Restrictive lung diseases Flashcards

(38 cards)

1
Q

What are two key characteristics of restrictive lung diseases?
A:

A
  1. The lungs are stiff and don’t expand well (inspiratory defect).
    1. The alveolar walls are damaged and replaced with scar tissue (fibrosis).
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2
Q

What happens to lung compliance in restrictive lung diseases?

A

A: Lung compliance decreases — the lungs become stiff

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3
Q

What does a chest X-ray show in restrictive lung diseases?

A

A: Bilateral diffuse pulmonary infiltrates.

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4
Q

What lung pattern may appear in late stages?

A

A: Honeycomb lung may appear.

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5
Q

What are the Clinical features of Cryptogenic Fibrosing Alveolitis ?

A

➔ Nonproductive cough & progressive dyspnea
➔ Cyanosis, clubbing, dry ‘crackles’ at inspiration
➔ Chest X ray → bilateral basal nodular infiltrates

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6
Q

What test helps confirm the diagnosis of Cryptogenic Fibrosing Alveolitis?

A

✅ Lung biopsy.

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7
Q

What are the morphology of Cryptogenic Fibrosing Alveolitis?

A

➔ Cobblestones (retraction of scars along the septa)

➔ ‘Temporal heterogeneity’

(Honeycomb Lung)

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8
Q

What type of inflammation is seen in Cryptogenic Fibrosing Alveolitis?

A

A: Interstitial chronic inflammation with fibroblastic proliferation.

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9
Q

Where in the lung does Cryptogenic Fibrosing Alveolitis mainly affect?

A

A: Peripheral areas, basal regions, along the pleura and septae.

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10
Q

How is the distribution of Nonspecific Interstitial Pneumonia?

A

A: It is more diffuse and without temporal heterogeneity.

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11
Q

What are the two main histologic patterns of Nonspecific Interstitial Pneumonia?

A

A: Mature fibrosing pattern and cellular pattern (infiltrate of lymphocytes and plasma cells).

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12
Q

What is the key histological feature of Cryptogenic Organizing Pneumonia?

A

A: Polypoid plugs of fibrosis in bronchioles, alveolar ducts, and alveoli.

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13
Q

What is the typical outcome of Cryptogenic Organizing Pneumonia with treatment?

A

A: Recovery within 6 months with steroid therapy.

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14
Q

What are examples of Collagen Vascular Diseases associated with interstitial lung disease?

A

A: Systemic Lupus Erythematosus (SLE), Rheumatoid Arthritis (RA), and Progressive Systemic Sclerosis (Scleroderma).

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15
Q

What is Anthracosis and who is commonly affected?

A

A: Anthracosis is the most common coal-related lung disease, often seen in tobacco smokers due to inhalation of carbon pigment

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16
Q

Does Anthracosis increase the risk of lung cancer?

A

A: No, it does not increase the risk of lung cancer.

17
Q

What are the types of Coal Workers’ Pneumoconiosis (CWP)?
A:

A

a. Simple CWP
b. Complicated CWP
c. Progressive Massive Fibrosis

18
Q

What characterizes Simple Coal Workers’ Pneumoconiosis (CWP)?

A

A: Presence of macules (dust-laden macrophages) and nodules (with collagen), mainly in upper lobes, with possible centrilobular emphysema.

19
Q

What is the most common occupational lung disease?مهم

A

A: Silicosis.

20
Q

What are common occupations at risk for Silicosis?

A

A: Sandblasting,

21
Q

What radiological sign is classic for Silicosis?

A

A: “Egg-shell” calcification in hilar lymph nodes on chest X-ray.

22
Q

What are the clinical features of Silicosis?
A:

A

• Often asymptomatic
• Dyspnea appears late
• Higher risk of tuberculosis
• Increased risk of lung cancer (especially with crystalline silica)

23
Q

What are Asbestos (Ferruginous) Bodies and where can they be found?
A:

A

• Found in sputum, bronchial wash, and lung tissue
• Composed of: asbestos fibers coated with protein and iron
• Show positive Perl’s stain (blue color for iron)
• May be seen even in normal individuals exposed to asbestos

24
Q

What cancers are associated with asbestos exposure?
A:

A

Malignant mesothelioma (pleural cancer)

25
What are the pleural complications of asbestos exposure?
• Pleural plaques: the most common lesion of asbestos exposure
26
Which populations are more commonly affected by Sarcoidosis?
A: It is more common in Black people in the US, Scandinavians, and nonsmokers.
27
What are the main organs affected by Sarcoidosis? A:
• Lungs and hilar lymph nodes • Skin, eyes, and lacrimal glands • Salivary glands • Liver, spleen, and bone marrow
28
What genetic markers are associated with a predisposition to Sarcoidosis?
A: HLA-A1 and HLA-B8 are genetic markers linked to increased risk of developing Sarcoidosis.
29
What are the characteristics of sarcoidosis?
➔ Non-caseating ➔ Bilateral hilar lymphadenopathy ➔ Hypercalcemia
30
What are the characteristics of sarcoidosis?
➔ Non-caseating ➔ Bilateral hilar lymphadenopathy ➔ Hypercalcemia
31
: What is the main chronic lung change in Hypersensitivity Pneumonitis?
A: Patchy interstitial inflammation with non-caseating granulomas and fibrosis.
32
What is Desquamative Interstitial Pneumonia (DIP)?
It is interstitial inflammation with many macrophages in alveolar spaces, often related to smoking.
33
How does Desquamative Interstitial Pneumonia (DIP) respond to treatment?
A: It usually responds well to steroids.
34
What blood test is helpful in diagnosing sarcoidosis?
A: ACE (Angiotensin Converting Enzyme) test — it is increased in sarcoidosis.
35
What is the confirmatory test for Usual Interstitial Pneumonia (UIP)?
A: Open lung wedge biopsy.
36
What are Masson bodies and where are they found?
A: Polypoid plugs of fibrosis seen in bronchioles, alveolar ducts, and alveoli; associated with Cryptogenic Organizing Pneumonia (BOOP).
37
What causes hemoptysis in bronchiectasis?
A: Injury or rupture of the bronchial artery.
38
Does emphysema cause cyanosis?
A: Not usually, unless combined with chronic bronchitis, as seen in centriacinar (centrilobular) emphysema.