A Diagnostic Approach to the Identification of Burkitt-like Lymphoma With 11q Aberration in Aggressive B-Cell Lymphomas.


Journal

The American journal of surgical pathology
ISSN: 1532-0979
Titre abrégé: Am J Surg Pathol
Pays: United States
ID NLM: 7707904

Informations de publication

Date de publication:
01 03 2021
Historique:
pubmed: 3 11 2020
medline: 31 3 2021
entrez: 2 11 2020
Statut: ppublish

Résumé

Rare cases of aggressive B-cell lymphomas with a morphology similar to Burkitt lymphoma (BL) present with the BL-typical immunophenotype, but lacked MYC translocation (MYC-negative Burkitt-like lymphoma: mnBLL). A proportion of those with an imbalance pattern in chromosome 11q has been designated Burkitt-like lymphoma with 11q aberration in the recent update of the World Health Organization (WHO) classification. Because of the problems in the identification of Burkitt-like lymphoma with 11q aberration, our goal was to retrospectively analyze their frequency in a cohort of "candidate" aggressive lymphomas (cohort 1, n=35) such as mnBLL (n=16), diffuse large B-cell lymphoma with similarities to Burkitt lymphoma (DLBCL-BL; n=3), high-grade B-cell lymphomas, not otherwise specified (NOS) (n=16), as well as in a cohort of MYC-negative diffuse large B-cell lymphoma NOS (cohort 2, n=62). In total, 17/33 cohort 1 cases (52%) harbored the typical 11q aberration pattern, predominantly those that had been classified as mnBLL (12/16, 75%), but also as DLBCL-BL (2/3, 67%) and high-grade B-cell lymphomas, NOS (3/14; 21%). The specimens with this typical 11q aberration pattern were usually negative for the BCL2 protein. Of interest and as a new finding, samples harboring the 11q aberration pattern were often characterized by strikingly coarse apoptotic debris within starry sky macrophages facilitating their recognition. In contrast, only 1 of 62 garden variety DLBCL, NOS was positive for the 11q aberration pattern. In 2 DLBCL-BL, a dual MYC translocation/11q aberration pattern was detected. As a diagnostic algorithm, we, therefore, propose analysis of 11q status in MYC-negative high-grade lymphomas with features of BL, especially showing BCL2 negativity and a conspicuous coarse apoptotic debris in starry sky macrophages.

Identifiants

pubmed: 33136583
pii: 00000478-202103000-00007
doi: 10.1097/PAS.0000000000001613
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

356-364

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest and Source of Funding: Supported by the German José Carreras Leukämie-Stiftung (DJCLS R 10/28) and the Robert Bosch-Stiftung (Project O3), Stuttgart, Germany. The authors have disclosed that they have no significant relationships with, or financial interest in, any commercial companies pertaining to this article.

Références

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Auteurs

Heike Horn (H)

Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology.
Department of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart.
University of Tübingen, Tübingen.

Sabrina Kalmbach (S)

Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology.
University of Tübingen, Tübingen.

Rabea Wagener (R)

Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm.
Department of Pediatric Oncology, Hematology and Clinical Immunology, University Children's Hospital, Medical Faculty, Heinrich-Heine-University Düsseldorf, Düsseldorf.

Annette M Staiger (AM)

Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology.
Department of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart.
University of Tübingen, Tübingen.

Katrin Hüttl (K)

Department of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart.

Anja Mottok (A)

Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm.

Susanne Bens (S)

Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm.

Alexandra Traverse-Glehen (A)

Service d'Anatomie Pathologie, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.

Juliette Fontaine (J)

Service d'Anatomie Pathologie, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.

Reiner Siebert (R)

Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm.

Andreas Rosenwald (A)

Institute of Pathology, Universität Würzburg and Comprehensive Cancer Center Mainfranken (CCCMF), Würzburg, Germany.

German Ott (G)

Department of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart.

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