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. 2019 Jan 11;133(16):1703–1714. doi: 10.1182/blood-2018-11-881268

Table 3.

Characteristic clinical and immunophenotypic features of various types of CTCL

Clinical features T-cell phenotype Cytotoxic proteins CD56 Major lineage EBV
MF Patches and plaques; (ulcerating) tumors in advanced stage CD3+, CD4+, CD8 αβ T cell
C-ALCL Solitary or localized nodules or tumors CD3+/−, CD4+, CD8, CD30+ + αβ T cell
SPTCL Subcutaneous nodules and plaques CD3+, CD4, CD8+ + αβ T cell
PCGD-TCL Ulcerating plaques and tumors CD3+, CD4, CD8−/+ + + γδ T cell
Extranodal NK/T-cell lymphoma (Ulcerating) plaques and tumors CD3+, CD4, CD8+ (surface CD3) + + NK or γδ T cell +
CD8+ AECTCL Ulcerating plaques, nodules, and tumors CD3+, CD4, CD8+ + αβ T cell
Primary cutaneous acral CD8+ T-cell lymphoma Solitary papule or nodule on acral site (ear; nose) CD3+, CD4, CD8+ +/−* αβ T cell
Primary cutaneous CD4+ small/medium T-cell LPD Solitary nodule or tumor on the face or upper trunk CD3+, CD4+, CD8, CD279/PD-1+ αβ T cell

PCGD-TCL, primary cutaneous γ/δ T-cell lymphoma; SPTCL, subcutaneous panniculitis-like T-cell lymphoma.

*

Expresses a nonactivated cytotoxic phenotype, positive for TIA-1, but negative for other cytotoxic proteins.