Pathome - COPD Flashcards

1
Q

What are the 4 chronic obstructive pulmonary diseases?

A

Chronic bronchitis

Emphysema

Asthma

Bronchiectasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the classic lung volume finding in COPD

A

FEV1/FVC < 80%

Both are decreased, but FEV1 is decreased more

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Describe the basic premise behind COPD

A

Due to obstruction of airflow

Air trapping in the lungs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the diagnostic definition of chronic bronchitis

A

Chronic productive cough lasting at least 3 months over a minimum of 2 consecutive years

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe the pathophysiology behind chronic bronchitis

A

Hypertrophy of bronchial mucinous glands

Reid index (thickness of mucosal gland layer relative to bronchial wall thickness) >50%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Does chronic bronchitis cause “pink puffers” or “blue bloaters” and why?

A

Blue bloater

Mucus plugs trap CO2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How can COPD lead to cor pulmonale?

A

When there is lack of O2 to majority of the lung, all those blood vessel will constrict, leading to pressure backing up to R heart, leading to R heart failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Describe the pathophysiology behind emphysema

A

Destruction of alveolar air sacs due to (1) loss of elastic recoil and (2) collapse of airways

Leads to physiologic obstruction and air trapping

Think of a large grocery bacg instead of multiple small balloons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the cause of destruction of alveolar air sacs in emphysema

A

Imbalance of proteases (destroy pathogens that make it to small airways e.g. elastase) and anti-proteases

(1) Inflammation = increased proteases (e.g. smoking)
(2) Decreased anti-proteases = a1-anti-trypsin deficiency (A1AT is what neutralizes elastase)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What type of emphysema will you see in smoking vs. A1AT deficiency

A

Smoking: centri-acinar emphysema more in upper lobes

A1ATD: pan-acinar emphysema more in lower lobes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q
A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What other organ does A1ATD affect and why?

A

Liver cirrhosis

Liver is still making A1AT, but mutation causes it to be misfolded, so protein accumulates in hepatocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What part of the hepatocyte does misfolded A1AT accumulate in and what does biopsy reveal

A

Endoplasmic reticulum

Biopsy shows PAS-positive globules in hepatocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the normal/abnormal alleles in A1ATD

A

PiM is normal; PiZ is abnormal

PiMZ heterozygotes are usually asymptomatic but have significant risk of emphysema with smoking

PiZZ homozygotes are at significant risk for panacinar emphysema and cirrhosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Does emphysema cause “blue bloaters” or “pink puffers” and why?

A

Pink puffers

Patients are able to prevent airway collapse by pursing lips and exhaling slowly in order to create back-pressure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is a common gross/x-ray appearance in emphysema

A

Barrel-shaped chest

17
Q

Describe the basic premise of asthma

A

Reversible airway bronchoconstriction, usually due to allergic stimuli

18
Q

Describe the pathogenesis of type I hypersensitivity in asthma

A

Allergens induce Th2 cells

Th2 cells secrete IL-4 (IgE class switching), IL-5 (eosinophils), and IL-10 (increased Th2 and inhibiton of Th1)

Reexposure to allergen leads to IgE-mediated activation of mast cells

Mast cells release:

(1) Histamine (vasodilaiton and increased permeability)
(2) Leukotrienes (bronchoconstriction)

19
Q

Describe 2 histologic findings in asthma

A

(1) Curschmann spirals (shed epithelium forms wholed mucus plug)
(2) Charcot-Leyden crystal (eosinophil-dervied needle-like crystals) - see next slide for image

20
Q

Charcot-Leyden crystals

A

eosinophil-dervied needle-like crystals

21
Q

Describe the basic premise of bronchiectasis

A

Permanent dilation of bronchioles and bronchi

Dilation leads to turbulent airflow instead of accelerated, straight line flow –> air trapping

22
Q

What are the causes of bronchiectasis

A

Necrotizing inflammation with damage to airway walls:

  • Cystic fibrosis
  • Kartagener sydrome
  • Tumor or foreign body
  • Necrotizing infection
  • Allergic bronchopulmonary aspergillosis
23
Q

What is Kartagener syndrome?

A

Defect in the dynein arm of cilia

Leads to sinusitis, infertility, situs inversus, bronchiectasis