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Indolent B-cell lymphoma with t(14;19) investigated from a molecular perspective

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Abstract

T(14;19) is an unusual but distinct genomic alteration reported in low-grade B-cell lymphomas. This structural rearrangement places BCL3 in juxtaposition with IGH inducing proliferation and has been found in chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), marginal zone lymphoma (MZL), and other low-grade B-cell lymphomas. While there are some case series describing this in the context of other cytogenetic alterations, there are limited clinical cases examined from a molecular perspective. We herein describe a case of a low-grade B-cell lymphoma with t(14;19) resulting in IGH::BCL3 fusion on which we performed whole exome sequencing to investigate genetic variants that could contribute to its pathogenesis. We found pathogenic alterations including a variant in CXCR4 which has been shown to be recurrently mutated in different low-grade B-cell lymphomas including lymphoplasmacytic lymphoma (LPL) and MZL. We describe this interesting case in the context of its genomic findings and how it contributes to the literature as a whole.

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References

  1. Michaux L et al (1996) BCL3 rearrangement and t(14;19)(q32;q13) in lymphoproliferative disorders. Genes Chromosomes Cancer 15(1):38–47

    Article  CAS  PubMed  Google Scholar 

  2. Yang H et al (2022) Clinical analysis of 20 cases of small B lymphocyte proliferative disease with t (14;19) (q32;q13). Zhonghua Xue Ye Xue Za Zhi 43(8):674–679

    CAS  PubMed  Google Scholar 

  3. Huh YO et al (2011) Chronic lymphocytic leukemia with t(14;19)(q32;q13) is characterized by atypical morphologic and immunophenotypic features and distinctive genetic features. Am J Clin Pathol 135(5):686–696

    Article  PubMed  Google Scholar 

  4. Schweighofer CD et al (2011) The B cell antigen receptor in atypical chronic lymphocytic leukemia with t(14;19)(q32;q13) demonstrates remarkable stereotypy. Int J Cancer 128(11):2759–2764

    Article  CAS  PubMed  Google Scholar 

  5. Huh YO et al (2007) The t(14;19)(q32;q13)-positive small B-cell leukaemia: a clinicopathologic and cytogenetic study of seven cases. Br J Haematol 136(2):220–228

    Article  CAS  PubMed  Google Scholar 

  6. Nguyen-Khac F et al (2006) The t(14;19)(q32;q13) Translocation in B lymphoproliferative disorders: a continuum from chronic lymphocytic leukemia (CLL) to marginal zone lymphoma (MZL)? Blood 108(11):4944

    Article  Google Scholar 

  7. Carbó-Meix A et al (2021) Whole genome sequencing of B-cell neoplasms with t(14;19)(q32;q13) reveals different entities. Blood 138(Supplement 1):3709–3709

    Article  Google Scholar 

  8. Michaux L et al (1997) t(14;19)/BCL3 rearrangements in lymphoproliferative disorders: a review of 23 cases. Cancer Genet Cytogenet 94(1):36–43

    Article  CAS  PubMed  Google Scholar 

  9. Alaggio R et al (2022) The 5th edition of the World Health Organization classification of haematolymphoid tumours: lymphoid neoplasms. Leukemia 36(7):1720–1748

    Article  PubMed  PubMed Central  Google Scholar 

  10. Campo E et al (2022) The international consensus classification of mature lymphoid neoplasms: a report from the clinical advisory committee. Blood 140(11):1229–1253

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Poulain S et al (2016) Genomic landscape of CXCR4 Mutations in Waldenström Macroglobulinemia. Clin Cancer Res 22(6):1480–1488

    Article  CAS  PubMed  Google Scholar 

  12. Cancilla D, Rettig M, DiPersio JF (2020) Targeting CXCR4 in AML and ALL. Front Oncol 10:1672

    Article  PubMed  PubMed Central  Google Scholar 

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Authors and Affiliations

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Jeremiah Karrs DO: primary author, case review; Shivaprasad H. Sathyanarayana PhD: contributing author; Xinjie Xu PhD: FISH image, editing; Donald C. Green BS: bioinformatics support for sequencing; Wahab A. Kahn PhD: cytogenetic analysis; Eric Y. Loo MD: editing; Prabhjot Kaur MD: senior author, case review.

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Correspondence to Jeremiah X. Karrs.

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Karrs, J.X., Sathyanarayana, S.H., Xu, X. et al. Indolent B-cell lymphoma with t(14;19) investigated from a molecular perspective. J Hematopathol 16, 217–221 (2023). https://doi.org/10.1007/s12308-023-00562-7

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  • DOI: https://doi.org/10.1007/s12308-023-00562-7

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