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DEVELOPMMENT OF RESPIRATORY SYSTEM

DEVELOPMMENT OF RESPIRATORY SYSTEM. Dr. Ahmed Fathalla Ibrahim. LOWER RESPIRATORY ORGANS. LARYNX TRACHEA BRONCHI LUNGS. PHARYNGEAL ARCHES. RESPIRATORY PRIMORDIUM. RESPIRATORY PRIMORDIUM. RESPIRATORY PRIMORDIUM. 6. RESPIRATORY PRIMORDIUM. Begins to form in the middle of 4 th week

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DEVELOPMMENT OF RESPIRATORY SYSTEM

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  1. DEVELOPMMENT OF RESPIRATORY SYSTEM Dr. Ahmed Fathalla Ibrahim

  2. LOWER RESPIRATORY ORGANS • LARYNX • TRACHEA • BRONCHI • LUNGS

  3. PHARYNGEAL ARCHES

  4. RESPIRATORY PRIMORDIUM

  5. RESPIRATORY PRIMORDIUM

  6. RESPIRATORY PRIMORDIUM 6

  7. RESPIRATORY PRIMORDIUM • Begins to form in the middle of 4th week • Laryngotracheal groove: a median outgrowth from the caudal end of the floor (ventral wall) of primordial pharynx, caudal to 4th pharyngeal pouch • Respiratory diverticulum: produced by deepening (evagination) of the groove, located ventral to caudal part of foregut

  8. RESPIRATORY PRIMORDIUM • Tracheal bud: it is the enlarged distal end of diverticulum • Longitudinal tracheoesophageal folds develop in diverticulum, approach each other & fuse to form tracheoesophageal septum dividing cranial part of foregut into: • Ventral part: laryngotracheal tube: primordium of larynx, trachea, bronchi & lungs • Dorsal part: pharynx, esophagus • Both parts maintain communication through primordial laryngeal inlet

  9. EMBRYOLOGICAL ORIGIN • Endoderm lining laryngotracheal tube: epithelium & glands of all respiratory organs • Fourth & sixth pharyngeal arch cartilages: all laryngeal cartilages EXCEPT epiglottis • Sixth pharyngeal arch muscles: intrinsic muscles of larynx • Mesenchyme of hypopharyngeal eminence: epiglottis • Splanchnic mesoderm surrounding foregut: connective tissue, cartilage, smooth muscles, blood & lymphatic vessels of trachea, bronchi & lungs

  10. DEVELOPMENT OF BRONCHI & LUNGS

  11. DEVELOPMENT OF BRONCHI & LUNGS • During 5th week, tracheal bud divides into 2 primary bronchial buds • Main bronchus: formed by primary bronchial bud together with its surrounding splanchnic mesoderm, divided into: secondary (lobar), tertiary (segmental) & intrasegmental branches • By 24 weeks, 17 orders of branches have formed & respiratory bronchioles have developed • After birth, 24 orders of branches are present

  12. DEVELOPMENT OF BRONCHI & LUNGS • As the lungs expand: • They invaginate pleura & acquire a visceral layer of pleura (derived from splanchnic mesoderm) • They grow caudally into body wall & lie close to heart. The thoracic body wall becomes lined by a parietal layer of pleura(derived from somatic mesoderm)

  13. MATURATION OF LUNGS • Pseudoglandular period • Canalicular period • Terminal saccular period • Alveolar period

  14. MATURATION OF LUNGS

  15. PSEUDOGLANDULAR PERIOD (6-12 WEEKS) • Lung resembles an exocrine gland • Onlybronchial & primordial terminal bronchioles are formed • Respiration is not possible

  16. CANALICULAR PERIOD (16-26 WEEKS) • Lumina of bronchi & terminal bronchioles enlarge • Respiratory bronchioles & alveolar ducts develop • Lung tissue becomes highly vascular • Respiration is possible • Fetus born at this period often dies because of immaturity of systems

  17. TERMINAL SACCULAR PERIOD (26 – BIRTH) • Alveolar ducts give rise to terminal saccules (primordial alveoli) • Terminal saccules: cuboidal epithelium begins to change into squamous • Capillaries begin to bulge into alveoli to establish blood-air barrier that permits adequate gas exchange • Terminal saccules are lined with: • Type I pneumocytes(across which gas exchange occurs): main type of cells • Type II pneumocytes(secrete surfactant)

  18. TERMINAL SACCULAR PERIOD (26 – BIRTH) Surfactant: • Role: counteracts surface tension forces & facilitates expansion of alveoli • Production: begins by 20 weeks & increases during last 2 weeks of pregnancy • By 26-28 weeks: surfactant is produced in sufficient amount for survival of prematurely born fetus

  19. ALVEOLAR PERIOD (32 WEEKS – 8 YEARS) • Number of respiratory bronchioles and terminal saccules (primordial alveoli) increases • Type I pneumocytes of terminal saccules becomes extremely thin squamous so that adjacent capillaries bulge into it • Alveolocapillary membrane is sufficiently thin to allow gas exchange

  20. ALVEOLAR PERIOD (32 WEEKS – 8 YEARS) • Lungs begin to work after birth • Transition from dependence on placenta for gas exchange to lungs requires: • Production of sufficient amount of surfactant • Development of alveolocapillary membrane that is sufficiently thin

  21. ALVEOLAR PERIOD (32 WEEKS – 8 YEARS) • Maturation of alveoli (about 95%) occurs after birth • From birth to third year: Increase in size of lungs is mostly due to increase in number of respiratory bronchioles & primordial alveoli • Immature alveoli have the potential for forming additional primordial alveoli • Immature alveoli increases in size & become mature

  22. TRACHEOESOPHAGEAL FISTULA

  23. TRACHEOESOPHAGEAL FISTULA • Most common anomaly • Associated with esophageal atresiain more than 85% of cases • Often associated with polyhydramnios • Cause: incomplete fusion of treacheoesophageal folds resulting in a defective tracheoesophageal septum & faulty partitioning of foregut into trachea & esophagus

  24. TRACHEOESOPHAGEAL FISTULA Clinical manifesttaions: • Infants cough & choke when swallowing (due to accumulation of saliva in upper respiratory tract) • Infants regurgitate when swallowing milk (milk fills esophageal pouch & is regurgitated) • Pneumonitis

  25. RESPIRATORY DISTRESS SYNDROME • Also known as hyaline membrane disease • Affects about 2% of newborn (especially premature newborn) • Cause: deficiency of surfactant • Manifestation: lungs are underinflated, alveoli contain a fluid with a high protein content that resembles a hyaline membrane

  26. RESPIRATORY DISTRESS SYNDROME • Predisposing factors: • Prolonged intrauterine asphyxia • Deficiency of thyroxine • Treatment:glucocorticoid

  27. OTHER ANOMALIES • Stenosis (narrowing) or atresia (obstruction) of trachea: due to unequal partitioning of foregut into esophagus & trachea • Congenital lung cysts: disturbance in bronchial development leads to dilation of terminal bronchi & formation of cysts filled with fluid or air • Agenesis of lung: due to failure of bronchial bud to develop

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