Lung Pathology Flashcards

1
Q

Name obstructive lung disease

A
  • Chronic bronchitis
  • Bronchiectasis
  • Asthma
  • Emphysema
  • Small airway disease/bronchiolitis
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2
Q

Describe the site, pathology, aetiology, clinical features, histological features, and complications of chronic bronchitis

A

Site
- Bronchus

Pathology

  • Dilatation of airways
  • Excess mucus production

Aetiology

  • Tobacco smoking
  • Air pollution

Clinical features

  • Cough and sputum
  • Most days for 3 months
  • For 2 years

Histological features

  • Dilatation of the airways
  • Hyperplasia of goblet cells
  • Hypertrophy of mucous glands

Complications

  • Recurrent infections
  • Chronic hypoxia
  • Pulmonary hypertension
  • Lung cancer
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3
Q

Describe the site, pathology, aetiology, clinical features, histological features, and complications of bronchiectasis

A

Site
- Bronchus

Pathology
- Airway dilatation and scarring

Aetiology

  • Infection
  • Cystic fibrosis

Clinical features

  • Cough
  • Sputum production
  • Scarring

Histological features
- Permanent dilatation of bronchi

Complications

  • Recurrent infections
  • haemoptysis
  • Pulmonary hypertension
  • Amyloidosis
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4
Q

Describe the site, pathology, aetiology, clinical features, histological features, and complications of asthma

A

Site
- Bronchus

Pathology

  • Smooth muscle hyperplasia
  • Excess mucus
  • Inflammation
  • IgE mediated

Aetiology:

  • Atopic march
  • Hypersensitivity reaction
  • Allergens and exertion

Clinical features

  • Cough and wheeze
  • Episodic
  • Night cough

Histological features
- Eosinophils

Complications

  • Chronic asthma
  • Death
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5
Q

Describe the site, pathology, aetiology, clinical features, histological features, and complications of emphysema

A

Site
- Acinus

Pathology

  • Airspace enlargement
  • Alveolar wall destruction

Aetiology

  • Tobacco smoking
  • Alpha 1 antitrypsin deficiency

Clinical features

  • Dyspnoea
  • Cough

Histological features
- Loss of alveolar spaces

Complications

  • Bullae
  • Pneumothorax
  • Pulmonary hypertension
  • Respiratory failure
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6
Q

List some causes of bronchiectasis

A

Inflammatory:

  • Post-infectious
  • Obstruction
  • Systemic disease
  • Asthma

Congenital:

  • Cystic fibrosis
  • Amongst others
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7
Q

Describe interstitial lung disease

A

Diseases of the pulmonary connective tissue which usually show a restrictive picture of lung disease.

Categorised into:
- Fibrosing (pulmonary fibrosis, pneumoconiosis, drug-induced)
- Granulomatous (sarcoidosis, TB, 
vasculitides)
- Eosinophilic
- Smoking related
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8
Q

Describe idiopathic pulmonary fibrosis

A

This more commonly affects males and shows a fibrotic pattern or honeycomb changes to the lung. There are a variety of potential causes and it presents with dyspnoea, a non productive cough and a expiratory fine crackle. It usually presents at 40-70 years of age.

It is treated with steroids but this has little impact on prognosis.

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9
Q

What is pneumoconiosis?

A

An occupational lung disease, usually affecting the upper lobe.

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10
Q

Describe granulomatous lung disease

A

A granuloma is a collection of macrophages and infections include TB, fungus and others. Non-infectious causes include sarcoidosis and occupational lung disease.

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11
Q

What is extrinsic allergic alveolitis

A

An immune mediated disorder caused by exposure to antigens. It presents acutely with systemic symptoms that usually settle within a day. Examples:

  • Farmer’s lung (mouldy hay)
  • Pigeon fancier’s lung (feathers)
  • Humidifier’s lung (heated water systems)
  • Malt-worker’s lung (barley)
  • Cheese washer’s lung mouldy cheese)
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12
Q

What are the different tumours of the lung?

A

Non-small cell cancers:

  • Adenocarcinomas
  • Squamous cell carcinomas
  • Large cell carcinomas

Small cell cancers

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13
Q

Describe squamous cell cancers of the lung

A

These represent up to 50% of lung cancers.

This usually affects males and is closely correlated with smoking. It is usually found at the bronchi and locally spreads but metastasises late. There are a variety of types but they all tend to evolve as a result of epithelial damage and metaplasia into squamous cells.

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14
Q

Describe adenocarcinomas

A

These represent up to 30% of lung cancers

They are most common in women and non-smokers and are malignant cells with glandular differentiation and mucin production. They are usually peripheral tumours and they metastasise early.

They are associated with EGFR mutations.

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15
Q

Describe large cell lung cancer

A

These are poorly differentiated tumours with very poor prognosis.

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16
Q

Describe small cell lung cancer

A

These usually occur centrally and usually arise from neuroendocrine cells. They divide rapidly and therefore metastasise early and have poor prognosis.

They are usually associated with paraneoplastic syndromes according to the hormone the tumour secretes (ACTH, ADH, PTH, calcitonin, serotonin, bradykinin)

17
Q

How are lung cancers staged?

A

TNM staging

  • Tumour size and invasion (T1-4)
  • Node involvement (N0-2)
  • Metastasis (M0-1)
18
Q

Describe pulmonary embolism

A
  • 95% will originate from DVTs
  • Risk factors: female, OCP, immobility, pregnancy
  • Virchow’s triad
  • Large can cause death
  • Small can be silent but recurrent can cause pulmonary hypertension
  • Non-thrombotic: amniotic fluid, air, fat, bone marrow
19
Q

Describe pulmonary hypertension

A

A mean pulmonary arterial pressure of >25mmHg and it is classified according to aetiology:

  • Class 1: primary
  • Class 2: left cardiac failure
  • Class 3: lung disease
  • Class 4: thromboembolic
  • Class 5: unclear multifactorial mechanisms

Pathophysiology:
Can be pre-capillary, capillary, post capillary, causing a build up of pressure.

It complicates into right sided cardiac failure

20
Q

Describe pulmonary oedema

A
  • Poor gas exchange

- Usually caused by left sided heart failure

21
Q

Describe diffuse alveolar damage

A

In adults:

  • Acute respiratory distress syndrome
  • Infection, trauma, aspiration etc.
  • 40% mortality
  • Can resolve completely
  • Sometimes has residual scarring

In neonates:

  • Hyaline membrane disease
  • Insufficient surfactant production

Lungs are expanded and plum coloured
Airless lungs