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Inflammatory Myofibroblastic Tumor: a Rare Cause of Invagination in Adults

dc.authorid Peksen, Caghan/0000-0003-3956-6282
dc.authorid Yilmaz, Ozkan/0000-0001-7320-0722
dc.authorscopusid 24335444000
dc.authorscopusid 55998916900
dc.authorscopusid 55991052400
dc.authorscopusid 57094191100
dc.authorwosid Pekşen, Çağhan/Aat-3084-2020
dc.contributor.author Kiziltan, Remzi
dc.contributor.author Yilmaz, Ozkan
dc.contributor.author Almali, Necat
dc.contributor.author Peksen, Caghan
dc.date.accessioned 2025-05-10T17:58:10Z
dc.date.available 2025-05-10T17:58:10Z
dc.date.issued 2016
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Kiziltan, Remzi; Yilmaz, Ozkan; Almali, Necat] Training & Res Hosp, Dept Gen Surg, Van, Turkey; [Kiziltan, Remzi; Yilmaz, Ozkan; Peksen, Caghan] Yuzuncu Yil Univ, Sch Med, DursunOdabas Med Ctr, Dept Gen Surg, Van, Turkey en_US
dc.description Peksen, Caghan/0000-0003-3956-6282; Yilmaz, Ozkan/0000-0001-7320-0722 en_US
dc.description.abstract Inflammatory myofibroblastic tumor (IMT) is a distinct pseudosarcomatous lesion arising in the soft tissues and interior organs of children and young adults. It is rarely seen in adults. It was first described in lungs. IMT can occur in any location in the body. However, it is seen most commonly in lungs, intestinal mesentery and liver. Non-mesenteric alimentary tract IMT's are quite rare. The presented case is an ileal IMT that caused small bowel invagination. A 38 year-old male patient presented to the emergency department with the complaint of diffuse abdominal pain, distension and no passage of gas or stools for two days. An abdominal examination revealed distension and tenderness in the abdomen with no guarding or rebound tenderness. Computerized tomography (CT) of the abdomen was ordered. CT revealed an image compatible with invagination of the right lower quadrant of the abdomen and a mass inside the lumen measuring 4x3x3cm. The mass causing invagination was detected during the surgical operation. A segmentary small bowel resection and ileoileal anastomosis was performed. The patient was discharged uneventfully on the postoperative sixth day. The diagnosis of IMT was confirmed histologically and immunochemically. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.12669/pjms.321.9326
dc.identifier.endpage 262 en_US
dc.identifier.issn 1682-024X
dc.identifier.issue 1 en_US
dc.identifier.pmid 27022387
dc.identifier.scopus 2-s2.0-84956945945
dc.identifier.scopusquality Q1
dc.identifier.startpage 260 en_US
dc.identifier.uri https://doi.org/10.12669/pjms.321.9326
dc.identifier.uri https://hdl.handle.net/20.500.14720/20298
dc.identifier.volume 32 en_US
dc.identifier.wos WOS:000369318000055
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher Professional Medical Publications en_US
dc.relation.ispartof Pakistan Journal of Medical Sciences en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Inflammatory Myofibroblastic Tumor (Imt) en_US
dc.subject Invagination en_US
dc.subject Adult en_US
dc.subject Ileus en_US
dc.title Inflammatory Myofibroblastic Tumor: a Rare Cause of Invagination in Adults en_US
dc.type Article en_US

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