Lung Histopathology Flashcards

1
Q

What is the FEV1:FVC ratio in obstructive lung disease

A

Reduced FEV1:FVC ratio (FEV1 is lower, but FVC remains similar)

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2
Q

Give the site, aetiology and pathology of chronic bronchitis

A

chronic bronchitis

site: bronchus
aetiology: tobacco smoke, pollution
pathology: airway dilation, excessive mucus production

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3
Q

Give the site, aetiology and pathology of bronchiectesis

A

bronchiectesis

site: bronchus
aetiology: inflammatory (e.g. post-infectious, asthma), congential (e.g. CysFib, primary ciliary dyskinesia)
pathology: airway dilation and scarring

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4
Q

Give the site, aetiology and pathology of asthma

A

asthma

site: bronchus
aetiology: immunological: allergens, cold air, exercise, drug interactions
pathology: Inflammation, SM cell hyperplasia, excess mucus production

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5
Q

Give the site, aetiology and pathology of emphysema

A

emphysema

site: acini
aetiology: tobacco smoke, a1-AT defiency (reduced production from tissue degrading enzymes)
pathology: Airspace enlargement (reduced alveolar emptying), wall destruction

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6
Q

Give the site, aetiology and pathology of small airway disease/bronchiolitis

A

small airway disease/bronchiolitis

site: bronchiole
aetiology: tobacco smoke, air pollutants
pathology: inflammatory scarring/obliteration

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7
Q

Give the clinical features, histological features and complications of chronic bronchitis

A

chronic bronchitis
clinical features: cough and sputum on most days in 3 month periods ongoing for over 2 years
histological features: airway dilation, goblet cell hyperplasia, mucus gland hypertrophy
complications: recurrent infections, chronic hypoxia, pulmonary htn

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8
Q

Give the clinical features, histological features and complications of bronchiectesis

A

bronchiectesis
clinical features: cough, purulent sputum, fever
histological features:
complications: recurrent infection, pulmonary htn, haemoptysis, amyloidosis

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9
Q

Give the clinical features, histological features and complications of asthma

A

asthma
clinical features: dyspynoea, wheezing, episodic cough
histological features: eosinophils, curschman spirals (shed epithelium), Charcot-Leyden crystals
complications: Chronic asthma, other atopy, anaphylaxis

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10
Q

Give the clinical features, histological features and complications of emphysema

A

emphysema
clinical features: dyspnoea, cough
histological features: loss of alveolar parenchyma distal to the terminal bronchiole (acinar).
complications: pulmonary htm, pneumothorax, respiratory failure

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11
Q

Name 3 inflammatory and 3 congenital cause of bronchiectesis

A
Inflammatory:
Post infectious (esp kids)
Post-inflammatory (aspiration)
Asthma
Connective tissue diseases
Ciliary dyskineasia (kartageners)
Obstruction 

Congenital
CysFib
Primary ciliary dyskinesia (also inflam)
Hypogammaglobulinemia (also inflam)

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12
Q

What is the FEV1:FVC ratio in interstitial (restrictive) lung disease?

A

Relatively normal ratio, reduced FVC,

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13
Q

Describe 3 features of interstitial lung disease on spirometry

A

restrictive (decreased CO diffusion capacity, decreased lung volume, decreased compliance).

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14
Q

Describe 5 clinical features of interstitial lung disease presentation

A

SOB, End inspiratory crackles, cyanois, pulmonary htn, cor pulmonale

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15
Q

What are the 4 main categories of interstitial lung disease?

A

Fibrosing,
Granulomatous,
Eosinophillic,
Smoking related

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16
Q

What are the 6 types of Fibrosing ILD?

A
Idiopathic pulmonary fibrosis
Pneumoconiosis
Cryptogenic organizing pneumonia
Connective tissue disease associated
Drug induced
Radiation pneumonitis
17
Q

What are the 3 types of granulomatous ILD?

A

Sarcoid
Extrinsic allergic alveolits
Associated with vasculitides (wegeners, churg strauss, microscopic polyangiitis etc.)

18
Q

What histological feature is present in end stage ILD?

A

Honey-combing

makes it difficult to find initial cause in end stage disease.