Da. Hansen et al., IDENTIFICATION OF MONOCLONAL IMMUNOGLOBULINS AND QUANTITATIVE IMMUNOGLOBULIN ABNORMALITIES IN HAIRY-CELL LEUKEMIA AND CHRONIC LYMPHOCYTIC-LEUKEMIA, American journal of clinical pathology, 102(5), 1994, pp. 580-585
Serum and urine samples from 161 cases of hairy cell leukemia (HCL) an
d 50 cases of chronic lymphocytic leukemia (CLL) were analyzed for mon
oclonal immunoglobulin (Mlg) by using a combination of high-resolution
protein electrophoresis, immunoelectrophoresis, and immunofixation. Q
uantitative immunoglobulin analysis also was performed on all serum sa
mples. Monoclonal immunoglobulin, usually of low intensity, was identi
fied in serum or urine in 26 (16.1%) cases of HCL compared with 27 (54
%) cases of CLL. Forty-eight (29.8%) cases of HCL had an increase in o
ne or more immunoglobulins; increases in IgG were the most frequent. I
n CLL, 48 (96.0%) cases had a decrease in one or more immunoglobulins,
with decreases in IgG, IgA, and IgM in 76%, 68%, and 56% of the cases
, respectively. The: correlation between serum or urine monoclonal imm
unoglobulin light chain and the surface membrane light chain was 88% i
n CLL. compared with 47.4% in I-ICL. These findings confirm previous o
bservations of frequent polyclonal hyper-gamma-globulinemia in HCL, hy
po-gamma-globulinemia in CLL, and weak monoclonal immunoglobulins in b
oth disorders. The contrasting immunoglobulin abnormalities in HCL and
CLL indicate distinctive biologic differences in these chronic B-cell
leukemias.