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BMJ 2006;332:1438 (17 June), doi:10.1136/bmj.332.7555.1438
Mark Fox, specialist registrar1, Alasdair Young, senior house officer2, Roy Anggiansah, physiologist1, Angela Anggiansah, director1, Jeremy Sanderson, consultant2
1 Oesophageal Laboratory, St Thomas' Hospital, London SE1 7EH, 2 Department of Gastroenterology, St Thomas' Hospital
Correspondence to: MFox markfox{at}doctors.org.uk
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Kenneth Neville is a 22 year old student who presented to his general practitioner at the age of 18 with regurgitation and vomiting after meals. These symptoms became a recurrent problem, but laboratory investigations including full blood count and renal and liver function tests gave normal results. As a child Mr Neville had had frequent chest infections. His mother had been very concerned about his health and often took him to the doctors. He had reflux disease and asthma diagnosed. His asthma remains difficult to control despite the use of inhalers, sodium cromoglicate, and leukotriene receptor antagonists. Nevertheless, he completed school with good qualifications and was happy at college, achieving good grades. He was president of his class and organised events. He did not smoke, drink excessive alcohol, or take drugs. He had no relevant family medical history.
When he was 21, Mr Neville was admitted to his local hospital for two months with severe nausea, epigastric pain, regurgitation, and vomiting. Routine investigations, including a malabsorption screen, tests for thyroid function and coeliac disease autoantibodies, and abdominal ultrasonography and upper gastrointestinal endoscopy, did not find a cause. Manometry showed normal peristaltic function (figure), but pH studies showed severe oesophageal exposure to acid (table). He had gastro-oesophageal reflux disease diagnosed and started treatment with acid suppressing and prokinetic drugs (omeprazole 20 mg twice daily, domperidone 10 mg four times a day). This management eased the abdominal pain but did not relieve the other symptoms. He was discharged despite strong objections.
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Mr Neville's condition was stable over the summer but his symptoms caused increasing difficulties on his return to college. After a difficult meeting with a member of staff he withdrew from classes. His condition deteriorated further and he was admitted for a second time on new year's eve. His postprandial regurgitation and vomiting were more severe, adequate oral intake was impossible, and he was losing weight. He complained of generalised weakness, abdominal pain, and constipation. On examination he was thin but had no anaemia, lymphadenopathy, or other signs of systemic disease. His cardiac and respiratory function was normal and an abdominal examination showed faecal loading. Routine laboratory tests and plain chest and abdominal radiographs provided no evidence of electrolyte disturbance, malabsorption, infection, inflammation, or malignancy.
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(Accepted 5 January 2006)
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