Simultaneous correction of esophageal and duodenal atresia in a newborn: A clinical case
DOI:
https://doi.org/10.37800/RM.4.2023.86-90Keywords:
esophageal atresia (EA), duodenal atresia (DA), newborn, combined gastrointestinal tract (GIT) malformationAbstract
Relevance: Esophageal atresia (EA) and duodenal atresia (DA) are complex malformations of the gastrointestinal tract (GIT) that require surgical treatment. The combination of these two malformations is quite rare (in 3-6% of newborns with EA) and there is not sufficient medical experience in pediatric surgery in treating such patients.
The study aimed to present a clinical case of simultaneous correction of a combined malformation of the GIT, as an example of an algorithm for the interaction of various specialists in one-stage surgical correction of EA and DA in a newborn.
Materials and Methods: The study describes a clinical case of simultaneous surgical correction of EA and DA in a newborn who was treated at the National Research Center for Maternal and Child Health “UMC”, (Astana, Kazakhstan) in 2020.
Results: There is a positive outcome of a one-stage method for correctiing EA and DA in the described clinical case, considering the stable condition of the newborn patient.
Conclusion: Due to the pediatric surgery and nursing technology development, one-stage correction of gastrointestinal malformations in newborns with a good treatment outcome has become possible. The presented case is described to increase the clinical awareness of the pediatric surgical community regarding the outcome of one-stage surgical treatment in similar pathologies.
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