Demirci Taner, Yeğin Zeynep Arzu, Kurşunoğlu Nevruz, Yılmaz Zeynep, Suyanı Elif, Özkurt Zübeyde Nur, Yağcı Münci
Gazi University Faculty of Medicine, Department of Internal Medicine, Ankara, Turkey. E-mail:
Turk J Haematol. 2015 Mar 5;32(1):29-34. doi: 10.4274/tjh.2013.0288.
Monoclonal B lymphocytosis (MBL) is considered to be a precursor state for chronic lymphocytic leukemia (CLL). This study was planned to evaluate the MBL prevalence in first-degree relatives of CLL patients in Turkey, which is considered to be an ethnic and geographic bridge between the Eastern and Western worlds.
A total of 136 volunteers [median age: 40 (17-77) years; male/female: 60/76] from 61 families were included. Flow cytometry analysis by 4-colour staining was used for MBL diagnosis.
MBL was demonstrated in 17 cases (12.5%). A total of 14 cases (10.3%) were classified as CLL-like MBL, while 3 (2.2%) exhibited a non-CLL-like phenotype. The prevalence of MBL was 12.72% in subjects aged less than 40 years, 12.28% in subjects between 40 and 60 years, and 40% in subjects over 60 years, without statistical significance (p>0.05). A total of 115 cases were evaluated for intermarriage, which was observed in 19 cases (16.5%). The prevalence of MBL did not differ based on intermarriage status (p>0.05).
The current report is the first MBL prevalence study in a Eurasian population that demonstrates a similar distribution pattern of MBL in Anatolian CLL kindreds. Further efforts should be made to refine our understanding of the natural history and clinical outcomes of MBL.
单克隆B淋巴细胞增多症(MBL)被认为是慢性淋巴细胞白血病(CLL)的前驱状态。本研究旨在评估土耳其CLL患者一级亲属中MBL的患病率,土耳其被视为东西方之间的种族和地理桥梁。
纳入了来自61个家庭的136名志愿者[中位年龄:40(17 - 77)岁;男性/女性:60/76]。采用四色染色的流式细胞术分析进行MBL诊断。
17例(12.5%)检测到MBL。共14例(10.3%)被归类为CLL样MBL,而3例(2.2%)表现为非CLL样表型。年龄小于40岁的受试者中MBL患病率为12.72%,40至60岁的受试者中为12.28%,60岁以上的受试者中为40%,差异无统计学意义(p>0.05)。共对115例进行了异族通婚评估,其中19例(16.5%)存在异族通婚。MBL患病率在异族通婚状态方面无差异(p>0.05)。
本报告是在欧亚人群中进行的首次MBL患病率研究,显示安纳托利亚CLL亲属中MBL的分布模式相似。应进一步努力加深我们对MBL自然史和临床结局的理解。