Detection of a monoclonal B-cell population in the peripheral blood with overall kappa:lambda ratio > 3:1 or < 0.3:1, or greater than 25% of B cells lacking or expressing low level surface immunoglobulin or a disease-specific immunophenotype.
Repeat assessment should demonstrate that the monoclonal B-cell population is stable over a 3-month period. Exclusion criteria lymphadenopathy and organomegaly, or associated autoimmune/infectious disease, or B-lymphocyte count >5 × 109/L, or any other feature diagnostic of a B-lymphoproliferative disorder. However, a paraprotein may be present or associated with MBL and should be evaluated independently.
Sub-classification: CD5+23+: this is the major subcategory and corresponds to a CLL immunophenotype (Cheson et al, 1996). CD5+23−: correlate moderate level of CD20 and CD79b expression with atypical CLL. CD5−: corresponds to non-CLL lymphoproliferative disorder
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