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. 2006 Jun 14;60(6):656–660. doi: 10.1136/jcp.2005.034199

Table 2 Summary of immunohistochemical and Epstein–Barr virus RNA in‐situ hybridisation results in nasal natural killer/T‐cell lymphomas.

Case CD3 CD4 CD8 CD79a CD56 CD57 CD3e TIA‐1 EBER (%)* Type F/“f” I/“i” XhoI
1 ++ +/− ++ −† ++ ++ 80 1 F “i” Loss
2 ++‡ −† ++ ++ ++ 90< 1 F NA Wild type
3 −† −§ −† ++ −§ ++ 90< 1 F NA Loss
4 ++‡ −† −† −† ++ −§ ++ ++ 80 NA “f” NA NA
5 ++ −§ ++ −† −† + ++ 70 1 F “i” Loss
6 ++‡ −† ++ −§ ++ ++ 0 NT NT NT NT
7 −§ −§ −† ++ NT ++ ++ 0 NT NT NT NT
8 −§ + + NT ++ ++ 90< 1 F “i” Loss
9 +‡ ++ −† NT ++ ++ 70 1 F “i” Wild type

EBER, Epstein–Barr virus‐encoded small RNA; NA, not amplified; NT, not tested.

*In‐situ hybridisation results were expressed as number of positive cells per medium‐powered field (×200). Cases were considered positive when a positive signal was observed in ⩾10% of the tumour cells.

†Background was also reacted.

‡Cytoplasmic expression was observed.

§Positive for reactive cells but not for neoplastic cells.