Table 8.

Immunophenotypic and genetic features of common T-cell neoplasms.

NeoplasmCD3 (S;C)CD5CD7CD4CD8CD30TCRNK16, 56Cytotoxic granuleEBVGenetic AbnormalityT-Receptor Genes
Abbreviations: R, rearranged; M, mutated; NK, natural killer cell; U, unmutated; O, ongoing mutations; TCR, T-cell receptor gene; Ig, immunoglobulin; NA, not available 
Key: + = >90% positive; +/− = > 50% positive; −/+ = < 50% positive; − = < 10% positive; Cytotoxic granule = TIA-1, perforin, and/or granzyme 
* Mutations in the Ig gene V region indicate exposure to antigen. 
T-prolymphocytic leukemia − +,+ +/− −/+ − αβ − − − inv 14 + 8 
T-large granular lymphoproliferative disease − +,+ − − αβ +,− − none known 
NK large granlular lymphoproliferative disease − − +, − − +/− − − −,+ none known 
Extranodal NK/T-cell lymphoma −;+ − −/+ − − − − NA,+ ++ none known 
Hepatosplenic T-cell lymphoma − − − − γδ>>αβ +,−/+ − i(7q)(q10) 
Enteropathy-type T-cell lymphoma − +/− +/− αβ>>γδ − − none known 
Mycosis fungoides −/+ − − αβ − − − None known 
Cutaneous anaplastic large cell lymphoma +/− +/− +/− − ++ αβ − −/+ − none known 
Subcutaneous panniculitis-like T-cell − −/+ αβ>γδ −,+/− − none known 
Peripheral T-cell lymphoma, unspecified +/− +/− +/− +/− −/+ −/+ αβ>γδ −/+ −/+ −/+ inv 14; +8, complex 
Angioimmunoblastic +/− −/+ − αβ − NA +/− +3 +5 +X 
Primary systemic anaplastic large cell lymphoma +/− +/− NA −/+ −/+ ++ αβ − − t(2;5); NPM/ALK 
NeoplasmCD3 (S;C)CD5CD7CD4CD8CD30TCRNK16, 56Cytotoxic granuleEBVGenetic AbnormalityT-Receptor Genes
Abbreviations: R, rearranged; M, mutated; NK, natural killer cell; U, unmutated; O, ongoing mutations; TCR, T-cell receptor gene; Ig, immunoglobulin; NA, not available 
Key: + = >90% positive; +/− = > 50% positive; −/+ = < 50% positive; − = < 10% positive; Cytotoxic granule = TIA-1, perforin, and/or granzyme 
* Mutations in the Ig gene V region indicate exposure to antigen. 
T-prolymphocytic leukemia − +,+ +/− −/+ − αβ − − − inv 14 + 8 
T-large granular lymphoproliferative disease − +,+ − − αβ +,− − none known 
NK large granlular lymphoproliferative disease − − +, − − +/− − − −,+ none known 
Extranodal NK/T-cell lymphoma −;+ − −/+ − − − − NA,+ ++ none known 
Hepatosplenic T-cell lymphoma − − − − γδ>>αβ +,−/+ − i(7q)(q10) 
Enteropathy-type T-cell lymphoma − +/− +/− αβ>>γδ − − none known 
Mycosis fungoides −/+ − − αβ − − − None known 
Cutaneous anaplastic large cell lymphoma +/− +/− +/− − ++ αβ − −/+ − none known 
Subcutaneous panniculitis-like T-cell − −/+ αβ>γδ −,+/− − none known 
Peripheral T-cell lymphoma, unspecified +/− +/− +/− +/− −/+ −/+ αβ>γδ −/+ −/+ −/+ inv 14; +8, complex 
Angioimmunoblastic +/− −/+ − αβ − NA +/− +3 +5 +X 
Primary systemic anaplastic large cell lymphoma +/− +/− NA −/+ −/+ ++ αβ − − t(2;5); NPM/ALK 
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