Right-sided Bochdalek hernia in an adult: a case report

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dc.contributor.authorUlku, Refik
dc.contributor.authorAvci, Alper
dc.contributor.authorOnat, Serdar
dc.contributor.authorOzcelik, Cemal
dc.date.accessioned2024-04-24T17:44:37Z
dc.date.available2024-04-24T17:44:37Z
dc.date.issued2011
dc.departmentDicle Üniversitesien_US
dc.description.abstractCongenital right diaphragmatic hernia of Bochdalek rarely occurs in adults. Most of them are asymptomatic. In this article, we report a case of a 21-year-old male with right-sided Bochdalek diaphragmatic hernia who presented with abdominal pain and dyspnea. The chest radiography showed features suggestive of right-sided diaphragmatic hernia. This was confirmed on a computed tomography. The patient underwent right posterolateral thoracotomy whereby a 10 cm posterolateral diaphragmatic defect with herniation of the colon and kidney through the opening was found. During surgery the colon and right kidney were reduced into peritoneal cavity, and the diaphragmatic defect was repaired with non-absorbable sutures. The patient's recovery was uneventful. He remained well at six-month follow-up.en_US
dc.identifier.endpage106en_US
dc.identifier.issn1301-5680
dc.identifier.issue1en_US
dc.identifier.startpage104en_US
dc.identifier.urihttps://hdl.handle.net/11468/22195
dc.identifier.volume19en_US
dc.identifier.wosWOS:000286413200023
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.language.isoenen_US
dc.publisherBaycinar Medical Publ-Baycinar Tibbi Yayinciliken_US
dc.relation.ispartofTurk Gogus Kalp Damar Cerrahisi Dergisi-Turkish Journal of Thoracic and Cardiovascular Surgery
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectComputed Tomographyen_US
dc.subjectDiaphragm/Diagnosis/Radiographyen_US
dc.subjectThoracic Diseases/Complication/Radiography/Surgeryen_US
dc.titleRight-sided Bochdalek hernia in an adult: a case reporten_US
dc.titleRight-sided Bochdalek hernia in an adult: a case report
dc.typeArticleen_US

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