X. Troussard et al., PERSISTENT POLYCLONAL LYMPHOCYTOSIS WITH BINUCLEATED B-LYMPHOCYTES - A GENETIC PREDISPOSITION, British Journal of Haematology, 88(2), 1994, pp. 275-280
Persistent lymphocytosis is usually associated with a malignant lympho
proliferative disease (MLPD). We report six female patients presenting
a chronic, moderate lymphocytosis of 2-16 years duration with atypica
l binucleated lymphocytes on peripheral blood smears. Further investig
ation showed a polyclonal increase in serum IgM and HLA-DR7 phenotype
in ail patients. The B cells were polyclonal because Southern hybridiz
ation of DNA and polymerase chain reaction failed to demonstrate a clo
nal rearrangement of immunoglobulin heavy chain genes. Peripheral bloo
d examination showed binucleated lymphocytes in a family member of two
of the cases; taken together with the association with HLA-DR7 these
data suggest a genetic predisposition, The identification of this beni
gn syndrome is important in order to prevent its misdiagnosis as a MLP
D.