Table 1.
Mature T-Cell and NK-Cell Neoplasms |
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Nodal Peripheral T-cell lymphoma, NOS Angioimmunoblastic T-cell lymphoma Anaplastic large-cell lymphoma, ALK+ Anaplastic large-cell lymphoma, ALK− Follicular T-cell lymphoma Nodal peripheral T-cell lymphoma with TFH phenotype Systemic EBV+ T-cell lymphoma of childhood Hydroa vacciniforme-like lymphoproliferative disorder |
Extranodal Monomorphic epitheliotropic intestinal T-cell lymphoma Indolent T-cell lymphoproliferative disorder of the GI tract Breast implant-associated anaplastic large-cell lymphoma Enteropathy-associated T-cell lymphoma Extranodal NK-/T-cell lymphoma, nasal type Chronic lymphoproliferative disorder of NK cells Hepatosplenic T-cell lymphoma |
Cutaneous Sézary syndrome Mycosis fungoides Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder Primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma Primary cutaneous acral CD8+ T-cell lymphoma Subcutaneous panniculitis-like T-cell lymphoma Primary cutaneous CD30+ T-cell lymphoproliferative disorders
Lymphomatoid papulosis Primary cutaneous anaplastic large cell lymphoma |
Leukemic form Aggressive NK-cell leukemia T-cell large granular lymphocytic leukemia T-cell prolymphocytic leukemia Adult T-cell leukemia/lymphoma |
Note: Data based on the WHO 2016 classification data from Swerdlow et al.3
Abbreviations: GI, gastro-intestinal; NK, natural killer; NOS, not otherwise specified; ALK, anaplastic lymphoma kinase; TFH, T follicular helper; EBV, Epstein Barr virus.