Table 2.
Pediatric T-cell lymphomas and relative frequency
| Common |
| T-lymphoblastic lymphoma |
| Anaplastic large-cell lymphoma, ALK positive |
| Less common and rare |
| Subcutaneous panniculitis-like T-cell lymphoma |
| Hepatosplenic T-cell lymphoma |
| Mycosis fungoides |
| Primary cutaneous CD30 + lymphoproliferative disorders |
| Lymphomatoid papulosis |
| Primary cutaneous anaplastic large-cell lymphoma |
| Peripheral T-cell lymphoma, NOS |
| Anaplastic large-cell lymphoma, ALK negative |
| Extranodal NK/T-cell lymphoma |
| Primary cutaneous gamma-delta T-cell lymphoma |
| Very rare |
| EBV-positive lymphoproliferations of childhood |
| Severe mosquito bite allergy |
| Systemic chronic active EBV disease, systemic |
| Systemic EBV + T-cell lymphoma of childhood |
| Hydroa vacciniforme lymphoproliferative disorder |
| Aggressive NK-cell leukemia |
| Primary cutaneous CD4 + small/medium T-cell LPD |
| T-cell large granular lymphocytic leukemia |
| Enteropathy-associated T-cell lymphoma |
| Adult T-cell leukemia/lymphoma |
Modified from [9, 13], underlined lymphoma are definitive subtypes in WHO Paediatric WHO Haematolymphoid disorders
LPD lymphoproliferative disorder, EBV Epstein-Barr virus, NOS not otherwise specified, NK natural killer cell, ALK anaplastic lymphoma kinase
Common, less common and rare, and very rare are terminology used by COG [9] but not defined. Common is rougly > 10% while very rare is < 1–2%