Monoclonal B-cell lymphocytosis

被引:11
|
作者
Maitre, Elsa [1 ]
Troussard, Xavier [1 ]
机构
[1] CHU Caen Normandie, Lab Hematol Biol, Ave Cote Nacre, F-14033 Caen 9, France
关键词
Monoclonal B-Cell lymphocytosis; Chronic lymphocytic leukemia; Flow cytometry; Progression; NATURAL-HISTORY; PERIPHERAL-BLOOD; NOTCH1; MUTATIONS; SCORING SYSTEM; FLOW-CYTOMETRY; LEUKEMIA; COUNT; INDIVIDUALS; RISK; MBL;
D O I
10.1016/j.beha.2019.06.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Flow cytometry diagnostic practices can detect very low levels of clonal B cells in the peripheral blood. In the absence of clinical symptoms, cytopenia or organomegaly, the small clones may correspond to monoclonal B-cell leukemia (MBL) diagnosis. Most MBLs harbor a chronic lymphocytic leukemia (CLL) phenotype (e.g., CD5+, CD23(+)) and are referred to as CLL-type MBL. The two other types are atypical CLL-type MBL and non-CLL-type MBL. In addition to the phenotypical classification, the clonal B count is a major issue because of the impact on the prognosis and the risk of progression in CLL. It allows for the discrimination of two distinct types: high-count (HC) MBL and low-count (LC)-MBL based on a cutoff value of 0.5 x 10(9)/L clonal B cells. LC MBL appears to be very stable over time and is probably related to immunosenescence. Conversely, HC MBL could be a premalignant state before the occurrence of CLL.
引用
收藏
页码:229 / 238
页数:10
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