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dc.contributor.authorDaroit, Natália Batistapt_BR
dc.contributor.authorSilva, Viviane Palmeira dapt_BR
dc.contributor.authorMaraschin, Bruna Jalfimpt_BR
dc.contributor.authorVisioli, Fernandapt_BR
dc.contributor.authorAleixo, Pedro Bandeirapt_BR
dc.contributor.authorOliveira, Márcia Gaiger dept_BR
dc.contributor.authorRados, Pantelis Varvakipt_BR
dc.date.accessioned2018-06-09T03:34:06Zpt_BR
dc.date.issued2017pt_BR
dc.identifier.issn2231-0614pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/179249pt_BR
dc.description.abstractPlasmablastic Lymphoma (PBL) is a hematolymphoid malignant disease that has a predilection for the oral cavity and jaw. The aim of this paper is report a total resolution of oral manifestation of PBL without any oncological treatment; this process is extremely rare and we discuss the mechanism which can occur. We present a case of PBL in left maxilla and oral mucosa in a woman HIV-positive patient. After an incisional biopsy an unusual outcome of spontaneous regression of the disease occurred, we reported the diagnostic process, the management and the follow up of case. We revised the similar cases reported in the literature and we will discuss the hypotheses how the phenomenon can occur. Although the PBLs are aggressive lesions, with questionable prognosis, the spontaneous regression can occur and the patient should be monitored for the risk of metastases and possible recurrence of the disease.en
dc.format.mimetypeapplication/pdf
dc.language.isoengpt_BR
dc.relation.ispartofBritish journal of medicine and medical research. Gurgaon, India. Vol. 21, no. 11 (2014), p. 1-7pt_BR
dc.rightsOpen Accessen
dc.subjectPatologia bucalpt_BR
dc.subjectAcquired immunodeficiency syndromeen
dc.subjectJaw canceren
dc.subjectMaxillaen
dc.subjectPlasmablastic lymphomaen
dc.subjectSpontaneous neoplasm regressionen
dc.titleSpontaneous regression of an oral manifestation of Plasmablastic Lymphoma : literature review and commentary about the phenomenapt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001068905pt_BR
dc.type.originEstrangeiropt_BR


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