Interstitial lung disease Flashcards

1
Q

What is an ILD?

A

any disease process affecting the lung interstitial that interferes with gas transfer and has a restrictive lung pattern

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2
Q

What are the symptoms of an ILD?

A

breathlessness and a dry cough

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3
Q

What are the types of ILD?

A
  • idiopathic interstitial pneumonia
  • granulomatous ILDs
  • other
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4
Q

What is pneumoconiosis?

A

lung damage caused by inhalation of mineral dusts by occupational exposure

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5
Q

What are the types of coal workers pneumoconiosis?

A
  • simple doesn’t affect lung function and is associated with COPD
  • complicated is progressive massive fibrosis leading to a restrictive pattern with breathlessness, progressive dyspnoea and a cough with black sputum
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6
Q

What is coal workers pneumoconiosis caused by?

A

exposure to coal dust

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7
Q

What is silicosis caused by?

A

quartz exposure

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8
Q

What is silicosis?

A

upper lobe micro nodular infiltrates and hilar lymphadenopathy with eggshell classification

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9
Q

What is complicated silicosis?

A

micro nodules coalesce to form destructive lung disease similar to massive fibrosis

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10
Q

What is acute silicosis?

A

rapidly progressive alveolar infiltrates

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11
Q

What is different about asbestosis to IPF?

A

asbestosis presents at a younger age than IPF

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12
Q

What three things does asbestos cause?

A
  • pleural disease (benign pleural plaques which are asymptomatic, acute asbestos pleuritic, malignant mesothelioma which is incurable and pleural effusions that can’t be treated)
  • pulmonary fibrosis (asbestosis which is from heavily prolonged exposure)
  • bronchial carcinoma
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13
Q

What is the pathology of early stage ILD?

A

alveolitis leading to fibrosis

exemplified by adult respiratory distress syndrome

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14
Q

What are the causes of ILD?

A
  • environmental: minerals, drugs, radiation

- idiopathic: connective tissue disease or IPF

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15
Q

What are the ways of getting a biopsy of ILD?

A
  • transbronchial (special forceps)

- thoracoscopic (more invasive but more reliable)

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16
Q

What is the pathology of IPF?

A
  • sub pleural and basal fibrosis
  • inflammatory component variable
  • dilated spaces surrounded by fibrous walls
  • therefore, bad gas exchange
17
Q

What is the pathology of sarcoidosis?

A

multisystem granulomas

18
Q

What are the other signs in sarcoidosis?

A
  • uveitis
  • erythema nodosum
  • lymphadenopathy
  • hypercalcemia
19
Q

What is the pathology of hypersensitivity pneumonitis?

A
  • inflammation of small airways
  • spreads to the interstitium
  • occasional granulomas with allergic origin (type 3 and 4 hypersensitivity)
20
Q

What is the pathology of connective tissue disease?

A

interstitial fibrosis, pleural effusions or rheumatoid nodules