Embryology of the reparatory system Flashcards

1
Q

what is the point of transition between the upper and respiratory tract

A

the larynx

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2
Q

what are the structures of the upper respiratory tract

A

nasal cavities
nasopharynx
oropharynx
(larynx)

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3
Q

what are the structures of the lower respiratory pathway

A
(larynx) 
trachea 
bronchi 
bronchioles 
terminal bronchioles 
respiratory bronchioles 
alveolar ducts 
a sacs 
alveoli
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4
Q

where does the respiratory portion start

A

reparatory bronchioles - alveoli

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5
Q

which germ layer produces the inner epithelia and the connective structures of the lungs

A

inner epithelia - endoderm

connective structure - mesoderm

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6
Q

which part of the gut tube does the respiratory diverticulum develop from

A

foregut in week 4

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7
Q

which day does the respiratory diverticulum appear

A

lung buds develop day 22

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8
Q

what direction do the lung buds grow

A

ventrocaudally

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9
Q

what separates the reparatory diverticulum from the oesophagus (foregut)

A

tracheosophageal ridges (except laryngeal inlet)

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10
Q

what is the orientation of the oesophagus and the trachea

A

trachea is anterior to the oesophagus

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11
Q

what is a fistula

A

an abnormal communication

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12
Q

what are the two types of malformations in development of the lungs

A

atresia with fistula 85-90%

fistula

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13
Q

why do malformations occur

A

incomplete division of foregut into oesophageal and respiratory proteins

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14
Q

what is an atresia

A

proximal closing off of the oesophagus

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15
Q

what is tracheoesophageal fistula with oesophageal atresia and what are the problems associated with it

A

upper oesophagus ends abruptly, lower oesophagus forms fistula with trachea - causes abdomen rapidly to distend as stomach fills with air
the atresia causes air sacs to be filled with milk and other contents from the stomach such as enzymes and acid

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16
Q

what is H type tracheoesphaogeal fistula

A

communication between oesophagus and trachea
approx 4% of cases
milk goes into respiratory system and causes infection

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17
Q

TOF are usually associated with other congenital abnormalities what are they

A
V - vertebral defects 
A - anal atresia 
(C) - cardiac defects 
T - tracheooseophageal fistulas 
E - Esophageal atresia 
R - Renal abnormalities 
(L) - limb defects
18
Q

what happens in week 5 to the lungs

A

further growth and differentiation - formation of main bronchi and secondary bronchi (day 30)
3 on the right and 2 on the left

19
Q

what happens to development during the 6th week

A

tertiary bronchi - which each supply a bronchopulmonary segment
10 right and 8 left

20
Q

branching stages are different during development
what occurs at week 16
26
36

A

terminal bronchioles - 16
respiratori bronchioles - 26 (poor gas exchange can occur)
alveoli - 36

21
Q

what forms from the visceral mesoderm

A

cartilage, smooth muscle, connective tissue capillaries and visceral mesoderm

22
Q

what are the two formations of the pleura

A

visceral mesoderm - visceral pleura
parietal mesoderm - parietal pleura
lateral plate of the mesoderm forms the pleura

23
Q

what is pulmonary agenesis

A

failure for lung to form properly

occurs when lung bud fails to split causing complete absence of bronchi and vasculature

24
Q

what is the clinical presentation of pulmonary agenesis

A

child usually develops respiratory distress
remaining lung is compromised - usually lower respiratory tract infection
common with vertebra for rib anomalies

25
what can happen to the lung in unilateral pulmonary agenesis
enlarge
26
what is pulmonary hypoplasia
incomplete development of the lungs severity determines extent of development may be found in association with congenital diaphragmatic hernia
27
what is branching morphogenesis
produce azygous lobe (extra lobe) - little functional difference
28
what are the four periods of maturation of the lungs
``` (embryonic) pseudoglandular canalicular saccular/terminal sac alveolar there is overlap between the stages ```
29
what week does surfactant start to get produced
around the 25/26th week
30
what is the difference in weeks of the embryonic and the fetal period
embryonic - 2-8 weeks | fetal - 8-38 weeks
31
what happens during the pseudoglandular period and what is the rough time span of the period
5-17 weeks branching of the respiratory tree has occurred to form terminal bronchioles (respiration still cannot occur - still part of the conduction pathway)
32
what happens during the canalicular period and what is the rough time span
16-25 weeks terminal bronchioles give rise to respiratory bronchioles which give rise to alveolar ducts mesodermal tissue becomes highly vascularised respiration possible towards the end of this period towards the end of this period there is better prognosis for birth but low chance of fetal survival
33
what is the rough time span of the terminal sac/ saccular period and what occurs
from week 26 until birth primitive alveoli are developed epithelium thins and capillaries come into contact with epi blood air barrier formed surfactant forms a film over the internal walls - facilitating inflammation of the lungs
34
what does the epithelium differentiate into and in what period
saccular period - divides into type 1 neumocytes where gas exchange occurs types 2 pneumocytes where surfactant is produced
35
what is most likely to happen to a fetus born prematurely at 24 week s
respiratory distress syndrome
36
what is the alveolar period
36 - 8 years development of he lugs which increase in number of alveoli and respiratory bronchioles 95% of mature alveoli do not develop until after birth
37
what happens to the lungs during birth
breathing starts in utero to remove amniotic fluid - kick starts respiration in muscles remaining lung fluid is rapidly absorbed into capillaries
38
what is the prime factor in prognosis if child is born prematurely
development of the lungs
39
what is respiratory distress syndrome
eg birth at 23 weeks laboured breathing increased rate of breathing mechanical ventilation needed damage to alveolar lining as fluid and serum leak into alveoli can lead to bronchopulmonary dysplasia (abnormal formation)
40
what are the treatments for respiratory distress syndrome
glucocorticoid treatment accelerates fetal lung development and surfactant production surfactant therapy - natural/artificial replacement - use surfactant A and B proteins)
41
what is surfactant protein B deficiency
autosomal recessive loss of surf pros B which is fatal and need replacement therapy