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采用有限的浆细胞流式细胞术检测组合并进行CD138免疫组化复检,是评估骨髓标本中浆细胞肿瘤的最佳工作流程。

A limited plasma cell flow cytometry panel with reflex CD138 immunohistochemistry is an optimal workflow process for evaluating plasma cell neoplasms in bone marrow specimens.

作者信息

Chen Zhongchuan Will, Perkins Sherrie L, Weiss Ronald L, Bahler David W, Hussong Jerry W, Salama Mohamed E

机构信息

From the Division of Hematopathology, ARUP Laboratories/University of Utah, Salt Lake City.

出版信息

Am J Clin Pathol. 2015 Jan;143(1):78-83. doi: 10.1309/AJCP3HKHEN8DFIPO.

Abstract

OBJECTIVES

To determine the optimal workflow combination of flow cytometry (FC) and immunohistochemistry tests for efficient and cost-effective evaluation of plasma cell (PC) neoplasms (PCNs) in bone marrow (BM) specimens.

METHODS

Various workflow combinations of immunohistochemistry and FC for 4,031 BM specimens worked up for PCNs were compared. Turnaround time (TAT), immunohistochemistry usage, technical charges, and addendum/amendment rates were compared between periods to determine the optimal workflow combination.

RESULTS

Five distinct workflow periods were identified, with varying combinations of full or limited FC panels for assessing PC clonality and CD138/κ/λ immunohistochemistry for PC quantification. Replacement of full FC with limited FC was associated with significant reductions in TAT and number of immunostains performed per case. Elimination of immunohistochemistry on cases determined to be polyclonal by FC also resulted in significant reductions in immunohistochemistry usage and significant cost savings.

CONCLUSIONS

Assessment of PC clonality using a limited FC panel followed by reflex CD138 immunohistochemistry on cases that are monoclonal by FC provides an optimal and cost-effective workflow for evaluating PCNs in BM samples.

摘要

目的

确定流式细胞术(FC)和免疫组织化学检测的最佳工作流程组合,以便对骨髓(BM)标本中的浆细胞(PC)肿瘤(PCNs)进行高效且具有成本效益的评估。

方法

比较了针对4031份进行PCNs检查的BM标本的免疫组织化学和FC的各种工作流程组合。比较了不同时期的周转时间(TAT)、免疫组织化学使用情况、技术费用以及补充/修正率,以确定最佳工作流程组合。

结果

确定了五个不同的工作流程时期,评估PC克隆性的全FC或有限FC检测组合以及用于PC定量的CD138/κ/λ免疫组织化学组合各不相同。用有限FC替代全FC可显著缩短TAT,并减少每个病例进行的免疫染色数量。对于FC确定为多克隆的病例,取消免疫组织化学检测也可显著减少免疫组织化学的使用,并节省大量成本。

结论

使用有限FC检测组合评估PC克隆性,随后对FC检测为单克隆性的病例进行CD138免疫组织化学检测,为评估BM样本中的PCNs提供了一种最佳且具有成本效益的工作流程。

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