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Solitary bone plasmacytoma of the pelvis: a rare tumor

dc.contributor.authorKarmali, S
dc.contributor.authorBarros, A
dc.contributor.authorRosa, B
dc.contributor.authorCampos, P
dc.contributor.authorGonçalves, R
dc.contributor.authorSá da Costa, D
dc.contributor.authorLópez-Presa, D
dc.date.accessioned2016-04-11T21:06:54Z
dc.date.available2016-04-11T21:06:54Z
dc.date.issued2016
dc.description.abstractSolitary bone plasmacytomas are part of a wide range of monoclonal neoplasms that share a common progenitor in the B lymphocyte lineage. In their particular case, a single bone lesion is found, most frequently on the axial skeleton, having evidence of no other osteolytic lesions or systemic involvement. Diagnosis can sometimes prove to be difficult as they are rare tumors, occurring in 3 to 5% (up to 10% in some series) of patients with plasma cell neoplasms, with important considerations regarding the differential diagnosis. We report a case of a solitary bone plasmacytoma, found on the ala of the left ilium of a patient during a routine consult due to hip pain.pt_PT
dc.identifier.citationRare Tumors. 2016; 3:6306pt_PT
dc.identifier.doi10.4081/rt.2016.6306
dc.identifier.doi10.4081/rt.2016.6306
dc.identifier.urihttp://hdl.handle.net/10400.26/13102
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectPlasmacitomapt_PT
dc.subjectNeoplasias dos Ossospt_PT
dc.titleSolitary bone plasmacytoma of the pelvis: a rare tumorpt_PT
dc.typejournal article
dspace.entity.typePublication
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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