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通过单管流式细胞术分析提高对前体 B 淋巴细胞白血病中血幼粒细胞的识别。

Improved Recognition of Hematogones From Precursor B-Lymphoblastic Leukemia by a Single Tube Flow Cytometric Analysis.

机构信息

Department of Pathology, Cedars-Sinai Medical Center, Los Angeles, CA.

出版信息

Am J Clin Pathol. 2020 May 5;153(6):790-798. doi: 10.1093/ajcp/aqaa007.

DOI:10.1093/ajcp/aqaa007
PMID:32068791
Abstract

OBJECTIVES

To improve diagnostic accuracy in differentiating hematogones from leukemic blasts in cases of precursor B-lymphoblastic leukemia/lymphoma (B-ALL), particularly those that are posttreatment or after bone marrow transplant, and to provide an algorithmic approach to this diagnostic challenge.

METHODS

A seven-color antibody panel including CD10, CD19, CD45, CD38, CD34, CD58, and CD81 was generated to assess the feasibility of a single tube panel and provide an algorithmic approach to distinguish hematogones from B-ALL. Fifty-three cases were analyzed, and results were correlated with histology and ancillary studies.

RESULTS

There was a significant difference in mean fluorescent intensity (MFI) for CD81 and CD58 when comparing hematogones and B-ALL populations (P < .001). B-ALL cases had a mean (SD) MFI of 24.6 (27.5; range, 2-125) for CD81 and 135.6 (72.6; range, 48-328) for CD58. Hematogones cases had a mean (SD) MFI of 70.2 (19.2; range, 42-123) for CD81 and 38.8 (9.4; range, 23-58) for CD58.

CONCLUSIONS

The flow cytometry panel with the above markers and utilization of the proposed algorithmic approach provide differentiation of hematogones from B-ALL. This includes rare cases of hematogones and B-ALL overlap where additional ancillary studies are necessary.

摘要

目的

提高鉴别前体 B 淋巴细胞白血病/淋巴瘤(B-ALL)中造血细胞与白血病细胞的诊断准确性,尤其是治疗后或骨髓移植后的病例,并提供一种解决这一诊断难题的算法。

方法

采用包括 CD10、CD19、CD45、CD38、CD34、CD58 和 CD81 七种抗体的组合,评估单管面板的可行性,并提供一种算法来区分造血细胞和 B-ALL。分析了 53 例病例,并将结果与组织学和辅助研究相关联。

结果

在比较造血细胞和 B-ALL 群体时,CD81 和 CD58 的平均荧光强度(MFI)有显著差异(P<0.001)。B-ALL 病例的 CD81 和 CD58 的平均(SD)MFI 分别为 24.6(27.5;范围,2-125)和 135.6(72.6;范围,48-328)。造血细胞病例的 CD81 和 CD58 的平均(SD)MFI 分别为 70.2(19.2;范围,42-123)和 38.8(9.4;范围,23-58)。

结论

该流式细胞术组合标记物和提出的算法能够区分造血细胞和 B-ALL,包括罕见的造血细胞和 B-ALL 重叠病例,需要进一步进行辅助研究。

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