Mono-dysplasia score based on automated cell counter (Sysmex) – A novel parameter for differentiating reactive monocytosis from hematological malignancies

Q4 Medicine
Sabina Langer, Priyanka Moule, Nitin Gupta, Jyoti Kotwal
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引用次数: 0

Abstract

INTRODUCTION: In India, there is a high burden of infections such as tuberculosis, dengue, and malaria which are common causes of monocytosis. This increases the workload of smear examination by the pathologist. “Mono-dysplasia score” is obtained with a simple complete blood count on an automated cell counter and includes the parameters neutrophil (Ne) and monocyte (Mo) count and Ne-WX which is a Ne dispersion parameter. It is operator independent, objective, and does not require a high level of expertise.AIMS: The aims of the study were to assess the utility of Monoscore/mono-dysplasia score calculated using research parameters of Sysmex XN automated cell counter, as a screening tool for differentiating reactive monocytosis from hematological malignancies associated with monocytosis.MATERIALS AND METHODS: Samples sent in EDTA vacutainer for routine hemogram fulling the criteria for monocytosis (WHO criteria – absolute monocyte count ≥1 × 109/L and accounting for ≥10% of the total white blood cell count) were included in the study. Monoscore was calculated using the formula established by Schillinger et al. Flow cytometry, bone marrow examination, etc., were done as and when needed as standard-of-care tests to establish a final diagnosis.RESULTS: One thousand two hundred and fifty-seven samples were analyzed out of which 41 samples were chronic myelomonocytic leukemia and 126 were other hematological malignancies (HD) including acute leukemias, myelodysplastic syndrome, myeloproliferative neoplasm, etc. Using receiver operating characteristics curves, we established the cutoff 0.212 which showed a sensitivity of 97.6% and specificity of 96.4% to differentiated reactive monocytosis form HD.CONCLUSIONS: A sample showing monocytosis and Monoscore <0.212 and without any other flags can be safely auto-authorized without peripheral blood smears examination, reducing the burden of slides to be reviewed.
基于自动细胞计数器(Sysmex)的单核细胞发育不良评分——一种区分反应性单核细胞增多症和血液系统恶性肿瘤的新参数
简介:在印度,结核病、登革热和疟疾等感染的负担很高,这些感染是单核细胞增多症的常见原因。这增加了病理学家涂片检查的工作量。“单核发育不良评分”是通过在自动细胞计数器上进行简单的全血细胞计数获得的,包括中性粒细胞(Ne)和单核细胞(Mo)计数参数以及Ne- wx (Ne弥散参数)。它是操作员独立的,客观的,不需要高水平的专业知识。目的:该研究的目的是评估使用Sysmex XN自动细胞计数器的研究参数计算的Monoscore/单核发育不良评分的效用,作为区分反应性单核细胞增多症和与单核细胞增多症相关的血液恶性肿瘤的筛选工具。材料和方法:在EDTA抽真空器中送去的符合单核细胞增多标准的常规血影样本(WHO标准-绝对单核细胞计数≥1 × 109/L,占白细胞总数≥10%)被纳入研究。Monoscore采用Schillinger等人建立的公式计算。流式细胞术,骨髓检查等,在需要时作为标准治疗试验进行,以确定最终诊断。结果:共分析样本1257份,其中慢性髓细胞白血病41份,其他血液病126份,包括急性白血病、骨髓增生异常综合征、骨髓增生性肿瘤等。根据受试者工作特征曲线,我们建立了临界值0.212,对HD型分化性反应性单核细胞增多症的敏感性为97.6%,特异性为96.4%。结论:显示单核细胞增多且Monoscore <0.212且无任何其他标记的样本可以在不进行外周血涂片检查的情况下安全地自动获得批准,减少了需要审查的载玻片的负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Applied Hematology
Journal of Applied Hematology Medicine-Hematology
CiteScore
0.40
自引率
0.00%
发文量
34
审稿时长
24 weeks
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