A pancreatic pseudopapillary tumor enucleated curatively

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dc.authoridAtes, Mustafa/0000-0003-2821-453X
dc.authoridKARAKAS, SERDAR/0000-0001-8314-7806
dc.authoridErsan, Veysel/0000-0002-1510-0288
dc.authoridsoyer, haci vural/0000-0003-4271-7467
dc.authorwosidAtes, Mustafa/ABI-5100-2020
dc.authorwosidKARAKAS, SERDAR/AAB-3219-2021
dc.authorwosidErsan, Veysel/AAB-9595-2020
dc.authorwosidsoyer, haci vural/KAM-0073-2024
dc.contributor.authorKarakas, Serdar
dc.contributor.authorDirican, Abuzer
dc.contributor.authorSoyer, Vural
dc.contributor.authorKoc, Suleyman
dc.contributor.authorErsan, Veysel
dc.contributor.authorAtes, Mustafa
dc.date.accessioned2024-08-04T20:40:08Z
dc.date.available2024-08-04T20:40:08Z
dc.date.issued2015
dc.departmentİnönü Üniversitesien_US
dc.description.abstractINTRODUCTION: Pseudopapillary tumors (PPT) of the pancreas are very rare, comprising 0.3-2.7% of all pancreatic tumors, and they occur mostly in young women. Generally, they are benign, but in rare cases they can enlarge, invade adjacent organs, and metastasize distantly. Radiological assessments and biochemical markers are important for diagnosing tumor characteristics. The main treatment is tumor resection. PRESENTATION OF CASE: An 18-year-old female was referred to our department suffering from abdominal discomfort and upper quadrant abdominal pain. Abdominal computed tomography (CT) revealed a 6-x5-cm mass between the pancreatic head and right adrenal gland (Fig. 1). The histological assessment was a solid PPT of the pancreas with intact surgical borders. DISCUSSION: PPT are very rare, comprising approximately 5% of cystic pancreatic tumors and similar to 1% of exocrine pancreatic neoplasms and present mainly during the second and third decades of life. PPTs are usually indolent tumors. As such, they tend to produce vague nonspecific symptoms or may be detected incidentally on imaging. Complete surgical resection (R0) is the most effective therapy for PPT. CONCLUSION: Although PPT is a very rare, benign tumor, it has the potential to metastasize to adjacent and distant organs. Consequently, they should be detected early, so that they can be treated surgically before malignant conversion. (C) 2015 The Authors. Published by Elsevier Ltd. on behalf of Surgical Associates Ltd.en_US
dc.identifier.doi10.1016/j.ijscr.2015.03.040
dc.identifier.endpage120en_US
dc.identifier.issn2210-2612
dc.identifier.pmid25828476en_US
dc.identifier.scopus2-s2.0-84925854181en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage118en_US
dc.identifier.urihttps://doi.org/10.1016/j.ijscr.2015.03.040
dc.identifier.urihttps://hdl.handle.net/11616/96727
dc.identifier.volume10en_US
dc.identifier.wosWOS:000388734800033en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherElsevier Sci Ltden_US
dc.relation.ispartofInternational Journal of Surgery Case Reportsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPancreasen_US
dc.subjectPseudopapillaryen_US
dc.subjectEnucleationen_US
dc.titleA pancreatic pseudopapillary tumor enucleated curativelyen_US
dc.typeArticleen_US

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