Table 1.
T-cell prolymphocytic leukemia |
T-cell large granular lymphocytic leukemia |
Chronic lymphoproliferative disorder of NK-cells* |
Aggressive NK cell leukemia |
Systemic EBV-positive T-cell lymphoproliferative disease of childhood (associated with chronic active EBV infection) |
Hydroa vacciniforme-like lymphoma |
Adult T-cell leukemia/lymphoma |
Extranodal NK/T-cell lymphoma, nasal type |
Enteropathy-associated T-cell lymphoma |
Hepatosplenic T-cell lymphoma |
Subcutaneous panniculitis-like T-cell lymphoma |
Mycosis fungoides |
Sézary syndrome |
Primary cutaneous CD30-positive T-cell lymphoproliferative disorder |
Lymphomatoid papulosis |
Primary cutaneous anaplastic large-cell lymphoma |
Primary cutaneous aggressive epidermotropic CD8-positive cytotoxic T-cell lymphoma* |
Primary cutaneous gamma-delta T-cell lymphoma |
Primary cutaneous small/medium CD4-positive T-cell lymphoma* |
Peripheral T-cell lymphoma, not otherwise specified |
Angioimmunoblastic T-cell lymphoma |
Anaplastic large cell lymphoma, ALK-positive |
Anaplastic large cell lymphoma, ALK-negative* |
ALK, anaplastic lymphoma kinase; EBV, Epstein Barr virus; NK, natural killer.
These represent provisional entities or provisional subtypes of other neoplasms.
Diseases shown in italics are newly included in the 2008 WHO classification.