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Peripheral T-cell and natural killer (NK)-cell lymphomas (PTCLs) represent a heterogeneous group of neoplasms derived from post-thymic T or NK cells, with diverse morphological patterns, phenotypes and clinical presentations. The International Consensus Classification and World Health Organization (WHO) classification of lymphoid and haematopoietic neoplasms recognise >30 PTCL entities1,2 (see Supplementary Table S1 and Supplementary Material Section 1, available at https://doi.org/10.1016/j.annonc.2025.01.023).
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d’Amore et al. (2025) studied this question.
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