• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/13

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

13 Cards in this Set

  • Front
  • Back
  • 3rd side (hint)
Describe the major symptoms/signs of restrictive lung disease
1. Dyspnoea
2. Tachypnoea
3. End-inspiratory crackles
4. Eventual cyanosis
5. No wheezing (or other evidence of airways obstruction)
What are the 3 characteristic physiological features of restrictive lung disease?
Reduced ...
1. ... carbon monoxide diffusing capacity
2. ... lung volume
3. ... compliance
What might you expect to find on a CXR in infiltrative lung disease?
Bilateral infiltrative lesions, in the form of
1. ... small nodules
2. ... irregular lines
3. ... ground-glass shadows
Broadly, what are the 3 stages of interstitial lung disease?
1. Initial injury
2. Inflammation/fibrosis of pulmonary CT
3. Scarring and gross destruction of the lung (honeycomb lung)
What are the 5 categories Robbins divides interstitial lung disease into?
1. Fibrosing
2. Granulomatous
3. Eosinophilic
4. Smoking related
5. Other (pulmonary alveolar proteinosis)
What are 6 types of fibrosing interstitial lung disease (ILD)?
Two of unknown etiology:
1. Idiopathic pulmonary fibrosis (IPF)
2. Nonspecific interstitial pneumonia

Two associated with other illness:
3. Cryptogenic organizing pneumonia
4. ILD associated with connective tissue diseases

Two associated with known insults to the lung:
5. Pneumoconiosis
6. Complications of therapy
What is the name for the pathologic pattern of patchy interstitial fibrosis around edges, progressing to honeycomb lung?
This is usual interstitial pneumonia, or UIP.

It is seen in several of these conditions, but is the hallmark of idiopathic pulmonary fibrosis.
What are the important clinical differences between idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia?
Nonspecific interstitial pneumonia often occurs in younger patients, and is associated with a better prognosis.
Loose fibrous tissue plugs, with normal underlying lung, is characteristic of which disorder?
Cryptogenic organising pneumonia, AKA BOOP.
Hyalinised whorls of collagen, without notable inflammation, are characteristic of which disorder?
Silicosis.

Name some occupational risk factors for silicosis.
It is the most prevalent chronic occupational disease in the world. Mining/quarrying (gold, tin, copper, coal), sandblasting, metal grinding, and ceramics manufacture.
What are the symptoms of anthracosis, and simple and complicated coal worker's pneumoconiosis?
Anthracosis: asymptomatic.
Simple CWP: cough & blackish sputum
Complicated CWP: disabling respiratory insufficiency

What are the histological changes?
Anthracosis: accumulations of carbon
Simple CWP: above + coal macules (aggregates of coal-laden macrophages)
Complicated CWP: above + severe fibrosis and scarring
Case study:
You are sitting an exam. A question about sarcoidosis arises. What are 4 keywords you might mention?
Clinical:
1. Organomegaly
Pathology
2. Noncaseating granulomas
3. Schaumann bodies
4. Asteroid bodies
What are some examples of hypersensitivity pneumonitis?
Hypersensitivity pneumonitis conditions include farmer's lung, pigeon breeder's lung, humidifier/air conditioner lung, and many more.
These are hypersensitivity reactions, so they're marked by:
- bronchiolocentric interstitial pneumonitis and fibrosis
- noncaseating granulomas

Coal-workers pneumoconiosis is a fibrosing disease