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5.A 2017 World Health Organization Classification of Mature T- and NK-cell Neoplasms
T‐cell prolymphocytic leukemia
T‐cell large granular lymphocytic leukemia
Chronic lymphoproliferative disorder of natural killer cells
Aggressive natural killer (NK) cell leukemia
Systemic Epstein–Barr virus‐positive T‐cell lymphoma of childhood (a)
Hydroa vacciniforme‐like lymphoproliferative disorder
Adult T‐cell leukemia/lymphoma
Extranodal NK/T‐cell lymphoma, nasal type
Intestinal T‐cell lymphoma:
Enteropathy‐associated T‐cell lymphoma
Monomorphic epitheliotropic intestinal T‐cell lymphoma
Indolent T‐cell lymphoproliferative disorder of the gastrointestinal tract
Hepatosplenic T‐cell lymphoma
Subcutaneous panniculitis‐like T‐cell lymphoma
Mycosis fungoides
Sézary syndrome
Primary cutaneous CD30+ T‐cell lymphoproliferative disorders:
Lymphomatoid papulosis
Primary cutaneous anaplastic large‐cell lymphoma
Primary cutaneous peripheral T‐cell lymphomas, rare subtypes:
Primary cutaneous gamma–delta T‐cell lymphoma
Primary cutaneous CD8+ aggressive epidermotropic cytotoxic T‐cell lymphoma
Primary cutaneous acral CD8+ T‐cell lymphoma
Primary cutaneous CD4+ small/medium T‐cell lymphoproliferative disorder
Peripheral T‐cell lymphoma, not otherwise specified
Angioimmunoblastic T‐cell lymphoma and other nodal lymphomas of T‐follicular helper (Tfh) origin:
Angioimmunoblastic T‐cell lymphoma
Follicular T‐cell lymphoma
Nodal peripheral T‐cell lymphoma with Tfh phenotype
Anaplastic lymphoma kinase negative anaplastic large‐cell lymphoma
Anaplastic lymphoma kinase positive anaplastic large‐cell lymphoma
Breast implant‐associated anaplastic large‐cell lymphoma
Provisional entities are listed in italics.
Source: Swerdlow et al. [9].
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