The clinical variant of a T-cell lymphoma which may not be able to be distinguished pathologically.
The coding system used is (International Classification of Diseases for Oncology (ICD-O) Classification of Diseases for Oncology) Morphology coding, with an additional letter to make the code unique.
National Codes:
| M97003A | Mycosis fungoides |
| M97013A | Sezary syndrome |
| M97003B | Localised MF variants - pagetoid reticulosis (Woringer Kolopp disease) |
| M97003C | Other MF variants - follicular mucinosis |
| M97003D | Other MF variants - granulomatous slack skin |
| M97183A | CD30+ primary cutaneous lymphoproliferative disorders - lymphomatoid papulosis |
| M97183B | CD30+ primary cutaneous lymphoproliferative disorders - primary large cell anaplastic lymphoma |
| M97083A | Subcutaneous panniculitis-like T-cell lymphoma |
References:
National Cancer Dataset Version 2.1_ISB October 2002
This attribute is also known by these names:
| Context | Alias |
|---|---|
| plural | SKIN TCELL CLINICAL VARIANTS |