Pathology of Obstructive Airway Disease Flashcards

1
Q

These are extrusions of mucus plugs commonly found in cases of asthma exacerbation.

A

Curschmann spirals

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2
Q

Cor pulmonale is most associated with what type of COPD?

A

Chronic bronchitis

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3
Q

This disorder is autosomal recessive and caused by mutations resulting in ciliary dysfunction the prevents mucus clearance.

A

Primary ciliary dyskinesia

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4
Q

What is bronchiectasis?

A

Permanent dilation of the airways due to excess mucus

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5
Q

Acute lung injury is caused by abrupt onset hypoxemia and bilateral pulmonary edema. What is the cause of edema?

A

Increased vascular permeability due to inflammation

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6
Q

What trisomies are associated with pulmonary hypoplasia?

A

Trisomies 13, 18, & 21

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7
Q

What symptoms characterize Samter’s triad?

A

Asthma, sinus disease with nasal polyps, NSAID sensitivity (esp. aspirin)

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8
Q

What occurs during the proliferative phase of ARDS?

A

Proliferation of Type 2 pneumocytes and alveolar thickening by fibroblasts

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9
Q

What are the different mechanisms of atelectasis?

A

Resorption, compression, contraction (fibrosis)

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10
Q

True/False. Bronchogenic cysts present early in life with acute respiratory distress and cyanosis.

A

False - bronchogenic cysts present later in life and are often asymptomatic.

Congenital cystic adenomatoid malformation present early in life with acute respiratory distress and cyanosis.

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11
Q

What is atelectasis?

A

Incomplete expansion or collapse of a lung

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12
Q

This is a specific type of atelectasis caused by compression from the hilar lymph nodes.

A

Right middle lobe syndrome - obstruction of the right bronchus to the right middle lobe

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13
Q

What acid/base imbalance is associated with ARDS?

A

Respiratory acidosis

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14
Q

This is a nonspecific histologic finding common in patients with chronic lung disease.

A

Creola bodies - groups of reactive bronchial cells

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15
Q

What is the cause of neonatal respiratory distress syndrome?

A

Deficiency in pulmonary surfactant produced by type 2 pneumocytes

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16
Q

What are Charcot-Leyden crystals?

A

Crystals of eosinophils found in asthmatics

17
Q

This pulmonary congenital anomaly is characterized by incomplete of defective lung development.

A

Pulmonary hypoplasia

18
Q

This type of emphysema is associated with spontaneous pneumothorax in young adults.

A

Paraseptal/Localized emphysema - bullae lesions adjacent the pleura

19
Q

What is the most common type of emphysema?

A

Centriacinar - lesions in the upper lobes associated with cancer

20
Q

This type of emphysema presents with lesions in the lower zones and is associated with a1-antitrypsin deficiency.

A

Panacinar emphysema

21
Q

What are the stages of acute respiratory distress syndrome?

A

Acute exudative phase, proliferative phase, late fibrotic stage

22
Q

Hyaline membranes form during what phase of ARDS?

A

Acute exudative phase - within one week of injury

23
Q

This pulmonary congenital anomaly is characterized by focal obliteration of the proximal segment of a bronchus.

A

Bronchial atresia

24
Q

This is a classic histologic finding in acute respiratory distress syndrome.

A

Hyaline membranes

25
Q

What is the mechanism of allergic asthma?

A

IgE-mediated type 1 hypersensitivity reaction (Th2 response)

26
Q

This pulmonary congenital anomaly presents in the first two years of life with respiratory distress and cyanosis.

A

Congenital cystic adenomatoid malformation

27
Q

What histologic findings are present in an asthmatic airway?

A

Goblet cell hyperplasia, fibrosis of the basement membrane, eosinophilic inflammation, smooth muscle hyperplasia

28
Q

What is pulmonary sequestration?

A

A congenital anomaly in which a discrete area of lung tissue is not connected to the airways. May be intralobar or extralobar