Embryology Flashcards

1
Q

Where is the respiratory diverticulum/lung bud found?

A

The ventral wall of the foregut

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2
Q

Which germ layer is the foregut a part of?

A

Endoderm

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3
Q

On what day do the lung buds appear?

A

22

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4
Q

What separates the respiratory diverticulum from the foregut?

A

Tracheoesophageal ridges

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5
Q

What is a tracheoesophageal fistula (TOF)?

A

Incomplete division of foregut into oesophageal and respiratory portions.

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6
Q

What is the most common (85-90%) TOF?

A

oesophageal atresia

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7
Q

What is the second most common TOF?

A

connection of oesophagus to trachea

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8
Q

What are the symptoms of tracheoesophageal fistula with oesophageal atresia?

A

Abdomen rapidly distends as fills with air
Regurgitation of milk
Coughing
Stomach acid and bile in trachea- infection

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9
Q

What are the symptoms of a connection between the oesophagus and trachea?

A

Milk in respiratory system

No regurgitation as can still swallow milk

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10
Q

Which other congenital abnormalities are TOFs usually associated with?

A

VACTERL:

Vertebral defects (spina bifida)
Anal atresia
Cardiac defects -1/3 OF CASES
Tracheoesophageal fistulas 
Oesophageal atresia
Renal abnormailities
Limb defects  (common)
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11
Q

During what week are the lobar bronchi formed?

A

5

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12
Q

During what week are tertiary bronchi formed?

A

6

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13
Q

How many lobar bronchi are in each lung?

A

3 on right, 2 on left

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14
Q

How many tertiary bronchi are in each lung?

A

10 on right, 8 on left

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15
Q

When are terminal bronchioles formed?

A

Week 16

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16
Q

When are respiratory bronchioles formed?

17
Q

When do the first alveoli develop?

18
Q

How is branching partially regulated?

A

Interaction of the epithelium (from foregut) with the overlying visceral mesoderm (which will form cartilage, smooth muscle, connective tissue and capillaries)

19
Q

From where are the capillaries, smooth muscle, cartilage and connective tissue derived?

A

The visceral mesoderm.

20
Q

What are the visceral and parietal pleura derived from?

A

Visceral and parietal mesoderm.

21
Q

What is pulmonary agenesis?

A

When the lung bud fails to split resulting in the complete absence of bronchi and vasculature. Unilateral or bilateral. Bilateral is incompatible with life.

22
Q

What is pulmonary hypoplasia?

A

All components present but incompletely developed. Severity varies. May be in association with congenital diaphragmatic hernia.

23
Q

What is branching morphogenesis?

A

Extra lobes or segments- little functional significance.

24
Q

What are the four periods of lung maturation?

A
  1. Pseudoglandular
  2. Canalicular
  3. Terminal Sac
  4. Alveolar
25
When is the pseudoglandular period?
5-17 weeks
26
What happens during the pseudoglandular period?
The respiratory tree branches to form terminal bronchioles. Respiration not possible
27
When is the canalicular period?
16-25 weeks
28
What happens during the canalicular period?
Terminal bronchioles give rise to respiratory bronchioles which give rise to alveolar ducts. Mesodermal tissue becomes highly vascularised. Respiration possible towards the end.
29
When is the terminal sac period?
26 weeks - birth
30
What happens during the terminal sac period?
Further terminal sacs develop Epithelium thins and capillaries come into 'contact' with it Blood-air barrier formed Type I and type II pneumocytes formed from differentiation of epithelium Surfactant produced, facilitating inflation. Survival possible but may have respiratory distress syndrome
31
When is the alveolar period?
36 weeks-8 years
32
What happens during the alveolar period?
Increase in number of respiratory bronchioles and alveoli (95% mature alveoli don't develop until after birth)
33
When do breathing movements start?
In utero, to remove amniotic fluid and to practice muscles of respiration
34
What happens to lung fluid after birth?
It is reabsorbed into the capillaries
35
How is infant respiratory distress syndrome treated?
- Glucocorticoid treatment accelerates foetal lung development and surfactant production - Surfactant therapy- natural or artificial
36
What genetic condition can also affect surfactant?
Surfactant protein B deficiency disease Fatal even with replacement therapy. This protein only makes up 2% of surfactant but is very important. Autosomal recessive.