Embryology 3 Flashcards

1
Q

what does the tubular outgrowth from foregut (oesophagus) develop into?

A

the trachea and lung buds

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2
Q

what happens when the lung buds proliferate?

A

they will invaginate laterally into the pleural cavities, so forming visceral and parietal pleura and the pleural cavity

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3
Q

how is the diaphragm formed

A

whilst the parts of the trachea and lungs are forming a transverse septal ‘shelf’ develops between thorax and abdomen below the pleural cavities

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4
Q

what is the septal ‘shelf’ composed of

A

4 components that fuse to form the diaphragm

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5
Q

how do congenital abnormalities come about?

A

things can go wrong with the embryonic tracheal, lung and diaphragmatic formation

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6
Q

what does folding of the embyro during week 3 give rise to?

A

the primitive gut tube

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7
Q

what comes from the midgut and hindgut

A

gut

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8
Q

what comes from the ventral wall of the foregut

A

trachea and lungs

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9
Q

when does tracheal and lung development start

A

4 weeks gestation

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10
Q

how does the trachea start to develop

A

a median outgrowth called the laryngotracheal groove from the ventral part of the foregut

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11
Q

how do the trachea and oesophegus separate

A

oesophagotracheal septum - that completely separates them into trachea ventrally and oesophagus dorsally - a relationship that is maintained into adulthood.

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12
Q

what is Tracheoesophageal fistula

A

A fistula is an abnormal connection or passageway that connects two organs or vessels that do not usually connect
TOF is a common congenital abnormality.

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13
Q

Define atresia

A

a condition in which a passage in

the body is closed or absent (abnormal to usual anatomy)

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14
Q

lining of the thoracic wall

A

becomes lined by a layer ofparietal pleura, derived from somatic mesoderm

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15
Q

what is the gap between the parietal and visceral pleurae called

A

called pleuroperitoneal canals - these eventually become the pleural canals

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16
Q

during lung development, when are the alveolar sacs formed?

A

during 27-40 week period

alveolar sacs will be progressively divided into smaller subunits leading to the formation of alveoli later on

17
Q

what is respiratory distress syndrome (RDS)

A
  • acute lung disease caused by surfactant deficiency, which leads to alveolar collapse and noncompliant lungs (underdeveloped lungs basically)
  • Affects 2 % of neonates
18
Q

what does the septum transversum become in the diagphragm

A

the central tendon

19
Q

what do the pleuroperitoneal membranes become

A

the primitive diaphragm

20
Q

what does the dorsal mesentery of oesophagus become

A

the median portion and crura (leg shaped tendons) of the diaphragm

21
Q

which embryonic components make up the peripheral parts of diaphragm

A

muscular ingrowth from lateral body walls

22
Q

what 4 embryonic components develop into the diaphragm

A

Septum transversum Pleuroperitoneal membranes
Dorsal mesentery of oesophagus
Muscular ingrowth from lateral body walls

23
Q

where is the septum transversum initially located?

A

opposite C3-C5 somites

it migrates caudally

24
Q

3 major congenital defects during diaphragm development

A

Failure of the diaphragm to completely close during development

Herniation of the abdominal contents into the chest

Pulmonary hypoplasia

25
Q

define hernia

A

bulge or protrusion of an organ through the structure or muscle that usually contains it.

26
Q

what 3 types of diaphragmatic herniae can you get?

A
  1. posteriolateral (Bochdalek) hernia
  2. anterior (Morgagni) hernia
  3. central hernia
27
Q

what 2 types of hiatal herniae can you get

A

a hernia through the holes in the diaphragm

  1. sliding hiatus hernia
  2. paraesophageal hiatus hernia ‘rolling’ hiatus hernia