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Solid pseudopapillary neoplasm-Case report of a rare pancreatic tumor

dc.contributor.authorBranco, C
dc.contributor.authorVilaça, S
dc.contributor.authorFalcão, J
dc.date.accessioned2017-03-31T12:39:25Z
dc.date.available2017-03-31T12:39:25Z
dc.date.issued2017-02-28
dc.description.abstractINTRODUCTION: Solid pseudopapillary neoplasm (SPN) is a rare pancreatic tumor. Most patients are female within the second or third decade of life with only a small minority concerning children. Frequently described as low malignant potential tumors, surgical resection remains the main treatment. PRESENTATION OF CASE: The authors present a case of a SPN diagnosed in a 17-year-old Caucasian girl with vomiting and abdominal pain localized to the right upper quadrant. CT scans and MRI scans showed the presence of a well-defined tumor arising from the pancreatic head with 14cm of greater diameter. Pylorus-preserving pancreatoduodenectomy was performed and histopathology confirmed a SPN with complete resection and no evidence of malignancy. DISCUSSION: SPN are usually found incidentally hence the importance of an accurate radiologic diagnosis. Symptoms may be present such as abdominal pain or vomiting due to compression, namely in large tumors. A surgical approach is usually indicated aiming complete resection, with tumor size not predicting resectability. CONCLUSION: Solid pseudopapillary tumors of the pancreas are extremely rare and usually have an excellent long-term prognosis after surgical resection.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationInt J Surg Case Rep. 2017 Feb 28;33:148-150.pt_PT
dc.identifier.doi10.1016/j.ijscr.2017.02.049pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.23/1165
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectNeoplasias do Pâncreaspt_PT
dc.titleSolid pseudopapillary neoplasm-Case report of a rare pancreatic tumorpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage150pt_PT
oaire.citation.startPage148-150pt_PT
oaire.citation.volume33pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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