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土耳其慢性淋巴细胞白血病患者一级亲属中单克隆B淋巴细胞增多症的患病率。

Prevalence of monoclonal B lymphocytosis in first-degree relatives of chronic lymphocytic leukemia patients in Turkey.

作者信息

Demirci Taner, Yeğin Zeynep Arzu, Kurşunoğlu Nevruz, Yılmaz Zeynep, Suyanı Elif, Özkurt Zübeyde Nur, Yağcı Münci

机构信息

Gazi University Faculty of Medicine, Department of Internal Medicine, Ankara, Turkey. E-mail:

出版信息

Turk J Haematol. 2015 Mar 5;32(1):29-34. doi: 10.4274/tjh.2013.0288.

Abstract

OBJECTIVE

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.

MATERIALS AND METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

目的

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。

材料与方法

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。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87a5/4439904/c2ff63c2a930/TJH-32-29-g2.jpg

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