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dc.contributor.authorGungor, B
dc.contributor.authorBektas, A
dc.contributor.authorAnadol, AZ
dc.contributor.authorTopgul, K
dc.contributor.authorSenyurek, G
dc.date.accessioned2020-06-21T15:29:15Z
dc.date.available2020-06-21T15:29:15Z
dc.date.issued2006
dc.identifier.issn1092-6429
dc.identifier.urihttps://doi.org/10.1089/lap.2006.16.41
dc.identifier.urihttps://hdl.handle.net/20.500.12712/20736
dc.descriptionWOS: 000235876000009en_US
dc.descriptionPubMed: 16494546en_US
dc.description.abstractPeutz-Jeghers syndrome is an infrequently encountered disease with potential complications including bleeding, intestinal obstruction, intussusception, and malignant transformation. We report on two patients, father and daughter, with Peutz-Jeghers syndrome who were admitted to hospital with similar complaints of abdominal pain. The father was 37 years old and the daughter was 17. Physical examination and laboratory tests revealed small intestinal intussusception in both patients. In the daughter, the intussuscepted segment was resected. An electrosurgical snare was also used for enteroscopic excision of multiple jejunal and ileal polyps. In the father, two 4-cm polyps were surgically resected while an enteroscopic surgical snare was used for polyps of smaller size. Both patients were discharged on postoperative day 7.en_US
dc.language.isoengen_US
dc.publisherMary Ann Liebert Incen_US
dc.relation.isversionof10.1089/lap.2006.16.41en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleEndoscopy-assisted resection for multiple polyps of the small intestine in Peutz-Jeghers syndrome: A father and daughter storyen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume16en_US
dc.identifier.issue1en_US
dc.identifier.startpage41en_US
dc.identifier.endpage44en_US
dc.relation.journalJournal of Laparoendoscopic & Advanced Surgical Techniquesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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