dc.contributorUniversidade Federal de São Paulo (UNIFESP)
dc.creatorSchettini, Sergio Tomaz [UNIFESP]
dc.creatorRibeiro, R. C. [UNIFESP]
dc.creatorFacchin, C. G. [UNIFESP]
dc.creatorAbib, Simone de Campos Vieira [UNIFESP]
dc.date.accessioned2016-01-24T13:52:15Z
dc.date.accessioned2022-10-07T21:41:10Z
dc.date.available2016-01-24T13:52:15Z
dc.date.available2022-10-07T21:41:10Z
dc.date.created2016-01-24T13:52:15Z
dc.date.issued2009-02-01
dc.identifierEuropean Journal of Pediatric Surgery. Stuttgart: Georg Thieme Verlag Kg, v. 19, n. 1, p. 38-40, 2009.
dc.identifier0939-7248
dc.identifierhttp://repositorio.unifesp.br/handle/11600/31303
dc.identifier10.1055/s-2008-1038628
dc.identifierWOS:000264062000009
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/4031251
dc.description.abstractWe report a case of gastrinoma in a child and review the literature on gastrinoma in childhood, particularly with regard to the clinical, laboratory, radiological and scintigraphic characteristics, therapeutic approaches and prognosis. An eleven-year-old boy with gastrinoma underwent surgical resection. One year later resection of the left lateral lobe of the liver was performed due to a liver metastasis. the boy has been followed up for four years since this last procedure. the outcome was satisfactory for one year after the primary resection and then for a further four years after resection of a liver metastasis. Based on our data and that of the literature, it is our opinion that gastrinoma should be considered as a potentially malignant disease. the best approach is an early diagnosis and surgical treatment through resection of the primary tumor, followed by periodic postoperative clinical, laboratory, radiological and scintigraphic evaluations, because of the risk of metastatic disease. Such metastases must be resected as soon as possible.
dc.languageeng
dc.publisherGeorg Thieme Verlag Kg
dc.relationEuropean Journal of Pediatric Surgery
dc.rightsAcesso restrito
dc.subjectgastrinoma
dc.subjectneuroendocrine tumors
dc.subjectZollinger-Ellison syndrome
dc.subjectChildren
dc.titleGastrinoma in Childhood: Case Report and Update on Diagnosis and Treatment
dc.typeArtigo


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