1. embryology of the lungs Flashcards

1
Q

what is the respiratory diverticulum

A

blind ending outgrowth from ventral wall of foregut

forms at 4 weeks

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2
Q

what origin is the epithelial lining of the trachea, larynx, bronchi and lungs?

A

endoderm

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3
Q

how does the trachea develop?

A

4 weeks

Oesophagotracheal ridges fuse to form oesophagotracheal septum

forms from the laryngotracheal tube (layrnx too)

(respiratory diverticulum forms lungs)

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4
Q

which layers are present in the trachea during formation

A

splanchnic mesoderm-> forms cartilage, connective tissue and muscle

endoderm-> epitherlium, glands of trachea, pulomonary epithelium

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5
Q

stages of lung maturation

A

Pseudoglandular stage (5-16 weeks)

Canalicular period (16-26 weeks)

Terminal sac period (26 weeks to birth)

Alveolar period (8 months to childhood)

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6
Q

Pseudoglandular stage

A

Terminal bronchioles form

  • By the end of this period, all the major components

of the lung have formed, except those required for

gas exchange

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7
Q

how is the pleural cavity formed

A
  1. Pericardioperitoneal canals are initially connected to pericardial (primitive thoracic) and peritoneal (primitive abdominal) cavities
  2. The pericardioperitoneal canals become separated from the pericardial cavity by the pleuropericardial folds
  3. pericardioperitoneal canals (which form the pleural cavities) remain connected to the peritoneal (abdominal) cavity until closed by fusion of the pleuroperitoneal folds during formation of the diaphragm
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8
Q

Canalicular period

A

Lumens of the bronchi and terminal bronchioles enlarge

  • Tissue becomes vascularised
  • By 24 weeks, each terminal bronchiole has formed 2 or more respiratory bronchioles
  • Towards the end of this period, the first terminal sacs

form at the end of the respiratory bronchioles

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9
Q

Terminal sac period

A
  • Many terminal sacs form - the primordial alveoli
  • Epithelial cells of the terminal sacs become flat and thin - are type I alveolar epithelial cells
  • Capillaries come into close contact with the flat epithelial cells and start to bulge into the primordial alveoli. This close contact, at the blood air barrier, will allow gas exchange
  • Secretory, rounded epithelial cells start to form - are type II alveolar cells. Form in-between the flat type I alveolar cells (produce surfactant)
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10
Q

what is surfactant

A
  • Produced by type II alveolar epithelial cells
  • Phospholipid-rich fluid
  • Forms a monomolecular film over internal walls of the terminal sacs and mature alveoli
  • Lowers surface tension at the air-alveolar interface
  • Produced from the end of 6th month, though at low levels
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11
Q

Alveolar period

A

Increased production of surfactant

  • Only about 5% of mature alveoli form before birth
  • Primordial alveoli increase in size, type I epithelial cells become thinner and capillaries form an even closer association as they mature
  • Most postnatal increase in lungs size is due to increased divisions to form respiratory bronchioles and continued primordial alveoli production
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12
Q

Changes in lungs before birth

A
  • Amount of surfactant produced increases before birth, mostly in the last 2 weeks of gestation
  • Breathing movements occur before birth to stimulate lung development and respiratory muscles.
  • Amniotic fluid is aspirated
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13
Q

Changes in lungs at birth

A

at birth, lungs half filled with fluid

This fluid is removed from the lungs by:

1) Pressure on the thorax during delivery,

expelling fluid through mouth and nose

2) Absorbed into circulation via the pulmonary

circulation

3) Absorbed into lymphatics

A thin coating of surfactant is left lining the alveolar

cell membranes

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14
Q

Lungs of a stillborn

A

1st breath not taken, so no air in lungs. Lungs are full of fluid and will sink if placed in water at autopsy.

Once first breath is taken, lungs full of air and will float.

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15
Q

what is the diaphragm

A

Musculotendinous dome-shaped partition that separates the thoracic and abdominal cavities

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16
Q

four embryonic components during formation of diaphragm

A

Transverse septum

Pleuroperitoneal membranes

Dorsal mesentery of oesophagus

Muscular ingrowth from lateral body walls

17
Q

Transverse septum

A
  • Mesodermal in origin
  • Grows dorsally from ventrolateral body wall
  • Forms early in development
  • Forming liver embedded in tissue
  • Caudal to pericardial cavity – partially separating it

from peritoneal cavity

  • Primordium of central tendon of diaphragm

posterior side direct communication between peritoneal and pleuropericardial

18
Q

Pleuroperitoneal membranes

A

Form from the lateral wall of pleural and peritoneal cavities

  • First appear at the start of the 5th week
  • Forms posterior and lateral parts of diaphragm, by fusing with the transverse septum and dorsal mesentery in the 7th week
19
Q

Dorsal mesentery of oesophagus

A
  • Will form the median region of the diaphragm
  • Forms muscle bundles anterior to the aorta, the “Crura of the diaphragm”
  • Derived from myoblasts that had previously migrated into the dorsal mesentery of oesophagus
20
Q

what does the formation of primordal diaphragm occur by

A

fusion of the pleuroperitoneal membranes, dorsal mesentery of oesophagus and septum transversum. This partitions the thoracic and abdominal cavities.

21
Q

Muscular ingrowth from lateral body walls

A
  • Contributes muscle to peripheral region of diaphragm external to the region that is derived from the pleuroperitoneal membranes

occurs by 12th week

22
Q
A
23
Q

important defects and problems

A

The premature baby and Respiratory Distress Syndrome

Oesophageal atresia and tracheoesophageal fistula

Congenital cysts of the lung

Congenital diaphragmatic hernia

24
Q

what can cause respiritory distress syndrome in a premature baby

treatments

A

not enough surfactant produced- high surface tension- alveoli collapse during expiration

Treatments: Artificial surfactant and treatment with glucocorticoids to stimulate surfactant production

25
Q

Oesophageal atresia and tracheoesophageal fistulas

why can this be a problem

A

Abnormal separation of the oesophagus and trachea by the oesophagotracheal septum

most common defect of lower respiratory tract

atresia- narrowing

fistula- abnormal passage

  • Excessive amounts of fluid in mouth/ upper respiratory tract
  • Gastric contents may reflux into trachea and lungs
  • Coughing and choking
  • Pneumonia
26
Q

Congenital cysts of the lungs

A
  • Terminal bronchi abnormally dilated
  • Usually at lung periphery
  • May be small and numerous or few and large
  • Problems: drain poorly; cause chronic lung infections
27
Q

Congenital diaphragmatic hernia

A
  • Failure of fusion of pleuroperitoneal membrane with other 3 components
  • Usually a posterolateral defect
  • ~ 90% of cases are on the left side

Abdominal viscera present in thoracic cavity

  • Associated with hypoplastic lung no room for development- underdeveloped
  • Mediastinum may be pushed to the right pressure on heart