Giant Hiatal Hernia with Pancreas Herniation

dc.contributor.advisorAlzughayyar, Tareq Z
dc.contributor.authorAbukhalaf, Sadi A
dc.contributor.authorAmro, Adham M
dc.contributor.authorBaniowda, Muath A
dc.contributor.authorMisk, Rami A
dc.contributor.authorAbukarsh, Radwan
dc.contributor.authorGhazzawi, Ihsan
dc.contributor.authorNovotny, Nathan M
dc.contributor.authorAlzughayyar, Tareq Z
dc.date.accessioned2020-11-24T08:17:01Z
dc.date.accessioned2022-05-22T08:27:49Z
dc.date.available2020-11-24T08:17:01Z
dc.date.available2022-05-22T08:27:49Z
dc.date.issued2019-08-06
dc.description.abstractPediatric hiatal hernia is a rare congenital anomaly with congenital giant hiatal hernia being the rarest subtype. The congenital giant hiatal hernia has never been reported to contain pancreas. We report an extremely rare case of congenital giant hiatal hernia presented with respiratory distress and rapid deterioration of the respiratory function. The patient was found to have unreported intraoperative findings of colon and pancreas hiatal sac contents. Congenital giant hiatal hernia requires prompt intervention largely due to the risk of morbidity and mortality. The best option for management is surgical repair with an open or laparoscopic approach.en_US
dc.identifier.citation1en_US
dc.identifier.issn2476-1346
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/7844
dc.language.isoenen_US
dc.publisherOpen Access Journal Of Surgeryen_US
dc.subjectResearch Subject Categories::MEDICINEen_US
dc.subjectsurgeryen_US
dc.titleGiant Hiatal Hernia with Pancreas Herniationen_US
dc.typeArticleen_US

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