Case report: 'Atypical Richter transformation from CLL-type monoclonal B-cell lymphocytosis into Burkitt lymphoma in a treatment naïve patient'.

Burkitt lymphoma MBL Richter transformation SLL/CLL state sequencing

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2024
Historique:
received: 18 09 2023
accepted: 09 04 2024
medline: 20 5 2024
pubmed: 20 5 2024
entrez: 20 5 2024
Statut: epublish

Résumé

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. 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 ( 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.

Sections du résumé

Background UNASSIGNED
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 UNASSIGNED
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 (
Conclusion UNASSIGNED
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.

Identifiants

pubmed: 38764580
doi: 10.3389/fonc.2024.1296238
pmc: PMC11099200
doi:

Types de publication

Case Reports

Langues

eng

Pagination

1296238

Informations de copyright

Copyright © 2024 Jauch, Alborelli, Reusser, Baschong, Rütsche, Bignucolo, Passweg, Dirnhofer and Krasniqi.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Annaïse J Jauch (AJ)

Division of Medical Oncology, University Hospital of Basel, Basel, Switzerland.

Ilaria Alborelli (I)

Institute of Medical Genetics & Pathology, Pathology, University Hospital Basel, Basel, Switzerland.

Andreas Reusser (A)

Division of Medical Oncology, Kantonsspital Basel-Land, Liestal, Switzerland.

Albert Baschong (A)

Institute for Pathology, Kantonsspital Basel-Land, Liestal, Switzerland.

Cyrill Rütsche (C)

Division of Hematology, University Hospital Basel, Basel, Switzerland.

Olivier Bignucolo (O)

Swiss Institute of Bioinformatics (SIB), Department of Biomedical Sciences, University of Lausanne, Basel, Switzerland.

Jakob Passweg (J)

Division of Hematology, University Hospital Basel, Basel, Switzerland.

Stefan Dirnhofer (S)

Institute of Medical Genetics & Pathology, Pathology, University Hospital Basel, Basel, Switzerland.

Fatime Krasniqi (F)

Division of Medical Oncology, University Hospital of Basel, Basel, Switzerland.

Classifications MeSH