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Abstract/Summary
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<jats:title>Abstract</jats:title><jats:p>Aggressive B-cell non-Hodgkin lymphomas are a heterogeneous group of diseases and our concepts are evolving as we learn more about their clinical, pathologic, molecular genetic features. Session IV of the 2020 EAHP Workshop covered aggressive, predominantly high-grade B-cell lymphomas, many that were difficult to classify. In this manuscript, we summarize the features of the submitted cases and highlight differential diagnostic difficulties. We specifically review issues related to high-grade B-cell lymphomas (HGBCLs) with <jats:italic>MYC</jats:italic> and <jats:italic>BCL2</jats:italic> and/or <jats:italic>BCL6</jats:italic> rearrangements including TdT expression in these cases, HGBCL, not otherwise specified, large B-cell lymphomas with <jats:italic>IRF4</jats:italic> rearrangement, high-grade/large B-cell lymphomas with 11q aberration, Burkitt lymphoma, and pleomorphic mantle cell lymphoma. Since the workshop, the 5th edition of the WHO Classification for Haematolymphoid Tumours (WHO-HAEM5) and International Consensus Classification (ICC) 2022 were published. We endeavor to use the updated terminology.</jats:p>
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Hinweis
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