R. Delage et al., MULTIPLE BCL-2 IG GENE REARRANGEMENTS IN PERSISTENT POLYCLONAL B-CELLLYMPHOCYTOSIS/, British Journal of Haematology, 97(3), 1997, pp. 589-595
Persistent polyclonal B-cell lymphocytosis is a benign lymphoprolifera
tive disorder of unknown aetiology occurring exclusively in women, cha
racterized by typical binucleated lymphocytes, polyclonal expansion of
B cells and elevated serum IgM. Owing to the role of Bcl-2 oncogene i
n inhibition of apoptosis, we have investigated the presence of the bc
l-2/Ig gene rearrangement. Bcl-2/Ig gene rearrangement was determined
by polymerase chain reaction targeting the usual breakpoint regions of
the t(14;18). Bcl-2/Ig gene rearrangement was identified in all six p
atients and, more importantly, multiple rearrangements were present in
five patients. The frequency of the bcl-2/Ig gene rearrange ment is e
stimated to be of one translocation in 1 x 10(2) to 1 x 10(3) peripher
al blood mononuclear cells. We conclude that persistent polyclonal B-c
ell lymphocytosis is associated with bcl-2/Ig gene rearrangement. Thes
e findings are of clinical importance because these patients may be mi
sdiagnosed as having a leukaemic expression of non-Hodgkin's lymphoma.