Chapter 8b Flashcards

1
Q

What are diffuse parenchymal lung diseases?

A

Group of lung diseases characterised by widespread inflammatory pathology, predominantly in the interstitium

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are two consequences of diffuse parenchymal lung diseases?

A
  1. Reduced compliance of lungs - edema and fibrosis of alveolar walls renders them rigid
  2. Thickening of alveolar walls also results in reduced gas exchange
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are 4 histological patterns of reaction in the lung following damage?

A

Hemorrhage and fibrin exudation into alveoli

Edema and inflammation of interstitium

Macrophage accumulation in alveolar spaces

Fibrosis in interstitium or alveolar spaces

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the pathophysiology of ARDS?

A
  1. Damaging Stimulus to Lung
  2. Damage to alveolar lining cells (pneumocytes) & damage to alveolar capillary endothelium (pulmonary endothelium)
  3. Interstitial edema & protein exudation into alveoli (hyaline membranes) – causes significant decrease in lung compliance (death in 70%)
  4. Regeneration of Type 2 alveolar lining cells & inflammation of interstitium
  5. Organisation leading to interstitial fibrosis
  6. Mild focal fibrosis: recovery with minimal respiratory dysfunction (10%) OR marked interstitial fibrosis (honeycomb lung) leading to death due to chronic severe respiratory impairment (20%)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the two phases of ARDS?

A
  1. Acute Exudative Phase
    - interstitial edema and high protein exudation into alveoli
    (fibrin-rich fluid +. necrotic epithelial cells)
  2. Late reorganisation phase
    - regeneration of type 2 alveolar lining cells, organisation of hyaline membranes with fibrosis
    - interstitium widened by mixture of inflammatory cells & scar tissue
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How do COVID-19 patients die?

A

“cytokine storm” in response to the virus in the lung causes ARDS = stiff lungs

mechanical ventilation & 100% oxygen may not be sufficient to treat respiratory failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the reslt of end stage of chronic pulmonary fibrosis?

A

Honeycomb Lung - small alveoli replaced by large cystic spaces

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the consequence of end stage pulmonary fibrosis?

A

Chronic Respiratory Impairment and reduced diffusion capacity

Death due to combination of respiratory and cardiac failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What histological pattern can be seen in acute damage to lungs? What modality is this seen on? What other imaging modality is used for diagnosis?

A

‘DAD’ diffuse alveolar damage in ARDS. Microscopy of lung biopsy. High resolution CT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is idiopathic pulmonary fibrosis?

A

Commonest chronic diffuse parenchymal lung disease

no cause

Progressive restrictive lung disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How does idiopathic pulmonary fibrosis present on microscope.

A

Usual interstitial pneumonia pattern

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is hypersensitivity pneumonitis/extrinsic allergic alveolitis?

A

Lung disease due to hypersensitivity to inhaled organic antigens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the cause of hypersensitivity pneumonitis/extrinsic allergic alveolits?

A
  1. Aninal Proteins
  2. Microbial Agents in vegetable matter 9fungi in mouldy crops, hay, compost)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

When might symptoms of hypersensitivity pneumonitis/extrinsic allergic alveolits occur?

A

Acute (4-8h)
Chronic (insidious development of dyspnea and pulmonary fibrosis in patient with no acute symptoms)8

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is pneumoconiosis?

A

Disease of lungs caused by inhalation of dust
- silica
- coal dust
-asbestos

interaction of dust with defence mechanisms of lung, leading to inflammation, release of cytokines and stimulation of fibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What usually is a risk factor for pneumoconiosis?

A

Occupational Exposure

17
Q

What factors worsen pneumoconiosis?

A
  1. Size of particles
  2. Smoking
18
Q

What are 5 lung diseases associated with asbestos?

A
  1. Pleural Plaques
  2. Pleural Effusions and thickening
  3. Progressive chronic lung fibrosis (asbestosis)
  4. Malignant mesothelioma
  5. Lung carcinoma
19
Q

What are granulomas?

A

Histological manifestations of cell mediated immunity

20
Q

What are 3 causes of granulomas in the lung?

A
  1. Infection *TB, fungal infection
  2. Foreign material.antigens (pneumoconiosis, hypersensitivity pneumonitis)
  3. Unknown (sarcoidosis)
21
Q

Where else apart from the lung might granulomas be seen?

A

Lymph node - immune reaction takes place in the draining lymph nodes too

22
Q

What is sarcoidosis?

A

systemic disease of unknown cause characterised by non-necrotising granulomas in many tissues and organs

involves intra-thoracic lymph nodes and/or lung 90%

23
Q

What are common sites of involvement apart from lymph node and lung?

A

Spleen, liver, bone marrow, skin, eye, lacrimal gland, salivary gland

24
Q

Amongst which population group is it common and amongst which is it rare?

A

CommoN: Caucasians, Blacks, Indians
Rare: Chinese, South East Asians