developmental aspects of lung disease Flashcards

1
Q

what arw the stages of lung morphogenesis

A
embryonic 3-8 weeks 
paeudoglandular 5-17
canalicukar 16-26
saccukar 24-38
alveolar 36 to 2/3 years
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2
Q

what happens in the embryonic phase

A

lung bud starts to develop from foetal foregut
at 5 weeks two primary lung buds are visible which later become lobar buds of which 3 on right and 2 on left
derived from endoderm

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3
Q

what happens in the pseudoglandular ohase

A

rapid branching of airways
eventually 16-25 prinaribe segmentive bronchi
cilia and mucous glands start to apprar

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4
Q

what is the canalicukar phase

A

phase where lungs develop dostal architecture
terminal bronchioles, alveolar sace and capillary blood vessels form gas exhange units
thoe 1 and 2 pneumocytes form

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5
Q

what happens in the saccular phase

A

albeolar sacs grow and become well formed
more surfactant productedb
interstitial tissue between sacs decrease
alveokar sace thin

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6
Q

what happens in the alveolar stage

A

independently sustain breathing withour support

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7
Q

what are common congenital abnormalities

A

UPPER
laryngomalacia and tracheomalacia
tracheo - oesophageal fistula

LOWER
COAM
congenital diaphragmatic hernia

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8
Q

how do you find congenital abnormalities

A

antenatal scanning

  • ultrasound
  • MRI

newborn

  • tachypnoea
  • resp distress
  • feeding issues

childhood

  • stridor/ cough
  • recurrent oneumonia
  • wheeze
  • feeing issues
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9
Q

what is laryngomalacia

A

softening of the larynx
commonly seen in infants
present w strodor worse w feeing or when upset/excited
will imrove within first year
concern if it effects deeding, growth or causes wonorad

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10
Q

what is tracheomalacia

A
floppiness of trachea 
associated w genetic conditions 
or external compression 
presbtw w a barking cough
recurrent croup
breathlessness on exertion 
stridor or wheeze
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11
Q

who do u manage tracheomalacia

A

physio and antibiotics

batural history resolution w time

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12
Q

what is tracheo - oespphageal fistula

A

abnormal connectuon between trachea and oesophagus
majorify have associated oesophageal atresja
associagion w genetic conditions

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13
Q

how does a tracho oesophageal fistula oresent

A

choking
colour change
cough w feeding
unable to pass NG

treatment w surgical repair

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14
Q

what are complications w tracheo oesophageal fistula

A

tracheomalacia
strictures
leak
reflux

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15
Q

what is congenitak pulmonary airway malformation CPAM

A
abnormal non functioning lung tissue 
occur spontaneously 
may resokve spontaneoyslt in utero 
conservative management if asymptomatic 
may require surgical intervention
possible risk of malognant change
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16
Q

what is a congenitak diaphragmatic hernia

A

diaphrahm sometimes doesnt close at 18 weeks or not properly
usually the left side
management is surficak repair

17
Q

what is transient tachypnoea

A

fluid in lungs does not move as effectively due to lings inflating from child passing theough birth canal and first breatb
improves in 1-2 days

18
Q

what is resp dostressbsyndrome

A

surfactant deficiency
treated w antenatel sterouds
surfactant replacement
appropriate cent and butritoon

19
Q

what is remodelling

A
aleteration of airway structure 
environmwntal exposure (smoking)
chrinic diseases id childhood ( asthma) 
infectjon 
leads to abnormalities due to interference of inter cellukar signallinf
20
Q

what does chrinic i flammation keas ro

A

increased bronchial responsiveness
incrrase mucus secretion
airway oedema
airway narrowing