Benign respiratory pathology Flashcards

1
Q

Asthma definition

A

Chronic inflammatory disorder of the airways, with paroxysmal bronchospasm causing: wheeze, cough, variable bronchoconstriction that is at least partially reversible

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2
Q

Asthma epidemiology

A
  • Extrinsic (atopic)
  • Children and young adults = 33.9% children with wheeze (1 in 10 UK children diagnosed asthma)
  • Adults = 9-15% occupational cause - commonest occupational lung disease
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3
Q

Asthma pathogenesis

A
  • Mucosal inflammation and oedema
  • Mucus plugs in bronchi
  • Hyperinflated lungs
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4
Q

Atopic asthma

A
  • Type 1 hypersensitivity reaction
  • Caused by allergen
  • Can cause centrilobular emphysema when exacerbated
  • Mucous lands hyperplasia
  • Bronchiolar wall smooth muscle hypertrophy
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5
Q

COPD definition

A

two distinct pathological entities

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6
Q

Chronic bronchitis =

A

Cough with sputum for 3 months in 2 consecutive years

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7
Q

Emphysema =

A

caused by chronic bronchitis - abnormal enlargement of alveolar airspaces

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8
Q

COPD epidemiology

A
  • Smokers

- 1 in 20 of >65yrs consult GP per year

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9
Q

Bronchitis pathogenesis

A
  • Cell damage = inflammation = scar, mucus, infection
  • Bronchiole wall thickened or lumen blocked/damaged
  • Mucus gland hyperplasia
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10
Q

Emphysema pathogenesis

A
  • Increased elastase causes alveolar wall loss and decreased contractility = decreased gas exchange
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11
Q

Classification of emphysema

A
  • Centrilobular (centiacinar) – most associated with smoking and coal dust
  • Panlobular (panacinar) - severest lower lobe bases
  • Paraseptal (distal acinar) – can rupture pneumothorax
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12
Q

Key clinical features of COPD

A
  • Dyspnoea
  • Cough: mucus and irritation of lining
  • Sputum: hyperproduction of mucus
  • Infection
  • Right heart signs: increased workload as increased resistance pulmonary HTN and right ventricular hypertrophy
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13
Q

Bronchiectasis definition

A
  • Permanent dilation of bronchi and bronchioles caused by destruction of the muscle and elastic tissue (usually with inflammation)
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14
Q

Bronchiectasis pathogenesis

A

bronchiole damage due to infection or autoimmune conditions = inflammation = wall pulled open by adjacent scar/collapse

  • Scars cause a major abscess complication
  • Bronchiole wall thickened but lumen dilated
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15
Q

Aetiology of Bronchiectasis

A
  • Cystic fibrosis,
  • Primary ciliary dyskinesia,
  • Kartagener syndrome
  • Bronchial obstruction (tumour, foreign body)
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16
Q

Key clinical features of Bronchiectasis

A
  • Cough, fever, copious foul smelling and yellow/green sputum, abscesses
  • Complications = pneumonia, septicaemia, metastatic infection, amyloid (deposits of amyloid in lungs)
17
Q

Interstitial Lung Disease (ILD) definition

A

group of diffuse and chronic diseases of pulmonary connective tissue – may affect alveolar walls/air spaces and bronchioles

18
Q

ILD pathogenesis

A
  • Trigger causes inflammation and fibrosis in bronchioles

- Leads to thickening = decreased lung compliance

19
Q

Key clinical features of acute ILD

A
  • Damage to lung parenchyma causing acute respiratory distress syndrome = respiratory alkalosis
20
Q

Key clinical features of chronic ILD

A
  • Can affect a lot of alveolar tissue before symptoms arise (dyspnoea increasing for months to years), clubbing, fine crackles, dry cough.
  • End stages = honeycomb lung
21
Q

Cystic fibrosis definition

A
  • Inherited multiorgan disorder of epithelial cells affecting fluid secretion in exocrine glands and the epithelial lining of the respiratory, GI and reproductive organs.
22
Q

Cystic fibrosis epidemiology

A
  • Mostly Caucasians; common: 1/25 carrier
23
Q

Cystic fibrosis aetiology

A
  • Mutation in CFTR gene on chromosome 7
24
Q

Cystic fibrosis pathogenesis

A
  • defective CFTR protein means chloride ions can’t be transported out of cells
  • Water can’t follow so mucous becomes sticky and causes bronchioles to become blocked
  • Hyperplasia of mucus secreting glands, severe chronic bronchitis and bronchiectasis, atrophy and fibrosis of exocrine ducts
25
Q

Key clinical features of CF

A
  • Pancreatic problems = atrophy + fibrosis
  • GI problems = meconium ileus
  • Liver problems = plugging of bile canalucili = cirrhosis
  • 95% of males are infertile
26
Q

Treatment of CF

A
  • 41 years median survival in UK – physio, mucolytics, transplants, vitamins