Terminal Ileum Angiolipoma Prolapsing through the Ileocecal Valve into the Colon Causing Symptoms of Intermittent Subileus: A Rare Case Report

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dc.authoridÖzel, A.Melih/0000-0003-3374-3997en_US
dc.authoridMidi, Ahmet/0000-0002-6197-7654en_US
dc.authoridSezgin, Gülbüz Güler/0000-0002-0774-2766en_US
dc.authoridMidi, Ahmet/0000-0002-6197-7654en_US
dc.contributor.authorYener, Neşe Arzu
dc.contributor.authorSezgin, Gülbuz
dc.contributor.authorManukyan, Manuk
dc.contributor.authorMidi, Ahmet
dc.contributor.authorÖzel, Ahmet Melih
dc.contributor.authorBayramicli, Oya Uygur
dc.date.accessioned2024-07-12T21:37:44Z
dc.date.available2024-07-12T21:37:44Z
dc.date.issued2014en_US
dc.department[Belirlenecek]en_US
dc.description.abstractAngiolipoma is a common benign neoplasm of subcutaneous tissues and it is rarely located in the gastrointestinal tract. We report an 86-year-old woman with ileal angiolipoma having the symptoms of intermittent subileus without any significant laboratory findings. We focus on the correct pre- and postoperative diagnosis of this rare entity at this rare localization.en_US
dc.identifier.doi10.5152/imj.2014.30301
dc.identifier.endpage62en_US
dc.identifier.issn1304-8503
dc.identifier.issn2148-094X
dc.identifier.issue1en_US
dc.identifier.startpage60en_US
dc.identifier.urihttps://doi.org/10.5152/imj.2014.30301
dc.identifier.urihttps://hdl.handle.net/20.500.12415/6912
dc.identifier.volume15en_US
dc.identifier.wosWOS:000421117200017en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Science
dc.language.isoenen_US
dc.publisherAvesen_US
dc.relation.ispartofIstanbul Medical Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.snmzKY04254
dc.subjectTerminal Ileum Angiolipomaen_US
dc.subjectAngiolipomaen_US
dc.subjectAngiolipoma Of The Small Intestineen_US
dc.titleTerminal Ileum Angiolipoma Prolapsing through the Ileocecal Valve into the Colon Causing Symptoms of Intermittent Subileus: A Rare Case Reporten_US
dc.typeArticle
dspace.entity.typePublication

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