Онкогематология (Feb 2018)

REACTIVE PLASMACYTOSIS AT THE ONSET OF ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA. CASE REPORT

  • N. G. Chernova,
  • M. N. Sinitsyna,
  • A. M. Kovrigina,
  • Y. V. Sidorova,
  • I. V. Galtseva,
  • S. A. Mar’ina,
  • V. N. Dvirnyk,
  • E. E. Zvonkov

DOI
https://doi.org/10.17650/1818-8346-2017-12-4-28-33
Journal volume & issue
Vol. 12, no. 4
pp. 28 – 33

Abstract

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Angioimmunoblastic T-cell lymphoma is a rare T-cell lymphoproliferative disease with generalized lymphadenopathy, hepatosplenomegaly, intoxication and polyclonal hypergammaglobulinemia. The persistence of plasma cells in peripheral blood can be a manifestation of both tumor and reactive processes. In our article, we described the case of angioimmunoblastic T-cell lymphoma with an increase in the number of peripheral blood plasma cells to 28 %, and in bone marrow to 9 %. The complex diagnostics, including plasma cells immunophenotyping, morphology of the lymph node biopsy and bone marrow samples, made it possible to verify the diagnosis of angioimmunoblastic T-cell lymphoma with polyclonal plasmacytosis.

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