Rare Tumors (Apr 2016)

Solitary bone plasmacytoma of the pelvis: a rare tumor

  • Samir Karmali,
  • André Barros,
  • Bárbara Rosa,
  • Pedro Campos,
  • Ricardo Gonçalves,
  • Daniel Sá da Costa,
  • Dolores López-Presa

DOI
https://doi.org/10.4081/rt.2016.6306
Journal volume & issue
Vol. 8, no. 1

Abstract

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Solitary 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.

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