Abstract

Peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS) is the most common entity of mature T-cell neoplasms. PTCL-NOS generally has an aggressive behavior and is often refractory to standard therapy. Only a few cases of PTCL with aberrant expression of B-cell antigens have been reported so far. This phenotypic aberrancy may lead to misdiagnosis as B-cell non-Hodgkin lymphomas and eventual inappropriate patient management, whereas in an accurately diagnosed PTCL, the presence of CD20 may appear as an appealing therapeutic target. In this setting, response to anti-CD20 monoclonal antibody in combination with chemotherapy has been poorly explored. We describe the case of a 59-year-old male diagnosed by a pathological and molecular approach as PTCL-NOS with aberrant co-expression of the B-cell antigens CD20 and CD79a, which proved non-responsive to the addition of rituximab to standard polychemotherapy. This case highlights that the presence of CD20 in PTCL may be misleading in the diagnosis and also act as a lure for the clinician to adopt a rituximab-based treatment, the effectiveness of which is undefined as the molecular mechanisms underlying B-cell marker expression in PTCL.

Highlights

  • The term peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS) encompasses a heterogeneous group of nodal and extranodal T-cell neoplasms derived from peripheral T lymphocytes exhibiting a broad cytological and phenotypic heterogeneity [1]

  • PTLC-NOS typically occur in adults and account for about 25% of all PTCL, which represent over 15% of all non-Hodgkin lymphomas in Europe and United States, being more common in Eastern countries [2]

  • We reported a PTCL-NOS with aberrant co-expression of CD20 and CD79a characterized by a very poor prognosis, and no benefit from the addition of rituximab to two different chemotherapy schedules

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Summary

Introduction

The term peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS) encompasses a heterogeneous group of nodal and extranodal T-cell neoplasms derived from peripheral T lymphocytes exhibiting a broad cytological and phenotypic heterogeneity [1]. PTCL-NOS frequently shows a defective T-cell phenotype with loss of CD5 and CD7 antigen expression and a prevalent CD4+/CD8phenotype in nodal cases. Only few cases of PTCL with aberrant expression of two or more B-cell antigens have been documented [14,15,16]. Some cases of primary T-cell lymphoma with co-expression of B-cell markers and clonal gene rearrangement for both TRG and IGH have been recently reported [17,18]. We describe a case of PTCL-NOS characterized by concomitant strong expression of CD20 and CD79a, in which treatment with rituximab plus dexamethasone, cisplatin and cytosine arabinoside (R-DHAP) and rituximab plus gemcitabine and oxaliplatin (R-GEMOX) were not effective

Molecular Findings
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