week 1 restrictive Flashcards

(44 cards)

1
Q

What is bronchial asthma?

A

A heterogeneous group of diseases characterized by chronic airway inflammation, variable expiratory airflow obstruction, and symptoms such as wheezing, dyspnea, chest tightness, and cough that vary over time and in intensity.

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2
Q

What are the two main types of asthma based on prior sensitization to allergens?

A

Atopic (Extrinsic) Asthma

Non-atopic (Intrinsic) Asthma

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3
Q

What is the immunological mechanism in atopic asthma?

A

Type I (IgE-mediated) hypersensitivity reaction.

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4
Q

What are the common environmental triggers in atopic asthma?

A

Dust, pollen, animal dander, and certain foods.

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5
Q

What are the key features of atopic asthma?

A

Childhood onset

Positive family history

Positive skin test (wheal and flare)

Increased serum IgE

Associated with atopic diseases (e.g., allergic rhinitis, eczema)

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6
Q

What are the key features of non-atopic asthma?

A

Triggered by viral infections or irritants (e.g., SO₂, NO₂, O₃)

Normal serum IgE

Negative skin test

No associated atopy

No age preference

Less family history involvement

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7
Q

What is the pathogenesis of airway remodeling in atopic asthma?

A

Chronic inflammation leads to structural changes in the bronchial wall, known as airway remodeling.

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8
Q

List features of airway remodeling in asthma.

A

Thickened airway wall

Sub-basement membrane fibrosis

Increased vascularity

Increased submucosal gland size and number

Goblet cell hyperplasia

Smooth muscle hypertrophy/hyperplasia

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9
Q

What is the pathogenesis of drug-induced (aspirin-sensitive) asthma?

A

COX inhibition → Increased leukotriene synthesis → Bronchoconstriction. Common in patients with nasal polyps and rhinitis.

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10
Q

What triggers occupational asthma?

A

Fumes (epoxy), organic dusts (wood, cotton), gases (toluene), and chemical exposures after repeated contact.

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11
Q

What are the gross pathological features in fatal asthma?

A

Hyperinflated lungs

Airways occluded by thick mucus plugs

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12
Q

What microscopic findings are seen in asthma sputum/bronchoalveolar lavage?

A

Curschmann spirals – Whorls of shed epithelium in mucus

Charcot-Leyden crystals – Eosinophil protein crystalloids

Eosinophils

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13
Q

What are the clinical features of an asthma attack?

A

Dyspnea, expiratory wheezing, chest tightness, and cough (with or without sputum), worse at night or early morning.

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14
Q

What is status asthmaticus?

A

A severe, prolonged asthma attack that does not respond to standard therapy and can lead to respiratory failure.

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15
Q

What spirometry findings are seen during an asthma attack?

A

FEV1 < 30%

Decreased FEV1:FVC ratio

May be normal between attacks with residual deficits

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16
Q

What lab findings may support asthma diagnosis?

A

Eosinophilia in CBC

ABG: Hypoxemia, hypercapnia, respiratory acidosis

Sputum: Curschmann spirals, Charcot-Leyden crystals

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17
Q

What are the treatment options for asthma?

A

Avoid triggers

Bronchodilators

Leukotriene blockers

Long-term: Inhaled corticosteroids

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18
Q

How is parenchymal restrictive lung disease characterized?

A

Normal FEV1:FVC

Reduced DLCO

Increased A-a gradient

19
Q

How is extra-parenchymal restrictive lung disease characterized?

A

Normal FEV1:FVC

Normal DLCO

Normal A-a gradient

20
Q

What are the two main categories of restrictive lung disease?

A

Parenchymal and Extra-parenchymal.

21
Q

What characterizes parenchymal restrictive lung diseases on spirometry and gas exchange?

A

Normal FEV1:FVC, reduced DLCO, increased A-a gradient.

22
Q

What characterizes extra-parenchymal restrictive lung diseases?

A

Normal FEV1:FVC, normal DLCO, and normal A-a gradient.

23
Q

Give examples of extra-parenchymal causes of restrictive lung disease.

A

Chest wall disorders, kyphoscoliosis, neuromuscular diseases (e.g., myasthenia gravis), obesity, pleural disorders (effusions/pneumothorax).

24
Q

What structures make up the lung interstitium?

A

Basement membranes, collagen, elastin, fibroblasts, and mononuclear inflammatory cells.

25
What is the hallmark feature of ILD?
Involvement of the lung interstitium.
26
What are common clinical features of ILD?
Dyspnea on exertion, dry cough, hypoxia, pulmonary hypertension, cor pulmonale.
27
What is the underlying pathological process in ILD?
Alveolar damage → cytokine release → interstitial fibrosis → decreased lung compliance.
28
What does spirometry and gas exchange typically show in ILD?
Normal or increased FEV1:FVC, reduced DLCO, increased A-a gradient.
29
What is the imaging modality of choice for ILD?
High-Resolution CT (HRCT).
30
Name 3 fibrosing types of ILD.
Idiopathic pulmonary fibrosis, nonspecific interstitial pneumonia, pneumoconiosis.
31
Name 2 granulomatous ILDs.
Sarcoidosis, hypersensitivity pneumonitis.
32
Name 2 smoking-related ILDs.
Desquamative interstitial pneumonia, respiratory bronchiolitis-associated ILD.
33
Name 2 "other" types of ILD.
Langerhans cell histiocytosis, pulmonary alveolar proteinosis.
34
What is IPF?
A progressive, fibrosing interstitial lung disease causing respiratory failure.
35
What is the histologic term for IPF?
Usual interstitial pneumonia (UIP).
36
Who is most commonly affected by IPF?
Older males (55–75 years); rare before age 50.
37
What are possible environmental triggers for IPF?
Smoking, occupational exposures.
38
Describe the gross pathology of IPF.
Cobblestone pleural surface, subpleural and lower lobe fibrosis, honeycomb cysts.
39
Describe the histologic features of IPF.
Patchy fibrosis, temporal and spatial heterogeneity, fibroblast foci, honeycomb changes.
40
What are hallmark histologic signs of UIP?
Fibroblast foci, myxoid matrix, subpleural accentuation, honeycomb cysts.
41
What are the clinical symptoms of IPF?
Insidious dry cough, exertional dyspnea, cyanosis, clubbing, cor pulmonale in late stages.
42
What is the prognosis of IPF?
Poor; median survival ~3–5 years, 5-year survival ~20%.
43
What is the only definitive treatment for IPF?
Lung transplantation.
44
What must be ruled out before diagnosing IPF?
Other causes of UIP pattern (e.g., asbestosis, autoimmune disease).