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Case report: 'Atypical Richter transformation from CLL-type monoclonal B-cell lymphocytosis into Burkitt lymphoma in a treatment naïve patient'.
Jauch, Annaïse J; Alborelli, Ilaria; Reusser, Andreas; Baschong, Albert; Rütsche, Cyrill; Bignucolo, Olivier; Passweg, Jakob; Dirnhofer, Stefan; Krasniqi, Fatime.
Afiliação
  • Jauch AJ; Division of Medical Oncology, University Hospital of Basel, Basel, Switzerland.
  • Alborelli I; Institute of Medical Genetics & Pathology, Pathology, University Hospital Basel, Basel, Switzerland.
  • Reusser A; Division of Medical Oncology, Kantonsspital Basel-Land, Liestal, Switzerland.
  • Baschong A; Institute for Pathology, Kantonsspital Basel-Land, Liestal, Switzerland.
  • Rütsche C; Division of Hematology, University Hospital Basel, Basel, Switzerland.
  • Bignucolo O; Swiss Institute of Bioinformatics (SIB), Department of Biomedical Sciences, University of Lausanne, Basel, Switzerland.
  • Passweg J; Division of Hematology, University Hospital Basel, Basel, Switzerland.
  • Dirnhofer S; Institute of Medical Genetics & Pathology, Pathology, University Hospital Basel, Basel, Switzerland.
  • Krasniqi F; Division of Medical Oncology, University Hospital of Basel, Basel, Switzerland.
Front Oncol ; 14: 1296238, 2024.
Article em En | MEDLINE | ID: mdl-38764580
ABSTRACT

Background:

Richter transformation refers to the progression of an initially slow-growing small lymphocytic lymphoma/chronic lymphocytic leukemia (SLL/CLL) into an aggressive lymphoma, typically diffuse large B-cell lymphoma (DLBCL) or Hodgkin lymphoma. Case presentation The patient presented with a rapid onset of localized cervical swelling, accompanied by monoclonal B-cell lymphocytosis displaying a CLL immunophenotype. The histopathological analysis identified a Burkitt lymphoma (BL) located in the submandibular gland and adjacent lymph node. The patient's bone marrow displayed a minor infiltration of monoclonal B-cells with a CLL immunophenotype (< 10%). Molecular analysis demonstrated the presence of the same monoclonal rearrangement in the framework region (FR3 region) of the immunoglobulin heavy chain (IGH) locus. High-throughput sequencing of the immunoglobulin heavy and light chains also confirmed the presence of the same rearrangement in SLL/CLL and in the Burkitt lymphoma sample, but also highlighted the presence of a second rearrangement in the Burkitt lymphoma cells, not shared with the SLL/CLL cells in the bone marrow. The patient was treated with DA-EPOCH-R, which lead to a complete metabolic response.

Conclusion:

This report provides an exceptionally rare description of a CLL-type monoclonal B-cell lymphocytosis transforming into a very aggressive Burkitt lymphoma in a treatment naïve patient.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article