Lung development Flashcards

1
Q

What is the embryonic stage?

A

3-8 weeks

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2
Q

What is the pseudo glandular stage

A

5-17 weeks

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3
Q

what is the canalicular stage?

A

16-26 weeks

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4
Q

what is the saccular stage?

A

24-38 weeks

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5
Q

what is the alveolar stage?

A

36 weeks- 2/3 years

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6
Q

Pulmonary hypertension in chronic respiratory disease occurs due to chronic hypoxia.

Select one:

True

False

A

True – hypoxia triggers a reflex constriction of pulmonary vessels, and this constriction increases the vascular resistance and therefore the pressure of the pulmonary circulation.

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7
Q

what phase does lung bug develop first as a bud and where from?

A

in the embryonic phase via fetal foregut

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8
Q

The embryonic lung buds are derived from the foregut.

Select one:

True

False

A

True – the lungs begin as an outpouching of the foregut, hence the close proximity of the trachea to the oesophagus.

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9
Q

at how many weeks are there 2 primary lung buds visible?

what does this make?

A

5 weeks

this makes the lobar buds = 3 on right 2 on left

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10
Q

the cells of the lung are derived from

A

like cells of the gut, lung cells are derived from endotherm

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11
Q

blood vessels and tissues are derived from what type of cell?

A

blood vessels connective tissues surrounded by mesoderm

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12
Q

what embryonic phase for lung development is at 5-17 weeks?

A

pseudoglandular phase - lung morphogenesis

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13
Q

how many weeks is the pseudo glandular phase in embryology for lung development

A

5-17 weeks

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14
Q

what happens to the lungs at the pseudo glandular stage of embryonic lung development?

A

rapid branching of the airway

16-25 primitive segmental bronchi which continue to elongate

specialising cilia and mucus glands appear airways

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15
Q

Which phase involves the lung developing distal architecture

A

canalicular 16-26 weeks

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16
Q

canalicular stage what is formed

A

type 1 and type 2 pneumocytes form a very thin membrane

17
Q

in the later phase of canalicular what happens?

A

specialised cells mature which allows a baby to survive successfully if born prematurely with intensive care support

18
Q

how many weeks can an infant be to survive

A

24 weeks. especially with improves natal care.

even 22 and 24 weeks although high-risk morbidity and mortality.

19
Q

saccular stage 24-38 weeks

A

become alvioli after birth form well. more surfactant produces. bronchioles elongate interstitial tissue between sac reduced alveolar walls become thinner to improve gas exchange

20
Q

alveolar stage 26 weeks - term and 2 years

A

lungs independently sustain breathing without support cells well differentiated

pulmonary vasculature well developed forming final alveolar structures

21
Q

healthy foetus how many airsacs

A

20-50 million at birth and 200-30 million age 3-8

22
Q

common upper respiratory congenital abnormalities respiratory

A

Pierre-robin sequence; choanal stenosis/atresia

laryngomalacia and tracheomalacia; treacheo-oesophageal fistula

laryngeal atresia; tracheal atresia and stenosis; laryngeal web and cyst

*Atresia is a condition in which an orifice or passage in the body is (usually abnormally) closed or absent.*

23
Q

common lower respiratory congenital abnormalities respiratory

A

pulmonary hypoplasia

bronchogenic cyst

CPAM

congenital diaphragmatic hernia

bronchial atresia and stenosis

24
Q

how are gongenital respiratory abnormalities usually picked up?

antenatal

A

antenatal scanning

  • ultrasound

MRI (fetal)

25
symptoms of congenital respiratory abnormalities newborn
tachypnoea respiratory distress feeding issues
26
symptoms of congenital respiratory abnormalities child
stridor/wheeze recurrent pneumonia cough feeding issues
27
describe laryngomalacia
malacia (softening) - softening of the voice box commonly seen in infants presents with stridor, worse when feeding or when upset/excited will improve in the first year only concern if child struggles to feed, growth or colour change
28
tracheomalcia
malacia (softening) of the trachea can be isolated in healthy infants associated with genetic conditions maybe caused by external compression (e.g. vessels/tumour) - bronchoscopy to find presentation: barking cough, recurrent croup, breathless on exertion, stridor/wheeze usually resolved on own, may need physio and antibiotics if unwell.
29
tracheo-oesophageal fistula
- abnormal connection between trachea and oesophagus the majority have associated with oesophageal atresia (closing) association genetic conditions presentation: normally diagnosed antenatally or postnatally: choking colour change cough when feeding unable to pass ng tube treatment: surgical repair complications: tracheomalacia, strictures, leak and reflux
30
congenital pulmonary airway malformation (CPAM)
- abnormal non-functioning lung tissue; - 80%detected antenatally; - occurs sporadically -many resolve spontaneously in utero - conservative if asymptomatic - surgical intervention may be required - possible risk of malignant change
31
congenital diaphragmatic hernia
the diaphragm forms from multiple tissues around 7 weeks and closes by 18 weeks CHD affects 1 in 2500 births different typed most common bochdalek 90% usually left side more common than the right side most diagnosed antenatally some cases late diagnoses (earlier the better) need to be transferred to ITU due to significant morbidity and mortality surgical repair prognosis depends on degree of lung hypoplasia
32
where can lung remodelling of the lung can occur (child development)
seen in asthma and chronic lung disease of prematurity Chronic inflammation - increased bronchial responsiveness increase mucus secretion airway oedema airway narrowing
33