Oesophageal anatomy

Germ Cell layers

  • Endoderm
    • Epithelial lining and glands
  • Mesoderm
    • Lamina propria, muscularis mucoase, submucosa, muscularis externa, serosa
  • Ectoderm
    • Enteric nervous system, posterior luminal digestive structures

Primitive gut tube

  • Foregut, midgut, hindgut
    • Oesophagus from foregut
  • Formation from infoldings
    • Incorporation of endoderm into primitive gut tube
    • Cranial and caudal end form blind ending tube
  • Middle part remains connected to yolk sac by vitelline duct

Epithelium

  • Proliferation of epithelial lining of gut tube
    • Lumen obliterated by week 6
  • Central cells then degenerate
    • Tube recanalized by week 8
    • Abnormalities in this process lead to
      • Stenosis
      • Atresia
      • Duplication cysts

Oesophagus and Lung Development

  • During 4th week
  • Respiratory tract forms from a ventral bud from pharynx
    • Lateral grooves invaginate on each side and fuse to create tracheooesophageal septum, making two distinct tubes
    • Septum separates respiratory and digestive tracts
      • Failure leads to tracheo-oesophageal fistula

Growth of Oesophagus

  • Initially short
  • Rapidly elongates, due to lung development and heart descent
  • Final position by week 7
  • Failure to lengthen
    • Short oesophagus and congenital hiatus hernia

Oesophageal Wall Development

  • Upper part
    • Striated muscle
    • Striated muscle and upper oesophageal sphincter derived from mesenchyme of Branchial Arches 4,5,6
    • Explains upper oesophageal sphincter innervation
      • Vagus – nerve of Branchial Arch 5
      • Recurrent Laryngeal – nerve of Branchial Arch 6
  • Middle part
    • Mixed
  • Lower part
    • Smooth muscle
    • From Splanchnic Mesoderm
    • Lower oesophageal sphincter innervated both by
      • Parasympathetic – Vagus
      • Sympathetic – Mostly Splanchnic N

Congenital Anomalies

  • Rare – 1/3000-5000
  • Oesophageal atresia
    • Failure of recannalisation
  • Tracheo-oesophageal fistulae
    • Failure of lateral invaginations
  • Stenosis, Web, Muscular Hypertrophy
    • Abnormal recannalisation
  • Duplication Cysts