Childhood and Adolescent Relapsed/Refractory Aggressive B-Cell Lymphomas With t(8;14) and BCL2 Expression, Burkitt Lymphoma Versus Diffuse Large B-Cell Lymphoma: A Diagnostic Challenge

Author:

El Dana Fouad1,Garces Narvaez Sofia Alexandra2,El-Mallawany Nader K.3,Agrusa Jennifer E.34,Dreyer ZoAnn E.3,Marcogliese Andrea N.13,Elghetany Mohamed Tarek13,Punia Jyotinder N.1,Ok Chi Young2,Patel Keyur P.2,Lopez-Terrada Dolores H.13,Fisher Kevin E.1ORCID,Curry Choladda V.1ORCID

Affiliation:

1. Department of Pathology & Immunology, Baylor College of Medicine and Texas Children’s Hospital, Houston, TX, USA

2. Department of Hematopathology, University of Texas MD Anderson Cancer Center, Houston, TX, USA

3. Department of Pediatrics, Section of Hematology-Oncology, Baylor College of Medicine and Texas Children’s Hospital, Houston, TX, USA

4. Division of Pediatric Hematology-Oncology, University of Michigan, Ann Arbor, MI, USA

Abstract

We present 2 diagnostically challenging cases of pediatric/adolescent relapsed/refractory aggressive mature B-cell non-Hodgkin lymphoma (B-NHL) within the spectrum of Burkitt lymphoma and diffuse large B-cell lymphoma and illustrate the different therapeutic regimens that are employed for pediatric and adult cancer centers. Both cases displayed varying-sized lymphoma cells with occasional single prominent nucleoli and heterogeneous BCL2 expression. Cytogenetics revealed complex karyotypes with t(8:14)(q24.2;q32) and IGH::MYC rearrangement by FISH. Next generation sequencing revealed deleterious TP53 and MYC mutations. We concluded that both could be diagnosed as “DLBCL-NOS with MYC rearrangement” using the current pathologic classifications, 2022 International Consensus Classification (ICC) and World Health Organization Classifications of Haematolymphoid Tumors (WHO-HAEM5). This report illustrates diagnostic challenges and treatment dilemmas that may be encountered, particularly for adolescent and young adults (AYA).

Publisher

SAGE Publications

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