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Primary gastric plasmacytoma: a rare entity

dc.contributor.authorOliveira, RC
dc.contributor.authorAmaro, P
dc.contributor.authorJulião, MJ
dc.contributor.authorCipriano, MA
dc.date.accessioned2017-09-01T10:33:35Z
dc.date.available2017-09-01T10:33:35Z
dc.date.issued2017-02-06
dc.description.abstractExtramedullary plasmacytomas (EP) are tumours composed by a monoclonal population of plasma cells that arise in extraosseus tissues, comprising <5% of all plasma cell neoplasms. Usually, EP arise in the head and neck region, and the stomach is the second most common location-gastric plasmacytoma (GP). Clinical and radiological manifestations are unspecific and may mimic other tumours like gastric adenocarcinomas, gastric stromal tumours and lymphomas, mainly marginal cell lymphoma (MALT lymphoma) and usually definitive diagnosis is provided by pathological evaluation. We present a case of primary GP, discovered incidentally as a polypoid lesion. Tumour was composed by sheets of mature and immature plasmocytes positive for CD138 on immunohistochemistry, without Helicobacter pylori identification. The patient is alive 6 years later and without tumour relapse.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationBMJ Case Rep. 2017 Feb 6;2017. pii: bcr2016218967.pt_PT
dc.identifier.doi10.1136/bcr-2016-218967pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.4/2089
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectLinfoma de Zona Marginal Tipo Células Bpt_PT
dc.subjectNeoplasias do Estômagopt_PT
dc.subjectPlasmocitomapt_PT
dc.titlePrimary gastric plasmacytoma: a rare entitypt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.startPagebcr2016218967pt_PT
oaire.citation.volume2017pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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