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Association of Intestinal Malrotation and Bochdalek Hernia in an Adult: a Case Report

dc.contributor.authorSalústio, R
dc.contributor.authorNabais, C
dc.contributor.authorParedes, B
dc.contributor.authorSousa, FV
dc.contributor.authorPorto, E
dc.contributor.authorFradique, AC
dc.date.accessioned2014-05-27T14:53:49Z
dc.date.available2014-05-27T14:53:49Z
dc.date.issued2014
dc.description.abstractBackground Late presentations of congenital diaphragmatic hernia are rare and differ from the classic neonatal presentation. The association with other congenital malformations in children, mainly intestinal malrotation, is well documented. The diagnosis of this association in adults is very rare, and depends on a high degree of suspicion. Case presentation We report a case of a 50-year-old female Caucasian patient with a previous history of intestinal malrotation diagnosed in adolescence and treated conservatively. She was referred to the hospital with signs and symptoms of intestinal obstruction. The patient undertook computed tomography that confirmed small bowel obstruction with no obvious cause, and a right subphrenic abscess with right empyema was also present. An exploratory laparotomy was performed that revealed an intestinal malrotation associated with a right gangrenous and perforated Bochdalek hernia. Resection of the affected small bowel, closure of the Bochdalek foramen and the Ladd procedure were carried out. Conclusion This case shows a rare association of two rare conditions in adults, and highlights the challenge in reaching the diagnosis and management options.por
dc.identifier.citationBMC Res Notes. 2014; 7: 296.por
dc.identifier.urihttp://hdl.handle.net/10400.17/1806
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherBioMed Centralpor
dc.subjectHSJ CIRpor
dc.subjectHérnia Diafragmáticapor
dc.subjectObstrução Intestinalpor
dc.titleAssociation of Intestinal Malrotation and Bochdalek Hernia in an Adult: a Case Reportpor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage299por
oaire.citation.startPage296por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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