G. Tallini et al., DIAGNOSIS OF GASTROINTESTINAL T-CELL LYMPHOMAS IN ROUTINELY PROCESSEDTISSUES, Journal of clinical gastroenterology, 17(1), 1993, pp. 57-66
Diagnosis of primary gastrointestinal T-cell lymphomas is often proble
matic because lymphoma may not be suspected clinically or on resection
, and tissue may not be frozen for immunophenotyping. Furthermore, ulc
eration and inflammation and the polymorphous character of the lesions
makes evaluation difficult. Only approximately 150 cases have been re
ported, fewer than 20 from North America. We have tried to establish a
reliable approach to the diagnosis of gastrointestinal lymphomas of T
-cell phenotype in routinely processed tissue. Sections from five prim
ary gastrointestinal T-cell lymphomas were stained with a panel of 13
antibodies reactive in routinely fixed, paraffin-embedded tissue. Thes
e included antibodies to pan-T- and pan-B-cell antigens (CD3, CD20), B
- and T-cell-associated antigens (CD43, CD45R0; CDw75, CD74), antigens
expressed by activated T-cells (HLA-DR, CD30), leukocyte antigens (CD
45, CD15), and macrophage markers (MAC-387, HAM-56). All stained posit
ively with T-cell markers MT-1 and Leu-22, four with UCHL-1, and three
with anti-CD3 polyclonal antibody. B-cell markers identified by L-26
and LN-1 were negative in all five, whereas LN-2 was expressed in two.
Two expressed HLA-DR; all were Ber-H2 negative. Two had an abnormal p
henotype: one was Leu-M1 positive, and one LCA negative. Ten B-cell ga
strointestinal lymphoma controls were negative for MT-1, Leu-22, and C
D3, and nine were negative for UCHL-1. Nine were positive for the B-ce
ll marker L-26, eight for LN-2, and seven for LN-1. All tumors were ne
gative for monocyte-macrophage markers. This antibody panel provides a
reliable means for identifying gastrointestinal T-cell lymphomas in p
araffin sections. Use of a panel is advisable because of variation in
expression and preservation of antigens, and to detect abnormal phenot
ypes. Application of this approach may facilitate the diagnosis of gas
trointestinal T-cell lymphomas both prospectively and in archival mate
rial, and thereby encourage studies of the behavior and treatment of t
hese neoplasms.