Publication:
Solid pseudopapillary tumor of the pancreas: a rare entity

dc.contributor.authorsKaradeniz-Cerit, Kivilcim; Ergelen, Rabia; Kalyoncu, Aybegum; Toper, Hasan; Dagli, Tolga E.
dc.date.accessioned2022-03-13T12:44:47Z
dc.date.accessioned2026-01-11T17:49:57Z
dc.date.available2022-03-13T12:44:47Z
dc.date.issued2014
dc.description.abstractSolid pseudopapillary tumor (SPT) of the pancreas is a rare neoplasm in children that mainly occurs in young females. We herein report a rare case of SPT arising from the tail of the pancreas. A 13-year-old girl was admitted to our clinic with abdominal pain and anorexia. A mass was palpated on the physical examination. A 90x72 mm, encapsulated, heterogeneous mass with solid and cystic components was defined on computerized tomography (CT). Distal pancreatectomy was performed during the operation. Histopathological examination revealed that the tumor was a SPT with negative surgical margins. A six-month follow-up after surgical resection showed no evidence of recurrent disease. SPT should always be considered in the differential diagnosis in a young female with a palpable mass.
dc.identifier.doidoiWOS:000345957300017
dc.identifier.issn0041-4301
dc.identifier.pubmed25341607
dc.identifier.urihttps://hdl.handle.net/11424/237650
dc.identifier.wosWOS:000345957300017
dc.language.isoeng
dc.publisherTURKISH J PEDIATRICS
dc.relation.ispartofTURKISH JOURNAL OF PEDIATRICS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectsolid pseudopapillary tumor
dc.subjectpediatric
dc.subjectpancreatic tumors
dc.subjectPEDIATRIC-PATIENTS
dc.subjectCHILDREN
dc.subjectNEOPLASMS
dc.titleSolid pseudopapillary tumor of the pancreas: a rare entity
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage312
oaire.citation.issue3
oaire.citation.startPage310
oaire.citation.titleTURKISH JOURNAL OF PEDIATRICS
oaire.citation.volume56

Files