A Case of Clinical Confusion Due to Erroneous M-protein Quantifications: To Splice or Skim?

Pak Cheung Chan, Amir Karin, Signy Chow
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Abstract

An M-protein identified on electrophoresis is conventionally quantified by integrating the M-spike from baseline (PD), invariably including some irrelevant/background proteins. The use of an alternative approach that skims the M-spike tangentially thereby excluding the background proteins (TS), however, has been scanty. We report herein a case in which PD overestimated the M-proteins inconsistently, leading to confusion over relapse in a multiple myeloma patient. At diagnosis, a 65-year old male had an IgG kappa M-spike of 44 g/L which decreased to 6 g/L (PD) following chemotherapy. Six weeks after autologous stem cell transplantation (ASCT), two M-spikes measuring respectively 10 and 5 g/L emerged. Together with decreases in hemoglobin and blood cell counts, a relapse was suspected. Bone marrow examinations, however, did not reveal any significant plasmacytosis or clonal restriction. Re-analyses by TS reduced the original M-protein estimations by 12% and 88% pre- and post-ASCT respectively, and corroborated the disease activity/status consistently.

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错误的m蛋白定量导致临床混淆:剪接还是脱脂?
在电泳上鉴定的m蛋白通常是通过整合基线(PD)的m峰来定量的,其中总是包括一些不相关的/背景蛋白。然而,使用一种替代方法,即从切线上剥离m突,从而排除背景蛋白(TS),目前还很少。我们在此报告一个病例,PD高估m蛋白不一致,导致多发性骨髓瘤患者复发混淆。确诊时,65岁男性IgG kappa m峰值为44 g/L,化疗后降至6 g/L (PD)。自体干细胞移植(ASCT) 6周后,出现两个m -尖峰,分别为10和5 g/L。再加上血红蛋白和血细胞计数的减少,怀疑是复发。然而,骨髓检查未发现任何明显的浆细胞病或克隆限制。通过TS重新分析,asct前和asct后的m蛋白估定值分别降低了12%和88%,并一致地证实了疾病的活动/状态。
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