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脑脊液白细胞计数和蛋白水平在预测系统性侵袭性 B 细胞淋巴瘤脑膜侵犯中的价值。

Value of cerebrospinal fluid white cell count and protein level in predicting leptomeningeal involvement by systemic aggressive B-cell lymphoma.

机构信息

Department of Pathology and Laboratory Medicine, Auckland District Health Board, Auckland, New Zealand.

出版信息

Int J Lab Hematol. 2022 Jun;44(3):490-496. doi: 10.1111/ijlh.13815. Epub 2022 Feb 15.

Abstract

INTRODUCTION

Diagnostic cerebrospinal fluid (CSF) analysis for patients with newly diagnosed aggressive B-cell lymphoma at risk of secondary central nervous system involvement typically includes multiparametric flow cytometry (MFC), cytology (CC), white cell count (WCC) and total protein. The strength of relationships between MFC results and the remaining variables has been disputed in small studies. We explored these relationships in a large homogeneous cohort of patient samples, aiming to establish the relationship between WCC and protein level and MFC results.

METHODS

Adult patients with aggressive B-cell lymphoma at risk of CNS involvement who underwent staging CSF analysis by MFC were identified retrospectively from institutional electronic records between October 2011 and December 2020.

RESULTS

Three hundred and seventy eight samples, including 45 (11.9%) MFC+ samples, were analysed. The relative sensitivity of CC for MFC positivity was 0.38, with PPV of 0.68. Significantly higher median WCC (p < .001) and protein levels (p = .011) were seen in MFC+ vs. MFC- samples. MFC + CC+ (vs. MFC + CC- samples) demonstrated higher median neoplastic events and neoplastic cell concentration. WCC ≥36 × 10 /L and protein ≥1.12 g/L cut-off values demonstrated the highest PPVs for MFC positivity (0.67 and 0.88, respectively).

CONCLUSIONS

Statistically significant associations exist between elevated WCC and protein and MFC positivity, and selected WCC and protein cut-off values have PPVs comparable to that of cytological assessment. Whilst routine WCC and protein analysis may be unnecessary, WCC/protein values above these levels could be regarded as reasonable evidence of CSF involvement in the appropriate setting.

摘要

简介

对于有新发侵袭性 B 细胞淋巴瘤且有中枢神经系统受累风险的患者,诊断性脑脊液(CSF)分析通常包括多参数流式细胞术(MFC)、细胞学(CC)、白细胞计数(WCC)和总蛋白。在一些小型研究中,MFC 结果与其他变量之间的关系存在争议。我们在一个大型、同质的患者样本队列中探索了这些关系,旨在确定 WCC 和蛋白水平与 MFC 结果之间的关系。

方法

回顾性地从机构电子记录中确定了 2011 年 10 月至 2020 年 12 月期间因中枢神经系统受累风险而接受 MFC 分期 CSF 分析的侵袭性 B 细胞淋巴瘤成人患者。

结果

分析了 378 个样本,包括 45 个(11.9%)MFC+样本。CC 对 MFC 阳性的相对灵敏度为 0.38,PPV 为 0.68。与 MFC-样本相比,MFC+样本的中位 WCC(p<0.001)和蛋白水平(p=0.011)明显更高。MFC+CC+(与 MFC+CC-样本相比)显示更高的中位肿瘤事件和肿瘤细胞浓度。WCC≥36×10/L 和蛋白≥1.12 g/L 截断值对 MFC 阳性的 PPV 最高(分别为 0.67 和 0.88)。

结论

WCC 和蛋白升高与 MFC 阳性之间存在统计学显著关联,选定的 WCC 和蛋白截断值的 PPV 与细胞学评估相当。虽然常规的 WCC 和蛋白分析可能不是必需的,但在适当的情况下,高于这些水平的 WCC/蛋白值可被视为 CSF 受累的合理证据。

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