Resp Path 1 - Obstructive diseases Flashcards

1
Q

What is the pulmonary acinus

A

The are of lung distal to the terminal bronchiole.

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2
Q

What is the main epithelium in the lung?

A

Pseudostratified ciliated columnar with seromucinous glands

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3
Q

Define obstructive airways disease?

A

A limitation in airflow caused by an increase in resistance due to a complete or partial obstruction.

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4
Q

Main cause and PFT changes in localised obstruction?

A

Tumour and no changes in PFTs

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5
Q

What is the obstructive pattern of PFTs?

A

Decreased vital capacity, decreased PEFR and decreased FEV1/VC (=0.7).

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6
Q

Which conditions are classified as obstructive airway diseases?

A

Chronic bronchitis/emphysema - COPD
Asthma
Bronchiectasis

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7
Q

What is the definition of chronic bronchitis?

A

Persisent productive cough for three months of the year for two years and not attributed to other causes.

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8
Q

What is the definition of emphysema?

A

Lung condition characterised by abnormal permanent enlargement of the airspaces of the acinus with destruction of the walls (elastin) and minimal fibrosis.

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9
Q

What is meant by blue bloater?

A

Hypoxic, cyanotic and hypercapnic appearance of chronic bronchitis patients.

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10
Q

What is meant by pink puffer?

A

Over-ventilating patients due to parenchymal loss, usually well ventilated at rest.

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11
Q

Main 2 pathological processes in chronic bronchitis?

A
  1. ) Mucous hypersecretion beginning in bronchi and trachea due to hypertrophy of mucous-secreting cells and an increase in mucin-secreting goblet cells in the smaller airway stimulated by inflammatory mediators i.e. histamine and IL-3.
  2. ) Inflammation with neutrophil, macrophage and lymphocyte infiltration and accompanying fibrosis.
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12
Q

What can occur as a result of chronic bronchitis?

A

Squamous cell metaplasia/dysplasia/carcinoma.

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13
Q

Main pathological processes of emphysema?

A

1.) Ongoing inflammation with neutrophil, lymphocyte and macrophage infiltration.
2.) Epithelial injury and proteolysis of extracellular matrix caused by cytokines, elastases and oxidants.
3.) Elastin degradation products cause further inflammation.
Cycle continues unless checked by anti-elastases such as alpha 1 antitrypsin.

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14
Q

How does the loss of elastic tissue in the alveloi impact on breating?

A

It reduces radial traction and causes bronchiole collapse during expiration.

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15
Q

How does emphysema appear on x-rays/CT scans?

A

Lung is voluminous

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16
Q

What is a major complication of emphysema?

A

Alveolar wall rupture –> bullae and blebs –> Pneumothorax

17
Q

What are the four classifications of emphysema?

A
  1. ) Centiacinar
  2. ) Panacinar
  3. ) Distal acinar
  4. ) Irregular
18
Q

Describe centriacinar emphysema?

A

Commonest form, smoking-related, involves destruction of respiratory bronchiole at centre of acinus, upper zones are worse affected.

19
Q

Describe panacinar emphysema?

A

Ass. w/ alpha 1 antitrypsin deficiency, affects whole acinus, lower zones worst affected.

20
Q

Describe distal acinar emphysema?

A

Located at the distal edge of the acinus near the pleura, is the underlying lesion in spontaneous pneumothorax.

21
Q

Describe irregular emphysema?

A

Irregular acinar involvement ass w/ scarring, mainly asymptomatic and of little clinical significance.

22
Q

Define bronchial asthma?

A

Episodic reversible bronchospasm du to an exaggerated bronchoconstrictor response to stimuli leading to dyspnoea, wheezing and cough.

23
Q

What causes the wheezing in bronchial asthma?

A

Resistance to airflow in the smaller airways.

24
Q

Classifications of asthma?

A
  1. ) Atopic
  2. ) Non-atopic
  3. ) Drug-induced
  4. ) Occupational.
25
Q

Describe atopic asthma?

A

Commonest, type 1 IgE hypersensitivty reaction, early childhood and family history, ass w/ eczema +/- hay fever, wheel and flare reaction to skin testing.

26
Q

Describe non-atopic asthma?

A

No allergen sensitisation, ass w/ recurrent infection and pollutants, virally or chemically induced inflammation reduces threshold for vagal stimulation by other minor irritants.

27
Q

Describe drug-induced asthma?

A

Aspirin, related to effects on cyclooxygenase pathway.

28
Q

Describe occupational asthma?

A

Related to fumes, gases, chemicals etc, combo of type I and type III hypersensitivity.

29
Q

Give a detailed account of pathogenesis of bronchial atopic asthma?

A
  1. ) Inhaled allergens elicit type 2 helper T cell response.
  2. ) Cytokines favour IgE production and eosinophil recruitment.
  3. ) IgE coats submucosal mast cellswhich on re-exposure to the allergen release granule contents.
  4. ) Early and late phase reactions are induced.
30
Q

Describe the early phase reaction in bronchial atopic asthma?

A

Bronchoconstriction due to supepithelial vagal stimulation, increased mucous production and variable vasodilation.

31
Q

Describe the late phase reaction?

A

Inflammation with eosinophil, netrophils and T cells stimulate a fresh mediator release with epithelial damage.

32
Q

Early and late phase reactions combine to?

A

Occlude bronchioles with thick mucous plugs –> distal overinflation or atelectasis.

33
Q

Repeated inflammation as a result of bronchial asthma can lead to what pathological processes?

A
  1. ) Bronchial SM hypertrophy
  2. ) Increased vascularity
  3. ) Subepithelial collagen thickening
  4. ) Submucosal gland hypertrophy
  5. ) Goblet cell metaplasia.
34
Q

Define bronchiectasis?

A

Irreversible permanent dilation of bronchi and bronchioles.

35
Q

General pathogenesis of bronchiectasis?

A

Destruction of muscle and elastic tissue resulting from a chronic necrotising infection leading to bronchial dilation.

36
Q

Aetiology of bronchiectasis?

A

Severe infection alone, severe infection w/ bronchial obstruction, immunosuppression, CF.

37
Q

Clinical symptoms of bronchiectasis?

A

Chronic cough, fever, copious amounts of foul-smelling sputum.

38
Q

Histology of bronchiectasis?

A

Mucosal ulceration, granulation tissue, mucosa, submucosa, cartilage and muscle destruction, loss of cilia, fibrosis, inflammation, squamous metaplasia.

39
Q

Briefly describe CF?

A

Autosomal recessive condition affecting long arm of chr 7, abnormal NaCl transfer across basolateral membranes –> increased mucous viscosity.