developmental aspects of lung disease Flashcards
what arw the stages of lung morphogenesis
embryonic 3-8 weeks paeudoglandular 5-17 canalicukar 16-26 saccukar 24-38 alveolar 36 to 2/3 years
what happens in the embryonic phase
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
what happens in the pseudoglandular ohase
rapid branching of airways
eventually 16-25 prinaribe segmentive bronchi
cilia and mucous glands start to apprar
what is the canalicukar phase
phase where lungs develop dostal architecture
terminal bronchioles, alveolar sace and capillary blood vessels form gas exhange units
thoe 1 and 2 pneumocytes form
what happens in the saccular phase
albeolar sacs grow and become well formed
more surfactant productedb
interstitial tissue between sacs decrease
alveokar sace thin
what happens in the alveolar stage
independently sustain breathing withour support
what are common congenital abnormalities
UPPER
laryngomalacia and tracheomalacia
tracheo - oesophageal fistula
LOWER
COAM
congenital diaphragmatic hernia
how do you find congenital abnormalities
antenatal scanning
- ultrasound
- MRI
newborn
- tachypnoea
- resp distress
- feeding issues
childhood
- stridor/ cough
- recurrent oneumonia
- wheeze
- feeing issues
what is laryngomalacia
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
what is tracheomalacia
floppiness of trachea associated w genetic conditions or external compression presbtw w a barking cough recurrent croup breathlessness on exertion stridor or wheeze
who do u manage tracheomalacia
physio and antibiotics
batural history resolution w time
what is tracheo - oespphageal fistula
abnormal connectuon between trachea and oesophagus
majorify have associated oesophageal atresja
associagion w genetic conditions
how does a tracho oesophageal fistula oresent
choking
colour change
cough w feeding
unable to pass NG
treatment w surgical repair
what are complications w tracheo oesophageal fistula
tracheomalacia
strictures
leak
reflux
what is congenitak pulmonary airway malformation CPAM
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
what is a congenitak diaphragmatic hernia
diaphrahm sometimes doesnt close at 18 weeks or not properly
usually the left side
management is surficak repair
what is transient tachypnoea
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
what is resp dostressbsyndrome
surfactant deficiency
treated w antenatel sterouds
surfactant replacement
appropriate cent and butritoon
what is remodelling
aleteration of airway structure environmwntal exposure (smoking) chrinic diseases id childhood ( asthma) infectjon leads to abnormalities due to interference of inter cellukar signallinf
what does chrinic i flammation keas ro
increased bronchial responsiveness
incrrase mucus secretion
airway oedema
airway narrowing