Respiratory System Development Flashcards

1
Q

What are fetal breathing movements?

What else is required w/ them for normal lung development?

A

priming lungs for breathing - breath in amniotic fluid
need adequate space for thoracic growth
adequate amniotic fluid volume

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2
Q

How does hyaline membrane disease present?

What causes it?

A

ground glass appearance of lungs in chest x ray

occurs bc of lack of surfactant in terminal sac stage

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3
Q

When do secondary bronchi form?

A

week 6

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4
Q

At what point do you have all your bronchopulmonary segments to the terminal bronchioles?
How many orders of branches are there?

A

24 weeks

17 orders

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5
Q

What and when happens in pseudglandular lung development?

A

5-17 weeks
terminal bronchioles formed
connective tissue from splanchnic mesoderm formed
capillaries far away from bronchioles
can’t survive if you only get to this point

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6
Q

When do primary brochial buds form?

A

week 5

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7
Q

What are the two groups of people whose lungs develop fastest?

A

african americans
females
(caucasian males develop the slowest)

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8
Q

What causes congenital diaphragmatic hernia?

What is the other name for it?

A

septum transversum and pleuroperitoneal folds do not fuse

foramen of bochdalek

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9
Q

When/what happens in alveolar development?

A

32 weeks - 8 years
alveolocapillary membrane formed
primitive alveoli start to mature - 90% of mature alveoli formed after birth
most at 3 yrs, don’t finish until 8 yrs

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10
Q

What are laryngeal webs?

A

tissue btw vocal folds = incomplete atresia
usually present in infancy w/ respiratory stress and stridor
caused by failure of recanilization

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11
Q

What canals do bronchial buds grow into?

A

pericrdial-peritoneal canals

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12
Q

When is the tracheoesophageal septum formed?

A

week 5

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13
Q

What are signs of respiratory distress in an infant?

A
tachypnea
nasal flaring
suprasternal, intercostal, or subcostal retractions
grunting
cyanosis
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14
Q

What does the primitive pharynx and respiratory diverticulum form from?

A

endoderm from 6th arch

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15
Q

What is oligohydramnios?

What does it cause?

A

too little amniotic fluid

severe cases –> retards lung development –> pulmonary hypoplasia

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16
Q

When do tertiary bronchi form?

How many are there?

A

week 7
10 right
9 left

17
Q

What is the laryngotracheal diverticulum?

A

Bud of endoderm that is the early trachea

18
Q

How many secondary bronchi are there?

A

3 on right: superior, middle, inferior

2 on left: superior, inferior

19
Q

Oligohydramnios at what stage significantly increases risk of pulmonary hypoplasia?

A

oliogohyramnios prior to 26 weeks

20
Q

When/what happens in canalicular lung development?

A

16-25 weeks
vessels are much closer to terminal sacs now
primordial alveolar ducts have formed from respiratory bronchioles –> terminal sacs
can survive w/ medical intervention

21
Q

What is laryngomalacia?

A

collapse of the supraglottic structures during inspiration = most common congenital anomaly of the larynx
mechanism unknown

22
Q

How does congenital diaphragmatic hernia present?

A

will see intestines in thorax w/ heart pushed over to the right
barrel-shaped thorax
abdomen scaphoid shaped
absence of breath sounds ipsilaterally

23
Q

What is recanalization and when does it occur in the larynx?

A

sequence of apoptosis that allows the endodermal proliferation to turn into a tube again –> allows for laryngeal ventricals and vocal and vestibular folds
10th week

24
Q

When is surfactant detectible in amniotic fluid?

A

starting at week 25

25
Q

How many arytenoid swellings are there?

A

1, 2, 3, 4, 5 disappears, 6

26
Q

What is the hypobranchial eminence?

A

comes from arytenoid arch 4 –> turns into epiglottis

27
Q

What are the tracheoesophageal folds and septum?

A

folds are the first bit of endoderm that separate the growing trachea and esophagus (coronal plane) –> once grown together = tracheoesophageal septum

28
Q

What is laryngeal atresia?

A

failure of recanilization –> larynx is completely closed

29
Q

What is the most common kind of tracheoesophageal fistula?

A

esophageal atresia = blind end esophagus

84% of cases are this

30
Q

What are the 2 types of Tracheoesophageal fistula?

A

esophageal atresia = blind end esophagus

trachoesophageal fistula = abnormal passage btw trachea and esophagus

31
Q

What are the arytenoid swellings made of?

What do they turn into?

A

neural crest covered in endoderm

turn into cartilage

32
Q

What neonatal condition can be a risk factor for TE fistula?

A

polyhydramnios (too much amniotic fluid)

33
Q

What general part of the lung forms first?

A

superior part

34
Q

When/what happens in terminal sac lung development?

A
24 weeks - birth
type I and II pneumocytes differentiate 
surfactant now produced
lymphatic capillaries developed
will survive
35
Q

How is intra-alveolar fluid cleared at birth?

A

by pressure on thorax during vaginal delivery –> out mouth and nose
into pulmonary capillaries, arteries, and veins
into lymphatics

36
Q

What are congenital lung cysts filled with?

Why do we think they form?

A

air or fluid - looks like honeycomb on x ray

thought to be bc of disturbance in bronchial dev during late fetal life

37
Q

What causes a TE fistula?

When would it occur?

A

problem w/ tracheal esophageal folds

week 5

38
Q

What are the 4 stages of lung development?

A
  1. pseudoglandular (5-17 weeks)
  2. canalicular (16-25 weeks)
  3. terminal sac (24 weeks - birth)
  4. alveolar (32 weeks - 8 years)