Hematology Reports (Feb 2019)

Silent T-cell receptor cutaneous T-cell lymphoma associated to a clonal plasma cell proliferation

  • Ana Caballero,
  • Silvana Novelli,
  • Anna Mozos,
  • Pilar Garcia Muret,
  • Anna Monter,
  • Jorge Sierra,
  • Javier Briones

DOI
https://doi.org/10.4081/hr.2019.7841
Journal volume & issue
Vol. 11, no. 1

Abstract

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Within T-cell lymphomas (TCL) there are 2 entities expressing gamma-delta TCR: hepatosplenic gamma-delta T-cell lymphoma (HSGDTL) and the primary cutaneous gamma-delta T-cell lymphoma (PCGDTL). PCGDTL is a rare form of Tcell lymphoma with specific tropism for skin that have a dismal prognosis. Although even rarer, there have been reports of TCL with loss of expression of the TCR, which have been termed peripheral TCL TCR-silent type. We report the case of a cutaneous TCR-silent type lymphoma associated to a clonal plasma cell proliferation with an ominous outcome that led to a lot of discussion in its classification. Due to the aggressiveness of the disease and the scant evidence about therapy in this strange entity the outcome was fatal. We report a unique case of a TCR-silent cutaneous TCL with an exceptional histopathology, prolonged clinical evolution and a subsequent plasma cell clonal expansion.

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