Embryology (respi) Flashcards

(36 cards)

1
Q

Stages of respi development (earliest to latest)

A

Embryonic

Pseudoglandular

Canalicular

Saccular

Alveolar

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2
Q

What is a lung bud/respiratory diverticulum?

A

Outpouching of developing foregut region

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3
Q

What is necessary for functional stability?

A

Separation btw developing foregut and respiratory diverticulum

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4
Q

Main origins for development of respi structures

A

Gut tube

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5
Q

Fn of tracheoesophageal septum?

A

Separates trachea and esophagus

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6
Q

What envelopes tracheoesophageal septum?

A

Mesoderm

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7
Q

What facilitates separation of trachea and esophagus during fetal development?

A

Emergence of tracheoesophageal folds

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8
Q

How is tracheoesophageal septum formed?

A

Fusing of tracheoesophageal folds in midline

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9
Q

What complication arises if separation doesn’t occur completely?

A

Fistula

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10
Q

How is bronchial bud formed?

A

Respiratory diverticulum bifurcates into right and left bud

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11
Q

What does the bronchial bud turn into later on during development?

A

Pri bronchi

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12
Q

When does formation of tertiary bronchi occur?

A

End of embryonic stage

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13
Q

What happens during the pseudoglandular stage?

A

Formation of more intricate structures of the respi sys

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14
Q

What is the canalicular stage?

A

Specialised development of respi component within lung themselves

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15
Q

What happens during canalicular stage?

A

Terminal bronchioles -> respiratory bronchioles -> alveolar ducts -> alveolar sacs

Formation of canals and widening of canals

Increased vascularisation and respi bronchioles -> influx of pulmonary capillaries

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16
Q

What is an acinus?

A

Unit consisting of terminal bronchioles, alveolar duct, terminal sac

Immature precursor to the final alveoli

17
Q

Is a foetus able to survive it is born premature during the canalicular stage?

A

Yes, some alveoli capable of supporting gas exchange

18
Q

What happens during the saccular stage?

A

Alveolar ducts -> alveolar sacs

19
Q

Type 1 vs type 2 alveolar cells

A

Type 1
- flat and thin
- needed for gas exchange

Type 2
- produce surfactant -> reduce surface tension of fluid in lungs to prevent collapse of alveoli

20
Q

What happens during the alveolar stage?

A

Proliferation and maturation of alveoli

Continuous increase in vascularisation -> increase in pulmonary capillaries surrounding each alveoli

21
Q

Describe blood circulation during fetal life

A

Lungs filled w/ fluid -> alveoli collapsed

Pulmonary vascular resistance high

Heart has shunts to bypass lungs because fetus is receiving oxygenation from placenta

22
Q

How does babies’ circulation change at birth?

A

Baby take breath -> lungs fill w/ air and pulmonary vascular resistance drops
- cardiac shunts close -> blood flows through lungs

23
Q

Components of developing diaphragm

A

Somites (muscles for diaphragm), septum transversum and pleuroperitoneal folds

24
Q

What happens if diaphragm is not fully formed?

A

Abdominal content herniate into thoracic cavity (congenital diaphragmatic hernia)

25
What is a fistula?
Abnormal connection btw 2 hollow spaces
26
What is esophageal atresia?
Narrowing/closure of adjacent esophagus
27
Manifestations of tracheoesophageal fistula
Failure to thrive Aspiration/lung infection Polyhydramnios - fetus can't swallow amniotic fluid -> excess amniotic fluid in womb
28
Signs that a baby has tracheoesophageal fistula
GIT distended w/ air -> air go into esophagus instead of trachea Feeding tube doesn't extend to stomach as it's caught in proximal oesophagus
29
How to treat tracheoesophageal fistula?
Surgical repair
30
What does newborn respiratory distress syndrome/hyaline membrane disease occur?
Occurs due to insufficient surfactant production in immature lung of premature infants
31
Clinical features of newborn respiratory distress syndrome
Breathing in rapid and laboured manner Indrawing of infant's ribcage -> use of accessory respiratory muscles to generate high intrathoracic pressure to expand poorly compliant lung Cyanosis -> blue and purple discolouration of skin
32
Features of an X-ray of an infant w/ respiratory distress syndrome
Decreased lung vol Increased patchiness of lung
33
Management of newborn respiratory distress syndrome
Surfactant therapy Antenatal corticosteroids -> accelerate fetal lung development and surfactant production Continuous positive airway pressure (CPAP)
34
What is congenital diaphragmatic hernia?
Failure of normal closure of the pleuroperitoneal membrane
35
Clinical features of congenital diaphragmatic hernia
Structures displaced to one side Scaphoid abdomen Absent breath sounds
36
Management of congenital diaphragmatic hernia
Surgical repair