Monoclonal B-cell lymphocytosis (MBL): Biology, natural history and clinical management Review uri icon

Overview

MeSH Major

  • B-Lymphocytes
  • Lymphocytosis

abstract

  • Chronic lymphocytic leukemia (CLL) and the other low-grade non-Hodgkin lymphomas are among the most common lymphoid malignancies. Recent studies suggest that more than 4% of the general population over age 40 harbor a population of clonal B cells with the phenotype of either CLL or another B-cell malignancy, a condition now designated monoclonal B-cell lymphocytosis (MBL). Although all cases of CLL appear to be preceded by MBL, the majority of individuals with MBL will not develop a hematologic malignancy. The biologic characteristics and clinical implications of MBL appear to differ based on whether it is identified during the diagnostic evaluation of lymphocytosis or incidentally discovered through screening of individuals with normal lymphocyte counts as part of research studies using highly sensitive detection methods. In this paper, we provide a state of the art review on the prevalence, nomenclature, biology, natural history and clinical management of MBL.

publication date

  • March 2010

Research

keywords

  • Review

Identity

Language

  • eng

PubMed Central ID

  • PMC3913172

Digital Object Identifier (DOI)

  • 10.1038/leu.2009.287

PubMed ID

  • 20090778

Additional Document Info

start page

  • 512

end page

  • 20

volume

  • 24

number

  • 3