Lymphoproliferative diseases are the most common disorders associated with
autoimmune disturbances. We determined the autoimmune phenotype of 64 non H
odgkin's lymphoma patients' and compared their clinicopathologic properties
. Serum direct antiglobulin rest [(DAT) n=64], indirect antiglobulin test [
(IAT) n=61], platelet autoantibodies [(PAA) n=51], anti nuclear antibodies
[n=33], anti-native DNA [n=29], anti phospholipid antibodies [n=40] and. lu
pus anticoagulant [n=33] were used as autoimmune markers, Twenty five patie
nts (39 %) displayed one or more autoimmune marker positivity (+). Three pa
tients with (+) DAT and IAT had autoimmune hemolytic anemia and two patient
s with PAA had autoimmune thrombocytopenia. Male patients were more suscept
ible to autoimmunity in low grade lymphomas and the statistical difference
was significant (p=0.035). Most of the autoimmune markers (+) patients had
low grade and disseminated disease but this was not significant, Remission
rates were not found to be different between autoimmune marker (+) and (-)
patients. Although statistically not significant, median survival was longe
r in autoimmune marker (-) patients than in the others (50 versus 39 months
). The significance of autoimmunity in NHL in a larger series of patients s
hould be investigated in future studies.