A case of duodenal atresia
Abstract
Congenital atresia of the intestines and colon is an uncommon malformation in which there is complete obstruction of the alimentary tract. It rapidly produces vomiting, severe dehydration, and possibly rupture of the blind intestine. If no surgical relief is given, death supervenes in most cases in the first week of life, but surgical therapy is followed by high mortality. Prompt recognition of the obstruction and immediate operation give the only hope of survival (Gross, 1953).
Vidal (1915) as cited by Young (1966) is the first who report the successful treatment of neonatal duodenal obstruction.
References
2. GROSS, R.E.: The Surgery of Infancy and Childhood (Saunders, Philadelphia 1953).
3. SCHAFFER, A.J. : Di.8eases of The Newborn (Saunders. Philadelphia/Lon40n 1960).
4. SHACKELFORD. R.T.: Surgery of The Alimentary Tract (Saunders, Philadelphia/ London 1961).
5. SINGLETON, E.B.: X-ray Diagnosis of The Alimentary Tract in Infants and Children (Yb. Publ. Chicago 1959).
6. YOUNG, D.G. and WILKINSON, A.W.:
Mortality in Neona.tal duodenal obstruction. Lancet. ii: 2 (1966).
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Accepted 2017-03-23
Published 1973-02-28