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14  The Oral Cavity and Gastrointestinal Tract  393

             Aetiology

             •	 Primary	 achalasia:  Aetiology  unknown  (may  be  neuronal  rather  than  a  myopathic
               disorder). Number of ganglion cells have been found to be decreased in Auerbach’s
               plexus (ganglion cell degeneration).
             •	 Secondary	forms:	Typically seen in Chagas disease (Trypanosoma cruzi infection), polio,
               diabetic autonomic neuropathy, infiltrative disorders, eg, malignancy, amyloidosis and sar-
               coidosis. Coexistence with other autoimmune diseases like Sjogren syndrome or thyroiditis
               indicates that there may be immune-mediated destruction of inhibitory oesophageal neurons.

             Microscopy
             Oesophageal wall is thickened in the distal portion (there is smooth muscle hypertrophy,
             particularly of inner circular layer); proximal dilated segment is actually thinned out.

             Q. Write briefly on gastroesophageal reflux disease (GERD).
             Ans. GERD is a chronic diffuse erosive/ulcerative oesophagitis. Normally the oesophageal
             lining is protected from acids by
               1.  The abundant submucosal glands in proximal and distal oesophagus (which secrete
                mucin and bicarbonate)
               2.  The tone of LES which prevents reflux of acidic gastric contents
             Pathogenesis

             Both genetic and environmental factors contribute to cause decreased LES pressure which
             allows reflux.

             Predisposing Factors
             Pregnancy, ascites, obesity, delayed gastric emptying and peristaltic disorders, eg, scleroderma
             Clinical Features

             Heartburn,  regurgitation,  dysphagia/odynophagia,  water  brash  (hypersalivation)  and  a
             typical intermittent chest pain
             Complications

             Ulceration, haematemesis, melena, stricture formation and Barret oesophagus

             Diagnosis
             X-ray and endoscopy

             Pathology
             •	 One-third patients have a normal appearing mucosa. Erythema and red streaks are ear-
               liest markers of disease followed by erosions and ulcers.
             •	 There may be contact bleeding with endoscope indicating increased friability.
             •	 Dilated vessels and inflammatory cells are present.
             •	 Predominance  of  eosinophils  points  to  a  diagnosis  of  ‘eosinophilic	 esophagitis’
               which  is  seen  in  patients  with  atopy  with  coexisting  atopic  dermatitis,  rhinitis,
               asthma and eosinophilia. These patients present with dysphagia and symptoms of
               food impaction.

             Q. Write briefly on Barrett’s oesophagus.
             Ans.	Barrett’s oesophagus is a complication of long-standing GE reflux. It is seen between
             40 and 60 years of age Males are more commonly affected than females. Hallmark is re-
             placement of distal squamous mucosa by metaplastic columnar epithelium as a response
             to prolonged injury.


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