Peripheral T-cell lymphomas: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
Line 20: | Line 20: | ||
**[[Primary cutaneous anaplastic large cell lymphoma]] | **[[Primary cutaneous anaplastic large cell lymphoma]] | ||
**[[Lymphomatoid papulosis]] | **[[Lymphomatoid papulosis]] | ||
* | *[[Primary cutaneous peripheral T-cell lymphomas]], rare subtypes | ||
**[[Primary cutaneous gamma-delta T-cell lymphoma]] | **[[Primary cutaneous gamma-delta T-cell lymphoma]] | ||
**[[Primary cutaneous CD8 positive aggressive epidermotropic cytotoxic T-cell lymphoma]] | **[[Primary cutaneous CD8 positive aggressive epidermotropic cytotoxic T-cell lymphoma]] |
Revision as of 18:12, 15 February 2015
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Alberto Plate [2]
The WHO classification of T-cells NHL categorize them into Precursor T-cell neoplasm and Peripheral T-cell lymphomas/NK-cell neoplasms. The last one can be further subdivided into:
- T-cell prolymphocytic leukemia
- T-cell large granular lymphocytic leukemia
- Chronic lymphoproliferative disorder of NK cells
- Aggressive NK-cell leukemia
- EBV positive T-cell lymphoproliferative disorders of childhood
- Systemic EBV positive T-cell lymphoproliferative disease of childhood
- Hydroa vacciniforme-like lymphoma
- Adult T-cell lymphoma/leukemia
- Extranodal T-/NK-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 disorders
- Primary cutaneous peripheral T-cell lymphomas, rare subtypes