcoidosis
Extrinsic allergic alveolitis
Pneumoconiosis
Connective tissue diseases
22
Q

Idiopathic Pulmonary Fibrosis

A

Progressive interstitial fibrosis of no known cause

Variable associated inflammation

23
Q

Pathology of IPF

A

Subpleural and basal fibrosis
Inflammatory component variable
Terminally lung structure replaced by dilated spaces surrounded by fibrous walls

24
Q

Allergic origin of extrinsic hypersensitivity pneumonitis

A

Type 3 and type 4 hypersensitivity

25
Q

What allergen causes farmer’s lung?

A

Thermophilic bacteria in mouldy hay

26
Q

What allergen causes bird fancier’s lung?

A

Avian proteins

27
Q

What type of allergen causes malt worker’s lung?

A

Fungi

28
Q

Sarcoidosis

A

Multi-system granulomatous disease of unknown cause

29
Q

Other manifestations of sarcoidosis

A

Lymphadenopathy
Uveitis (inflammation of iris)
Erythema nordosum
Hypercalcaemia

30
Q

Pulmonary involvement in connective tissue disease

A

Pleural effusion
Rheumatoid nodules
Interstitial fibrosis

31
Q

Pneumoconiosis

A

Lung disease caused by mineral dust exposure

32
Q

Examples of types of pneumoconiosis

A

Asbestosis
Coal worker’s lung
Silicosis

33
Q

What factors does pneumoconiosis depend on? (4)

A

Particle size
Particle reactivity
Clearance of particle
Host response