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Duodenal atresia with apple peel associated with congenital diaphragmatic hernia: an exceptional case and a literature review. / Atresia duodenal con apple peel asociada a hernia diafragmática congénita: un caso excepcional y revisión de la literatura.
Molino Gahete, J A; López Fernández, S; Oliver, B; Boix, H; Rocha, O; López, M; Guillén, G.
Affiliation
  • Molino Gahete JA; Oncological and Neonatal Surgery Unit. Pediatric Surgery Department. Vall d'Hebrón University Hospital. Barcelona (Spain).
  • López Fernández S; Oncological and Neonatal Surgery Unit. Pediatric Surgery Department. Vall d'Hebrón University Hospital. Barcelona (Spain).
  • Oliver B; Oncological and Neonatal Surgery Unit. Pediatric Surgery Department. Vall d'Hebrón University Hospital. Barcelona (Spain).
  • Boix H; Oncological and Neonatal Surgery Unit. Pediatric Surgery Department. Vall d'Hebrón University Hospital. Barcelona (Spain).
  • Rocha O; Oncological and Neonatal Surgery Unit. Pediatric Surgery Department. Vall d'Hebrón University Hospital. Barcelona (Spain).
  • López M; Oncological and Neonatal Surgery Unit. Pediatric Surgery Department. Vall d'Hebrón University Hospital. Barcelona (Spain).
  • Guillén G; Oncological and Neonatal Surgery Unit. Pediatric Surgery Department. Vall d'Hebrón University Hospital. Barcelona (Spain).
Cir Pediatr ; 35(1): 31-35, 2022 Jan 01.
Article de En, Es | MEDLINE | ID: mdl-35037438
ABSTRACT

INTRODUCTION:

Duodenal atresia associated with apple peel is extremely rare. Duodenal atresia occurs as a result of absence of recanalization at an early stage, whereas intestinal atresia is seemingly due to vascular causes at later stages. The presence of abnormalities associated with diaphragmatic hernia is frequent, but association with duodenal atresia has been little explored. CASE REPORT This is the case of a female neonate born at gestational week 31, with duodenal atresia and apple peel, associated with left diaphragmatic hernia and major heart disease. An abdominal muscle flap was performed for diaphragmatic defect closure purposes, and duodenojejunal anastomosis was carried out following resection of part of the non-viable apple peel.

DISCUSSION:

To our knowledge, this is the first case described with this rare association. The combination of duodenal atresia and apple peel had been previously described 11 times. However, the association of both with congenital diaphragmatic hernia had not been reported yet.
RESUMEN

INTRODUCCION:

La atresia duodenal asociada con appel peel es extremadamente infrecuente. La primera se produce por un defecto en la recanalización en etapas tempranas, mientras que la atresia intestinal parece deberse a causas vasculares en etapas más tardías. La presencia de anomalías asociadas a la hernia diafragmática es común, pero la asociación con la atresia duodenal apenas está descrita. CASO CLINICO Presentamos un recién nacido de 31 semanas de gestación y sexo femenino, con atresia duodenal y apple peel, asociada a hernia diafragmática izquierda y cardiopatía mayor. Se realizó un flap muscular abdominal para el cierre del defecto diafragmático y anastomosis duodenoyeyunal tras la resección de parte del apple peel inviable.

COMENTARIOS:

A nuestro entender, es el primer caso descrito con esta asociación singular. La combinación de atresia duodenal con apple peel se ha descrito previamente en 11 ocasiones; la asociación de ambas con hernia diafragmática congénita no había sido descrita.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Malus / Occlusion duodénale / Hernies diaphragmatiques congénitales / Atrésie intestinale Type d'étude: Etiology_studies / Risk_factors_studies Limites: Female / Humans Langue: En / Es Journal: Cir Pediatr Sujet du journal: PEDIATRIA Année: 2022 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Malus / Occlusion duodénale / Hernies diaphragmatiques congénitales / Atrésie intestinale Type d'étude: Etiology_studies / Risk_factors_studies Limites: Female / Humans Langue: En / Es Journal: Cir Pediatr Sujet du journal: PEDIATRIA Année: 2022 Type de document: Article