Duodenal atresia Health Dictionary

Duodenal Atresia: From 1 Different Sources


a condition in which there is congenital narrowing of the duodenum causing complete obstruction. It presents at birth with vomiting, which is usually bile-stained, and is associated with other congenital abnormalities, particularly *Down’s syndrome. Treatment is by restoration of any fluid and electrolyte loss followed by surgical repair.
Health Source: Oxford | Concise Colour Medical Dictionary
Author: Jonathan Law, Elizabeth Martin

Duodenal Ulcer

This disorder is related to gastric ulcer (see STOMACH, DISEASES OF), both being a form of chronic peptic ulcer. Although becoming less frequent in western communities, peptic ulcers still affect around 10 per cent of the UK population at some time. Duodenal ulcers are 10–15 times more common than gastric ulcers, and occur in people aged from 20 years onwards. The male to female ratio for duodenal ulcer varies between 4:1 and 2:1 in di?erent communities. Social class and blood groups are also in?uential, with duodenal ulcer being more common among the upper social classes, and those of blood group O.

Causes It is likely that there is some abrasion, or break, in the lining membrane (or mucosa) of the stomach and/or duodenum, and that it is gradually eroded and deepened by the acidic gastric juice. The bacterium helicobacter pylori is present in the antrum of the stomach of people with peptic ulcers; 15 per cent of people infected with the bacterium develop an ulcer, and the ulcers heal if H. pylori is eradicated. Thus, this organism has an important role in creating ulcers. Mental stress may possibly be a provocative factor. Smoking seems to accentuate, if not cause, duodenal ulcer, and the drinking of alcohol is probably harmful. The apparent association with a given blood group, and the fact that relatives of a patient with a peptic ulcer are unduly likely to develop such an ulcer, suggest that there is some constitutional factor.

Symptoms and signs Peptic ulcers may present in di?erent ways, but chronic, episodic pain lasting several months or years is most common. Occasionally, however, there may be an acute episode of bleeding or perforation, or obstruction of the gastric outlet, with little previous history. Most commonly there is pain of varying intensity in the middle or upper right part of the abdomen. It tends to occur 2–3 hours after a meal, most commonly at night, and is relieved by some food such as a glass of milk; untreated it may last up to an hour. Vomiting is unusual, but there is often tenderness and sti?ness (‘guarding’) of the abdominal muscles. Con?rmation of the diagnosis is made by radiological examination (‘barium meal’), the ulcer appearing as a niche on the ?lm, or by looking at the ulcer directly with an endoscope (see FIBREOPTIC ENDOSCOPY). Chief complications are perforation of the ulcer, leading to the vomiting of blood, or HAEMATEMESIS; or less severe bleeding from the ulcer, the blood passing down the gut, resulting in dark, tarry stools (see MELAENA).

Treatment of a perforation involves initial management of any complications, such as shock, haemorrhage, perforation, or gastric outlet obstruction, usually involving surgery and blood replacement. Medical treatment of a chronic ulcer should include regular meals, and the avoidance of fatty foods, strong tea or co?ee and alcohol. Patients should also stop smoking and try to reduce the stress in their lives. ANTACIDS may provide symptomatic relief. However, the mainstay of treatment involves four- to six-week courses with drugs such as CIMETIDINE and RANITIDINE. These are H2 RECEPTOR ANTAGONISTS which heal peptic ulcers by reducing gastric-acid output. Of those relapsing after stopping this treatment, 60–95 per cent have infection with H. pylori. A combination of BISMUTH chelate, amoxycillin (see PENICILLIN; ANTIBIOTICS) and METRONIDAZOLE – ‘triple regime’ – should eliminate the infection: most physicians advise the triple regime as ?rst-choice treatment because it is more likely to eradicate Helicobacter and this, in turn, enhances healing of the ulcer or prevents recurrence. Surgery may be necessary if medical measures fail, but its use is much rarer than before e?ective medical treatments were developed.... duodenal ulcer

Atresia

The absence of a natural opening, or closure of it by a membrane. Thus atresia may be found in newborn infants, preventing the bowels from moving. In young girls after puberty, absence of the menstrual ?ow may be due to such a malformation at the entrance to the VAGINA.... atresia

Biliary Atresia

A rare disorder, present from birth, in which some or all of the bile ducts fail to develop or have developed abnormally.

As a result, bile is unable to drain from the liver (see cholestasis).

Unless the atresia can be treated, secondary biliary cirrhosis will develop and may prove fatal.

Symptoms include deepening jaundice, usually beginning a week after birth, and the passing of dark urine and pale faeces.

Treatment is by surgery to bypass the ducts.

If this fails, or if the jaundice recurs, a liver transplant is the only possible treatment.... biliary atresia

Duodenal Ileus

Dilatation of the DUODENUM due to its chronic obstruction, caused by an abnormal position of arteries in the region of the duodenum pressing on it.... duodenal ileus

Choanal Atresia

A congenital defect of the nose in which 1 or both of the nasal cavities are not fully developed.... choanal atresia

Tricuspid Atresia

a rare form of congenital heart disease in which there is no communication between the right atrium and the right ventricle. Affected babies present with *cyanosis, breathlessness, particularly on feeding, and *failure to thrive. Diagnosis is by *echocardiography. Treatment involves surgical intervention, but the prognosis is often poor.... tricuspid atresia

Oesophageal Atresia

A rare birth defect in which the oesophagus forms into 2 separate, blind-ended sections during development. There is usually an abnormal channel (tracheoesophageal fistula) between one of the sections and the trachea. The condition may be suspected before birth if the mother had polyhydramnios. The infant cannot swallow, and drools and regurgitates milk continually. If there is an upper tracheoesophageal fistula, milk may be sucked into the lungs, provoking attacks of coughing and cyanosis. Immediate surgery is needed to join the blind ends of the oesophagus and close the fistula. If the operation is successful, the baby should develop normally. Some babies, however, do not survive.... oesophageal atresia



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