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dc.contributor.authorRizalar R.
dc.contributor.authorSomuncu S.
dc.contributor.authorSözübir S.
dc.contributor.authorYildiz L.
dc.contributor.authorGürses N.
dc.date.accessioned2020-06-21T09:19:39Z
dc.date.available2020-06-21T09:19:39Z
dc.date.issued1996
dc.identifier.issn0019-5456
dc.identifier.urihttps://doi.org/10.1007/BF02905736
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3105
dc.descriptionPubMed: 10832480en_US
dc.description.abstractDuplications of the alimentary tract are rare congenital anomalies that mayoccur at any level from mouth to anus. While the oesophagus and the ileum are the most common sites, duplications of the colon are rare. Two cases of ileocolic intussusceptions in 8-month-old girl and 6-month-old boy who were admitted to our hospital with acute abdomen findings are presented. Intraoperatively, cecal cystic duplications leading intussuception were revealed. Intussusception is one of the most important surgical emergence in infancy and typically, it does not involve a lead point in childhood. Although duplication cyst may act as lead point, the review of literature reveals its rarity. © 1996 Dr. K C Chaudhuri Foundation.en_US
dc.language.isoengen_US
dc.publisherSpringer Indiaen_US
dc.relation.isversionof10.1007/BF02905736en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCecalen_US
dc.subjectDuplication cysten_US
dc.subjectintussuceptionen_US
dc.titleCecal duplications : A rare cause for secondary intussusceptionen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume63en_US
dc.identifier.issue4en_US
dc.identifier.startpage563en_US
dc.identifier.endpage566en_US
dc.relation.journalThe Indian Journal of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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