[Plasmablastic lymphoma]

Med Clin (Barc). 2016 Nov 4;147(9):399-404. doi: 10.1016/j.medcli.2016.06.036. Epub 2016 Aug 28.
[Article in Spanish]

Abstract

Plasmablastic lymphoma (PBL) is a rare and aggressive subtype of non-Hodgkin lymphoma that commonly occurs in human immunodeficiency virus (HIV)-positive individuals, and affects oral sites. Occasionally, it has been described in HIV-negative patients and involving non-oral sites. Pathologically, PBL is a high-grade B-cell lymphoma that displays the immunophenotype of a terminally differentiated B-lymphocyte with loss of B-cell markers (CD20) and expression of plasma-cell antigens. Epstein-Barr virus infection and MYC rearrangements are frequently observed. Treatment of PBL is challenging because of the lack of established treatment and poor outcomes, with median survival times shorter than one year. In this review, we discuss the clinical and epidemiologic spectrum of PBL as well as its distinct pathological features. Finally, we summarize the currently available approaches for the treatment of patients with PBL.

Keywords: Bortezomib; Chemotherapy; Human immunodeficiency virus infection; Infección por el virus de la inmunodeficiencia humana; Linfoma plasmablástico; MYC; Oncogén MYC; Plasmablastic lymphoma; Quimioterapia.

Publication types

  • Review

MeSH terms

  • Diagnosis, Differential
  • Humans
  • Plasmablastic Lymphoma* / diagnosis
  • Plasmablastic Lymphoma* / epidemiology
  • Plasmablastic Lymphoma* / pathology
  • Plasmablastic Lymphoma* / therapy
  • Prognosis
  • Spain / epidemiology