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HERO ID
520581
Reference Type
Journal Article
Title
Monoclonal B-cell lymphocytosis: definitions and natural history
Author(s)
Shanafelt, T; Hanson, CA
Year
2009
Is Peer Reviewed?
1
Journal
Leukemia and Lymphoma
ISSN:
1042-8194
Volume
50
Issue
3
Page Numbers
493-497
Language
English
DOI
10.1080/10428190902763483
Abstract
The diagnostic term monoclonal B-cell lymphocytosis (MBL) is used to characterise individuals with a circulating population of clonal B-cells, a total B-cell count of 5109/L, and no other features of a B-cell lymphoproliferative disorder. The clinical implications of MBL may differ depending on whether an individual with a normal lymphocyte count is identified via a screening assay (screening MBL) or identified through clinical evaluation of lymphocytosis (clinical MBL). The B-cell count used to distinguish between clinical MBL (5109/L) and CLL (5109/L) was selected largely based on tradition and technological advances and it is unknown whether the natural history of 'clinical MBL' differs from that of patients with Rai stage 0 CLL. Since, a diagnosis of 'leukemia' may lead to profound psychologic distress for patients, we believe the diagnosis of CLL should be based on an individual's risk of developing symptoms, requiring chemotherapeutic treatment and/or dying of disease. Additional studies are needed to determine whether the clinical outcome of patients with MBL differs from that of patients with Rai stage 0 CLL and to identify what B-cell threshold optimally distinguishes between these conditions.
Keywords
Monoclonal B-cell lymphocytosis; chronic lymphocytic leukemia; small; lymphocytic lymphoma; diagnosis; outcome; quality-of-life; leukemia; classification; progression; evolution; health; blood; cll
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