Embryo - Respiratory System Flashcards

1
Q

What do the Coelomic clefts split into?

A

Coelomic clefts appear in the lateral plate mesoderm & split it into:

  • somatic layer (somatopleure)
    • gives rise to parietal layer of serous pericardium, pleura and peritoneum
  • splanchnic layer (splanchnopleure)
    • gives rise to visceral layer of serous pericardium, pleura and peritoneum
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2
Q

What is the result of the formation of head fold?

A
  • Pericardioperitoneal canals
    • come to sides of foregut
  • Peritoneal cavity
    • lies dorsally to sides of gut
  • Pericardial cavity
    • comes ventrical to foregut

Note:

  • 3 cavities are still continuous
  • 2 folds develop:
    • Pleuropericardial fold
    • Pleuroperitineal fold
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3
Q

What happens during formation of lateral folds?

A

A) endoderm lining inside of yolk sac

  • mesoderm surrounding outside

B) formation of intra-embryonic coelomic cavity

  • 2 lateral folds fuse to form 1 cavity
  • splits off yolk sac & leaves umbilical attachment to gut

C) Splanchnic mesoderm surrounding coelomic cavity

  • forms parietal layer evenualy
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4
Q

The pericardial, pleural & peritoneal parts form one continous coelomic canal until which week?

A

7th week!

Partitioning of the Coelomic canal:

  • Pericardio-peritoneal canals
    • lung buds grow into these
    • 2 pairs of folds are formed from lateral wall of canals
  1. Pleuropericardial folds (membranes)
    • separate pleural cavity from pericardial cavity
    • fuse w/ each other to form = fibrous pericardium
  2. Pleuroperitoneal folds (membranes)
    • separate pleural cavitities from peritoneal cavity
    • form the posterolateral part of diaphragm
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5
Q

What are the 5 major developmental components of the Diaphragm?

A
  1. Central tendon (aponeurotic)
    • forms from septum transversum
  2. Posterlateral parts
    • from pleuoperitoneal folds
  3. Peripheral part (muscular)
    • from sidewall mesenchyme (abd muscles)
  4. Crura
    • from dorsal mesentery of esophagus
    • right/left crus = attach pleura to lumbar vertebrae
  5. Musculature
    • fr_​_om C3-5 myotomes
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6
Q

What are the positional changes of the diaphragm?

A

Week 4

  • Septum transversum = near C3-5 & somite 1
    • this explains innervation of phrenic nerve

Week 8

  • Septum transversum = diaphragm is now mid-thoracic

Full-term

  • Septum transversum = diaphragm is now at L1​
    • descends due to growth on dorsal side
    • phrenic nerve descended too
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7
Q

What are the common sites of hernia through diaphragm?

A

Congenital hiatal hernia

  • esophageal hiatus = abnormally large
    • most commonly seen in adults due to:
      • chronic stress, smoking
      • weak musculature

Congenital diaphragmatic hernia

  • large posterolateral defect (pleuroperitoneal fold)
  • more common on left side
    • abdomen = empty when flat
    • abdominal contents go into thorax –> via defective hold in diaphragm
    • lung = compressed (hypoplastic)

Note:

  • 3 NORMAL openings in diaphragm:
    • Inferior Vena Cava (T8)
    • Esophagus (T10)
    • Abdoninal aorta (T12)
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8
Q

What is eventration of diaphragm?

A

Basics:

  • caused by defective musculature in 1/2 of diaphragm

Result:

  • Paradoxical Respiration
    • 1/2 diaphragm goes up w/ contraction during inspiration
  • Presents similar to congenital diaphragmatic hernia
    • hypoplasia
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9
Q

What are the 3 major structures of Respiratory primordium?

A
  1. Foregut
    • Respiratory diverticulum
      • dev. from FLOOR of the pharnyx
    • Tracheosophageal septum
      • btw. respiratory divertculum & esophagus
      • defect –> abnormal connect of trachae & esophagus
  2. Midgut
    • lateral fold –> supplied by superior mesentric a.
  3. Hindgut
    • tail fold –> supplied by inferior mesentric artery.
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10
Q

What is important about the larygotracheal tube in relation to the dervations of larnyx, trachea, bronchi components?

A

Basics:

  • cranial part –> larynx
  • LT-tube (below larynx) forms –> trachea
  • lower end of LT tube –> divides into 2 bronchial (lung buds)
    • form bronchi

Derivations of Larnyx:

  • epithelium of larynx gives rise –>
    • endodermal lining
  • laryngeal cartilages –>
    • 4th & 6th pair of pharyngeal arches
    • EXCEPT the epiglottis –>
      • dev from hypo(pharyngeal)branchial eminence
  • laryngeal muscles –>
    • mesenchyme (mesoderm) in 4th & 6th arches

Derivation of Trachea:

  • epithelial lining & glands –>
    • endoderm of LT-tube
  • CT, cartilage muscles, blood vessels –>
    • splanchnic mesoderm (surrounding LT-tube)

Derivation of Bronchi:

  • bronchial epithelium & glands –>
    • from endoderm of LT tube
  • muscles & cartilages –>
    • from surrounding splanchnic mesoderm
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11
Q

What are the 4 stages of maturation of lungs?

A
  1. Pseudoglandular (5-16 wks)
    • lung resembles compound exocrine gland
    • terminal bronchiole ONLY
      • cuboidal epithelium
  2. Canalicular (16-24 wks)
    • lumen of conducting sys enlarges
    • terminal branch –> respiratory bronchiole
      • cuboidal epithelium
    • Type II alveoli - start secreting surfactant
  3. Terminal sac (24 wks - birth)
    • respiratory –> subdivide to terminal sacs
      • cuboidal epithelium –> flat
      • associate w/ blood & lymph
  4. Alveolar (Birth - 8 yrs)
    • epithelium –> thinner (Type I pneumocytes)
    • capillaries protrude into alveolar sacs
      • form blood-air barrier
    • mature alveolus

Note:

  • if baby is born before 24th week, will likely not survive
    • poor respiratory sys development
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12
Q

What are the 3 factors important for lung development?

A
  1. Thoracic space for growth
  2. Fetal breathing movements
    • not continuous –> intermediate
    • needed for conditioning of muscles
  3. Amniotic fluid volume

Note:

  • If we do not have this, we get pulmonary hypoplasia
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13
Q

What are 3 important clinical pathologies?

A
  1. Tracheo-esophageal fistula
    • incomplete separation of laryngotracheal tube from pharynx & esophagus
    • abnormal communication w/ esophagus & trachea
  2. Respiratory Distress Syndrome (HMD)
    • aka: hyalane membrane disease
    • lack of surfactant (type II pneumocytes)
  3. Hypoplasia of the lung
    • associated w/
      • congenital diaphragmatic hernia
      • oligohydramnios ( not enough amniotic fluid)
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