Transdifferentiation, phenotypic infidelity, progression, and transformation in T/NK-cell neoplasms: Report from the 2021 SH/EAHP Workshop

Author:

Amador Catalina1,Cook James R2ORCID,Czader Magdalena3,Duffield Amy4,Goodlad John5,Nejati Reza6,Ott German7,Xiao Wenbin4ORCID,Dave Sandeep8,Wasik Mariusz A6ORCID,Dogan Ahmet4

Affiliation:

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

2. Department of Laboratory Medicine, Cleveland Clinic , Cleveland, OH , 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 Cancer Center , New York, NY , US

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

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

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

8. Department of Medicine, Duke University School of Medicine , Durham, NC , US

Abstract

AbstractObjectivesSessions 8 and 9 of the 2021 Society for Hematopathology and the European Association for Haematopathology Workshop aimed to collect examples of transdifferentiation, lineage infidelity, progression, and transformation in precursor and mature T/natural killer (NK)–cell neoplasms.MethodsTwenty-eight cases were submitted and analyzed, with whole-exome sequencing and genome-wide RNA expression analysis performed in a subset of the cases.ResultsIn session 8, 7 T-lymphoblastic lymphoma/leukemia cases were received that showed transdifferentiation to clonally related mature myeloid hematopoietic neoplasms, including 6 histiocytic/dendritic cell lineage neoplasms and a mast cell sarcoma. Session 9 included 21 mature T-cell neoplasms that were grouped into 3 themes. The first one addressed phenotypic infidelity in mature T-cell lymphomas (TCLs) and included 8 TCLs expressing aberrant antigens, mimicking classic Hodgkin and non-Hodgkin B-cell lymphomas. The second theme addressed disease progression in TCL and included 5 cutaneous T-cell lymphoproliferative disorders and 2 T-cell large granular lymphocyte proliferations with subsequent progression to systemic TCL. The third theme included 6 patients with TCL with T-follicular helper phenotype, mainly angioimmunoblastic T-cell lymphoma, with concurrent/subsequent clonal hematopoiesis or myeloid neoplasms and/or subsequent/concomitant diffuse large B-cell lymphoma.ConclusionsThis cohort of cases allowed us to illustrate, discuss, and review current concepts of transdifferentiation, aberrant antigen expression, and progression in various T/NK-cell neoplasms.

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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