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Pancreas Burkitt primary lymphoma in pediatric age

dc.contributor.authorAraújo, J.
dc.contributor.authorSampaio-Macedo, C.
dc.contributor.authorSousa, L.
dc.date.accessioned2017-09-04T16:33:09Z
dc.date.available2017-09-04T16:33:09Z
dc.date.issued2017-06
dc.description.abstractWe present an the case of an eight-year-old Portuguese boy with no history of traveling, admitted with non-specific abdominal pain. An analytic study revealed high levels of lipase and amylase. Ultrasound, abdominal computerized tomography (CT), and an abdominal magnetic resonance imaging (MRI), were performed. The imaging findings are suggestive of a pancreatic tumor which is an extremely rare entity in children. A biopsy was performed by opened surgery and identified a Burkitt lymphoma.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationRev Esp Enferm Dig. 2017 Jun;109(6):451pt_PT
dc.identifier.issn1130-0108
dc.identifier.urihttp://hdl.handle.net/10400.16/2177
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherAran Edicionespt_PT
dc.relation.publisherversionhttps://www.reed.es/ArticuloFicha.aspx?id=1725&hst=0&idR=49&tp=1&AspxAutoDetectCookieSupport=1pt_PT
dc.titlePancreas Burkitt primary lymphoma in pediatric agept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceSpainpt_PT
oaire.citation.issue6pt_PT
oaire.citation.startPage451pt_PT
oaire.citation.titleRevista española de enfermedades digestivaspt_PT
oaire.citation.volume109pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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