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Plasmablastic lymphoma: an atypical cutaneous presentation of a rare entity

dc.contributor.authorMota, F.
dc.contributor.authorMesquita, B.
dc.contributor.authorCarvalho, S.
dc.contributor.authorCoelho, A.
dc.contributor.authorVelho, G.
dc.contributor.authorLima, M.
dc.contributor.authorSelores, M.
dc.date.accessioned2017-06-13T11:12:45Z
dc.date.available2017-06-13T11:12:45Z
dc.date.issued2016-05-15
dc.description.abstractPlasmablastic lymphoma is a very rare B-cell lymphoma typically associated with immunosuppression: It occurs primarily in the oral cavity, although some cases were reported in other organs and tissues.To date, only 10 cases of primary cutaneous plasmablastic lymphoma have been described. Clinically, primary cutaneous plasmablastic lymphoma presents as non-specific cutaneous lesions (purple nodules, erythematous infiltrated plaques). In previously described cases, as in this case, histology and immunohistochemistry are required to make the diagnosis. Owing to the rarity of this entity, there is no established therapy, which makes its management an individualized, patient-based decision.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationDermatology Online Journal 22 (5): 6pt_PT
dc.identifier.issn1087-2108
dc.identifier.urihttp://hdl.handle.net/10400.16/2109
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherUniversity of Californiapt_PT
dc.relation.publisherversionhttp://escholarship.org/uc/item/2x218828pt_PT
dc.subjectplasmablastic lymphomapt_PT
dc.subjectB-cell lymphomaspt_PT
dc.subjectHuman herpesvirus 8pt_PT
dc.subjectHIV infectionpt_PT
dc.titlePlasmablastic lymphoma: an atypical cutaneous presentation of a rare entitypt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceUnited States of Americapt_PT
oaire.citation.issue5pt_PT
oaire.citation.startPage6pt_PT
oaire.citation.titleDermatology online journalpt_PT
oaire.citation.volume22pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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