2006, Number 1
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Rev Mex Cir Pediatr 2006; 13 (1)
Prenatal Diagnosis: Jejunal Atresia Special Solution: A Team Miltidisciplinario
Milan-Montenegro JG, Salazar-Chavira JL, Hernández-Flores JG, Arizpe-Gutierrez A, Gonzalez-Ortega S
Language: Spanish
References: 20
Page: 39-43
PDF size: 375.52 Kb.
ABSTRACT
Introduction: Proceeding with prenatal diagnosis of congenital malformations, is a reality, even more, when the kid’s mother presents polhidramnios in prenatal control and where an ecosonogram permitted us to diagnose the Yeyuno Atresia, always counting on help from a first class private hospital, where we performed complete treatment to obtain a good quality of life for the child.
Clinical Case: Premature membrane rupture of 37 year old first child mother, led us to cesarea; immediately confirmed by clinical and X rays diagnosis. Proceeded with surgery 16 minutes after born, identifying Yeyuno Atresia type III b with separated ends, “Apple peel” mesentery and intestinal malrotation. Post surgery evolution: 8 days without food, TPN*, got rid of oral tubes, fed orally up to maternal milk.
Conclusions: Pregnant pacient with polhidramnios requires abdominal ecosonogram to diagnose digestive tube malformation, which has to be confirmed at N/B leading to immediate surgery with special medical equipment as well as a specialized surgery team. We recommend the applied technique, with a complete involvement from a Neonatologist in NICU**, total parenteral nutrition in first class hospital that will contribute in obtaining excellent results.
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