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Lancet ; 2(8408): 897-9, 1984 Oct 20.
Article in English | MEDLINE | ID: mdl-6148622

ABSTRACT

11/19 adults with a persistent increase in the total lymphocyte count, but with neither lymphodenopathy, hepatomegaly, nor splenomegaly, proved to have a monoclonal increase in B lymphocytes indicative of chronic lymphatic leukaemia (CLL). All remaining 8 patients had increased numbers of T-lymphocytes, more often of the helper than of the suppressor subsets. All the patients with a lymphocyte count in excess of 10 000/microliter, but only 5/13 patients with a lymphocyte count below 10 000/microliter had CLL. In adults a sustained lymphocytosis is thus not an adequate basis for the diagnosis of early CLL, which requires the demonstration of a monoclonal population. The T-lymphocytosis is likely to be reactive rather than neoplastic in nature.


Subject(s)
Leukemia, Lymphoid/immunology , Lymphocytosis/immunology , Adult , Aged , Antibodies, Monoclonal , B-Lymphocytes/immunology , Female , HLA-DR Antigens , Histocompatibility Antigens Class II/immunology , Humans , Leukemia, Lymphoid/complications , Leukemia, Lymphoid/diagnosis , Lymphocytosis/etiology , Male , Middle Aged , Rosette Formation , T-Lymphocytes/immunology
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