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• Congenital conditions of the oesophagus
• Laryngo-tracheal-oesophaeal clefts/Congenital
tracheo-oesophageal fistula
• Congenital oesophageal atresia
• Congenital stricture
• Congenital hiatus atresia
• Dysphagia lusoria
• Congenital tracheo-oesophageal fistula
• Laryngo-tracheo-oesophagial fistula results from the
fusion failure of the lateral furrows that creates the
tracheao-oesophageal septum during the 5th & 7th
week
• There are four types
• Type –I fistula: or complete oesophageal atresia
• Upper and lower oesophagus both end in blind
pouches
• Type-II fistula: the upper oesophageal end
communicates with the trachea and the lower segment
ends in a blind segment
• Type-III fistula: the upper oesophageal ends in a blind
segment and the lower segment communicates with
the trachea
• Type-IV fistula: the upper oesophageal segment and
the lower segment communicates with the trachea
• Symptoms:
• Seen immediately after birth
• Infant has barking cough with choking and cyanosis
which increases on feeding. Features of broncho-
pneumonia due to aspirationare often present
• Investigations:
• Endoscopy
• Treatment:
• Stabilisation of respiratory function by either
endotracheal intubation or tracheostomy
• Definitive treatment: Surgical repair
• Traumatic conditions of the oesophagus
• Burns & scalds
• Trauma due to foreign bodies
• Trauma due to external injuries
• Symptoms:
• Pain
• Dysphagia
• Features of shock
• Investigations:
• Endoscopy
• Neurological conditions of the oesophagus
• Cricopharyngeal spasm
• Achalasia cardia
• Primary oesophageal motility disorder associated with
the spasm of the lower oesophageal sphincter due to
neuromuscular inco-ordination
• Symptoms:
• Affects males and females equally
• Initial symptoms is retrosternal fullness
• Dysphagia is a late symptom
• Investigation:
• Ba swallow
• Endoscopy
• Treatment:
• Smooth muscle relaxants : isosorbide dinitrite
• & Ca channel blockers like verapramil,
diltiazem
• Surgical:
• Balloon dilatation
• Heller’s cardiomyotomy

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  • 1. • Congenital conditions of the oesophagus • Laryngo-tracheal-oesophaeal clefts/Congenital tracheo-oesophageal fistula • Congenital oesophageal atresia • Congenital stricture • Congenital hiatus atresia • Dysphagia lusoria
  • 2. • Congenital tracheo-oesophageal fistula • Laryngo-tracheo-oesophagial fistula results from the fusion failure of the lateral furrows that creates the tracheao-oesophageal septum during the 5th & 7th week • There are four types • Type –I fistula: or complete oesophageal atresia • Upper and lower oesophagus both end in blind pouches • Type-II fistula: the upper oesophageal end communicates with the trachea and the lower segment ends in a blind segment • Type-III fistula: the upper oesophageal ends in a blind segment and the lower segment communicates with the trachea
  • 3. • Type-IV fistula: the upper oesophageal segment and the lower segment communicates with the trachea • Symptoms: • Seen immediately after birth • Infant has barking cough with choking and cyanosis which increases on feeding. Features of broncho- pneumonia due to aspirationare often present • Investigations: • Endoscopy • Treatment: • Stabilisation of respiratory function by either endotracheal intubation or tracheostomy • Definitive treatment: Surgical repair
  • 4. • Traumatic conditions of the oesophagus • Burns & scalds • Trauma due to foreign bodies • Trauma due to external injuries • Symptoms: • Pain • Dysphagia • Features of shock • Investigations: • Endoscopy
  • 5. • Neurological conditions of the oesophagus • Cricopharyngeal spasm • Achalasia cardia • Primary oesophageal motility disorder associated with the spasm of the lower oesophageal sphincter due to neuromuscular inco-ordination • Symptoms: • Affects males and females equally • Initial symptoms is retrosternal fullness • Dysphagia is a late symptom • Investigation: • Ba swallow • Endoscopy
  • 6. • Treatment: • Smooth muscle relaxants : isosorbide dinitrite • & Ca channel blockers like verapramil, diltiazem • Surgical: • Balloon dilatation • Heller’s cardiomyotomy