Transformations of marginal zone lymphomas and lymphoplasmacytic lymphomas: Report from the 2021 SH/EAHP Workshop

Author:

Cook James R1ORCID,Amador Catalina2,Czader Magdalena3,Duffield Amy4,Goodlad John5,Ott German6,Xiao Wenbin4ORCID,Dave Sandeep7,Thakkar Devang7,Thacker Elizabeth8,Dogan Ahmet4,Wasik Mariusz9ORCID,Nejati Reza9

Affiliation:

1. Department of Laboratory Medicine, Robert J. Tomisch Pathology and Laboratory Medicine Institute, Cleveland Clinic , Cleveland, OH , US

2. Department of Pathology and Laboratory Medicine, University of Miami Miller School of Medicine , Miami, FL , US

3. Department of Pathology and Laboratory Medicine, Indiana University School of Medicine , Indianapolis, IN , US

4. Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Medical Center , New York, NY , US

5. Department of Pathology, NHS Greater Glasgow and Clyde , Glasgow , UK

6. Department of Clinical Pathology, Robert-Borsch-Krankenhaus, and Dr. Margarete Fischer-Bosch Institute for Clinical Pharmacology , Stuttgart , Germany

7. Duke University School of Medicine , Durham, NC , US

8. Data Driven Bioscience , Durham, NC , US

9. Department of Pathology, Fox Chase Cancer Center , Philadelphia, PA , US

Abstract

Abstract Objectives To summarize the conclusions of the 2021 Society for Hematopathology/European Association for Haematopathology workshop regarding transformations of marginal zone lymphoma (MZL) and lymphoplasmacytic lymphoma (LPL). Methods Nineteen cases were submitted to this portion of the workshop. Additional studies were performed in cases with sufficient material. Results Cases included splenic MZL (n = 4), splenic diffuse red pulp small B-cell lymphoma (n = 2), nodal MZL (n = 4), extranodal MZL (n = 1), and LPL (n = 8). The most common transformation was to diffuse large B-cell lymphoma (DLBCL), but others included classic Hodgkin lymphoma, high-grade B-cell lymphomas with MYC and BCL6 rearrangements, plasmablastic lymphoma, and plasma cell leukemia. Two splenic MZLs with transformation to DLBCL contained t(14;19)(q32;q13.3) IGH::BCL3 rearrangements in both samples. Paired sequencing studies in 5 MZLs with transformation to clonally related DLBCL identified a variety of mutations and gene fusions at the time of transformation, including CARD11, IGH::MYC, NOTCH2, P2RY8, TBLX1X1, and IGH::CD274. Conclusions Marginal zone lymphoma and LPL may undergo a variety of transformation events, most commonly to DLBCL, which is usually, although not always, directly clonally related to the underlying low-grade lymphoma. Multiparameter analysis including broad-based sequencing studies can assist in the diagnosis and classification of these uncommon cases.

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Reference36 articles.

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4. MYD88 L265P mutation analysis helps define nodal lymphoplasmacytic lymphoma;Hamadeh;Mod Pathol.,2015

5. Lymphoplasmacytic lymphoma and marginal zone lymphoma;Juárez-Salcedo;Hematol Oncol Clin North Am.,2019

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