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
Q

symptoms of congenital respiratory abnormalities newborn

A

tachypnoea

respiratory distress

feeding issues

26
Q

symptoms of congenital respiratory abnormalities child

A

stridor/wheeze

recurrent pneumonia

cough

feeding issues

27
Q

describe laryngomalacia

A

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
Q

tracheomalcia

A

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
Q

tracheo-oesophageal fistula

A
  • 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
Q

congenital pulmonary airway malformation (CPAM)

A
  • 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
Q

congenital diaphragmatic hernia

A

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
Q

where can lung remodelling of the lung can occur (child development)

A

seen in asthma and chronic lung disease of prematurity

Chronic inflammation - increased bronchial responsiveness

increase mucus secretion

airway oedema

airway narrowing

33
Q
A