Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/29622
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorCORRIAS, Giuseppe-
dc.contributor.authorMONTI, Serena-
dc.contributor.authorHORVAT, Natally-
dc.contributor.authorTANG, Laura-
dc.contributor.authorBASTURK, Olca-
dc.contributor.authorSABA, Luca-
dc.contributor.authorMANNELLI, Lorenzo-
dc.date.accessioned2018-11-21T17:09:06Z-
dc.date.available2018-11-21T17:09:06Z-
dc.date.issued2018-
dc.identifier.citationCLINICAL IMAGING, v.51, p.59-64, 2018-
dc.identifier.issn0899-7071-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/29622-
dc.description.abstractBackground: Gastroenteropancreatic neuroendocrine tumors (NETs) are rare entities arising from neuroendocrine cells in the gastroenteric tract and pancreas. The purpose of this article is to present four cases of gastroenteropancreatic NETs that featured a challenging diagnosis. Case presentation: We report a case series of four NETs, each with different features. All NETs were suspected based on clinical and biochemical data. The workup of the abnormalities was performed with CT, PET or MRI. Conclusion: The diagnosis of NETs is challenging and generally based on clinical manifestations, blood biochemical tests, imaging techniques, and pathology.-
dc.description.sponsorshipMemorial Sloan-Kettering Cancer Center Support Grant/Core Grant [P30 CA008748]-
dc.description.sponsorshipISSNAF Imaging Science Chapter-
dc.description.sponsorshipEuropean Union's GlobusDoc Program-
dc.language.isoeng-
dc.publisherELSEVIER SCIENCE INC-
dc.relation.ispartofClinical Imaging-
dc.rightsrestrictedAccess-
dc.subjectNeuroendocrine tumors-
dc.subjectMRI-
dc.subjectOctreoscan-
dc.subjectInsulinoma-
dc.subjectGlucagonoma-
dc.subjectBiliary neuroendocrine tumor-
dc.subject.othersomatostatin receptor scintigraphy-
dc.subject.otherpancreatic tumors-
dc.subject.othercarcinoid-tumors-
dc.subject.otherendocrine tumors-
dc.subject.otherchromogranin-a-
dc.subject.othermanagement-
dc.subject.otherguidelines-
dc.subject.otherdiagnosis-
dc.subject.otherdisease-
dc.subject.otherpet-
dc.titleImaging features of malignant abdominal neuroendocrine tumors with rare presentation-
dc.typearticle-
dc.rights.holderCopyright ELSEVIER SCIENCE INC-
dc.identifier.doi10.1016/j.clinimag.2018.02.004-
dc.identifier.pmid29448120
dc.subject.wosRadiology, Nuclear Medicine & Medical Imaging-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.author.externalCORRIAS, Giuseppe:Mem Sloan Kettering Canc Ctr, Dept Radiol, 1275 York Ave, New York, NY 10065 USA; Univ Cagliari, Dept Radiol, Via Univ 40, I-09124 Cagliari, Italy-
hcfmusp.author.externalMONTI, Serena:IRCCS, SDN, Naples, Italy-
hcfmusp.author.externalTANG, Laura:Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10065 USA-
hcfmusp.author.externalBASTURK, Olca:Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10065 USA-
hcfmusp.author.externalSABA, Luca:Univ Cagliari, Dept Radiol, Via Univ 40, I-09124 Cagliari, Italy-
hcfmusp.author.externalMANNELLI, Lorenzo:Mem Sloan Kettering Canc Ctr, Dept Radiol, 1275 York Ave, New York, NY 10065 USA-
hcfmusp.description.beginpage59-
hcfmusp.description.endpage64-
hcfmusp.description.volume51-
hcfmusp.origemWOS-
hcfmusp.origem.idWOS:000445321000010-
hcfmusp.origem.id2-s2.0-85041849805-
hcfmusp.publisher.cityNEW YORK-
hcfmusp.publisher.countryUSA-
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dc.description.indexMEDLINE-
dc.identifier.eissn1873-4499-
hcfmusp.citation.scopus6-
hcfmusp.scopus.lastupdate2024-03-29-
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Instituto do Câncer do Estado de São Paulo - HC/ICESP

Artigos e Materiais de Revistas Científicas - ODS/03
ODS/03 - Saúde e bem-estar


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