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CLLflow 评分的实用性。

Usefulness of the CLLflow score.

机构信息

Hematology Laboratory, ICO-Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, Josep Carreras Leukemia Research Institute, Badalona, Spain.

出版信息

Cytometry B Clin Cytom. 2018 Nov;94(6):950-952. doi: 10.1002/cyto.b.21623. Epub 2018 Jan 19.

DOI:10.1002/cyto.b.21623
PMID:29316199
Abstract

BACKGROUND

The CLLflow score was recently suggested as an improvement over the Moreau score (MS) for the diagnosis and classification of B-cell lymphoproliferative disorders (B-LPD).

METHODS

We determined the CLLflow score in peripheral blood or bone marrow of a series of cases with an inconclusive immunophenotype, including samples with a MS of 3 (n = 52) and CD5-positive with a score of 2 (n = 38). As controls, B-LPD with a MS of 0-1 (n = 95), CD5-negative score 2 (n = 24), and score 4-5 (i.e., chronic lymphocytic leukemia [CLL], n = 166) were included.

RESULTS

The CLLflow score was positive (suggestive of CLL) in all CLL cases and negative in all MS <2, regardless of CD200-positivity, which occurred in 31% (29/95) of cases. The CLLflow score was positive in 71%, 29%, and 8% of samples with a MS 3, CD5-positive score 2, and CD5-negative score 2, respectively.

DISCUSSION

Our results suggest that the CLLflow is useful in the differential diagnosis of cases with inconclusive immunophenotype. © 2018 International Clinical Cytometry Society.

摘要

背景

CLLflow 评分最近被提议作为对 Moreau 评分(MS)的改进,用于诊断和分类 B 细胞淋巴增殖性疾病(B-LPD)。

方法

我们在一系列免疫表型不确定的病例的外周血或骨髓中确定了 CLLflow 评分,包括 MS 为 3 的样本(n=52)和 CD5 阳性且评分 2 的样本(n=38)。作为对照,MS 为 0-1 的 B-LPD(n=95)、CD5 阴性评分 2(n=24)和评分 4-5(即慢性淋巴细胞白血病 [CLL],n=166)的 B-LPD 也被包括在内。

结果

所有 CLL 病例的 CLLflow 评分均为阳性(提示 CLL),而所有 MS<2 的病例均为阴性,无论 CD200 是否阳性,这在 31%(29/95)的病例中发生。MS 为 3、CD5 阳性评分 2 和 CD5 阴性评分 2 的样本中,CLLflow 评分分别为阳性的比例为 71%、29%和 8%。

讨论

我们的结果表明,CLLflow 有助于对免疫表型不确定的病例进行鉴别诊断。©2018 国际临床细胞化学学会。

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引用本文的文献

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CD200 and Chronic Lymphocytic Leukemia: Biological and Clinical Relevance.CD200与慢性淋巴细胞白血病:生物学及临床相关性
Front Oncol. 2020 Nov 26;10:584427. doi: 10.3389/fonc.2020.584427. eCollection 2020.