Omphalocele with intestinal prolapse through a patent omphalomesenteric duct: A case report
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作者:
Sandifer, Sarapettey
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Penn State Univ, Coll Med, State Coll, PA USAPenn State Univ, Coll Med, State Coll, PA USA
Sandifer, Sarapettey
[1
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Kulaylat, Afif N. .
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Penn State Hlth Milton S Hershey Med Ctr, Div Pediat Surg, Hershey, PA USAPenn State Univ, Coll Med, State Coll, PA USA
Kulaylat, Afif N. .
[2
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Mola, Sara
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Penn State Hlth Milton S Hershey Med Ctr, Div Neonatol, Hershey, PA USAPenn State Univ, Coll Med, State Coll, PA USA
Mola, Sara
[3
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Fahy, Aodhnait S.
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Penn State Hlth Milton S Hershey Med Ctr, Div Pediat Surg, Hershey, PA USA
Penn State Hlth Milton S Hershey Med Ctr, Div Gastroenterol & Hepatol, 500 Univ Dr, Hershey, PA 17033 USAPenn State Univ, Coll Med, State Coll, PA USA
Fahy, Aodhnait S.
[2
,4
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机构:
[1] Penn State Univ, Coll Med, State Coll, PA USA
[2] Penn State Hlth Milton S Hershey Med Ctr, Div Pediat Surg, Hershey, PA USA
[3] Penn State Hlth Milton S Hershey Med Ctr, Div Neonatol, Hershey, PA USA
[4] Penn State Hlth Milton S Hershey Med Ctr, Div Gastroenterol & Hepatol, 500 Univ Dr, Hershey, PA 17033 USA
Introduction: The combination of a patent omphalomesenteric duct in the setting of an omphalocele is rare and has an unusual physical appearance on presentation.Case presentation: We share the case of a neonate who presented with omphalocele and a concurrent patent omphalomesenteric duct with intestinal prolapse. We report the early diagnosis and operative management of this presentation with intestinal resection and anastomosis, and primary closure of the omphalocele. The patient had no other abnormalities and after uncomplicated recovery, was able to discharge uneventfully tolerating oral feeds. Conclusion: Because the initial appearance of a patent omphalomesenteric duct in an omphalocele is unusual with visible bowel mucosa and an intact omphalocele membrane, this variation of an abdominal wall defect is at risk of being misdiagnosed as a ruptured omphalocele, gastroschisis, or another complex abdominal wall defect. Expeditious surgical management is indicated.