[细胞质轻链免疫荧光结合骨髓涂片 FISH 检测多发性骨髓瘤细胞遗传学异常]。

Y Shi, H Yang, R Guo, Z Guo, J Y Li, Y J Wu, H R Qiu
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摘要

目的分析细胞质轻链免疫荧光与骨髓涂片荧光原位杂交(新FISH)检测多发性骨髓瘤(MM)细胞遗传学异常的敏感性。方法:选取2022年4月至2023年10月南京医科大学第一附属医院收治的42例MM患者作为研究对象。采用新型FISH和CD138免疫磁珠分选技术结合FISH(MACS-FISH)或细胞质免疫球蛋白FISH(cIg-FISH)检测多发性骨髓瘤患者的细胞遗传学异常,使用1q21/1p32、p53、IgH、IgH/FGFR3 [t (4;14) ]和IgH/MAF [t (14;16) ]等组合探针分析细胞遗传学检测结果。结果显示在23例MM患者中,cIg-FISH和新FISH的异常检出率分别为95.7%和100.0%(P>0.05)。cIg-FISH和新FISH对1q21+、1p32-、p53缺失和IgH异常的检出率一致,分别为52.2%、8.7%、17.4%和65.2%。两种方法进一步对有 IgH 异常的 t(4;14)和 t(14;16)患者进行检测的结果相同。t(4;14)的阳性率为 26.7%,而 t(14;16)则未检出。在 19 例 MM 患者中,MACS-FISH 和新 FISH 的异常检出率分别为 73.7% 和 63.2%(P>0.05)。MACS-FISH检测到的1q21+、1p32-和IgH异常的阳性率略高于新FISH检测到的阳性率,但差异无统计学意义(所有P值均大于0.05)。结论新 FISH 方法对 MM 患者细胞遗传学异常的检出率更高,且与 MACS-FISH 和 cIg-FISH 具有良好的一致性。
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[Cytoplasmic light-chain immunofluorescence combined with FISH in bone marrow smears to detect cytogenetic abnormalities in multiple myeloma].

Objective: To analyze the sensitivity of cytoplasmic light-chain immunofluorescence with fluorescence in situ hybridization in bone marrow smears (new FISH) for detecting cytogenetic abnormalities in multiple myeloma (MM) . Methods: 42 MM patients admitted to the First Affiliated Hospital of Nanjing Medical University from April 2022 to October 2023 were enrolled. The patients with MM were detected by new FISH and CD138 immunomagnetic bead sorting technology combined with FISH (MACS-FISH) or cytoplasmic immunoglobulin FISH (cIg-FISH) to analyze cytogenetic detection results using combination probes which included 1q21/1p32, p53, IgH, IgH/FGFR3 [t (4;14) ], and IgH/MAF [t (14;16) ]. Results: In 23 patients with MM, the abnormality detection rates of cIg-FISH and new FISH were 95.7% and 100.0%, respectively (P>0.05). The detection rates of 1q21+, 1p32-, p53 deletion, and IgH abnormalities by cIg-FISH and new FISH were consistent, which were 52.2%, 8.7%, 17.4%, and 65.2%, respectively. The results of the two methods further performed with t (4;14) and t (14;16) in patients with IgH abnormalities were identical. The positive rate of t (4;14) was 26.7%, whereas t (14;16) was not detected. In 19 patients with MM, the abnormality detection rates of MACS-FISH and new FISH were 73.7% and 63.2%, respectively (P>0.05). The positivity rate of 1q21+, 1p32- and IgH abnormalities detected by MACS-FISH were slightly higher than those detected by new FISH; however, the differences were not statistically significant (all P values >0.05) . Conclusion: The new FISH method has a higher detection rate of cytogenetic abnormalities in patients with MM and has good consistency with MACS-FISH and cIg-FISH.

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