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
What is the mechanism of allergic asthma?
IgE-mediated type 1 hypersensitivity reaction (Th2 response)
26
This pulmonary congenital anomaly presents in the first two years of life with respiratory distress and cyanosis.
Congenital cystic adenomatoid malformation
27
What histologic findings are present in an asthmatic airway?
Goblet cell hyperplasia, fibrosis of the basement membrane, eosinophilic inflammation, smooth muscle hyperplasia
28
What is pulmonary sequestration?
A congenital anomaly in which a discrete area of lung tissue is not connected to the airways. May be intralobar or extralobar