K. Blakolmer et al., Immunoreactivity of B-cell markers (CD79a, L26) in rare cases of extranodal cytotoxic peripheral T- (NK/T-) cell lymphomas, MOD PATHOL, 13(7), 2000, pp. 766-772
Citations number
27
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
The monoclonal antibodies L26 (CD20) and CD79a are very useful reagents for
the immunohistochemical assessment of B-cell lineage in lymphoproliferativ
e disorders. Although very few CD20-positive peripheral T-cell lymphomas (P
TL) have been reported, comprehensive analyses of CD79a reactivity in extra
nodal PTL and NK/T-cell lymphomas have not been performed previously. This
study investigated CD79a (clone JCB117) and CD20 reactivity in 94 extranoda
l non-B-cell lymphomas (enteropathy-type intestinal T-cell. lymphoma [n = 5
2], nasal NK/T-cell lymphoma [n = 11], and primary cutaneous PTL [n = 31])
and in 17 cases of nodal PTL, unspecified. In four cases (enteropathy-type
intestinal T-cell lymphoma [n = 3] and nasal NK/T-cell lymphoma [n = 1)], t
he majority of tumor cells stained for CD79a (all CD20 negative) and one cu
taneous PTL, unspecified, was CD20 positive (CD79a negative). Extensive imm
unophenotyping and polymerase chain reaction-based molecular analyses revea
led that all five B-cell marker-positive extranodal lymphomas had a cytotox
ic phenotype and did indeed represent monoclonal peripheral T-cell prolifer
ations. To minimize the risk of misinterpretation of lymphoma cell lineage,
especially in cases of extranodal lymphoproliferative disease, we suggest
the use of both CD79a and CD20 in combination with a panel of antibodies re
active to T cells, such as beta F1 and CD5, and to T cells and NK cells, su
ch as CD3, CD2, CD56, and TIA-1.