The Missing M Band: Is it Really Non Secretory Multiple Myeloma?

Q2 Medicine
Mala Mahto, Anurag Kumar, Neha Rai, Visesh Kumar, Subhash Kumar, Tarun Kumar, Ruchi Sinha, Pritanjali Singh
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引用次数: 0

Abstract

Background: Non-secretory multiple myeloma (NSMM) is defined as clonal bone marrow plasma cells ≥10% or biopsy proven plasmacytoma, evidence of end-organ damage due to underlying plasma cell dyscrasia, namely hypercalcemia, renal insufficiency, anaemia, bone lesions and lack of serum and urinary monoclonal protein on electrophoresis and immunofixation. They represent 3-5% of multiple myeloma (MM). With the advent of serum free light chain (s FLC) measurement, most of NSMMs have been classified as Light chain Multiple myeloma (LCMM). Thus, the proportion of true NSMM, meaning MM that secretes no monoclonal protein (complete immunoglobulin, heavy or light chain) is close to 1-2% of all myelomas. There is a need to distinguish between the true non-secretory from the other forms of oligo-secretory (OSMM) and secretory form of myeloma like LCMM with use of advanced diagnostic tools such as s FLC assay as the former has a good prognosis.

Case presentation: We discuss a case of a 65-years-old female who presented with chronic chest pain since one year. Cardiac and musculoskeletal involvement were ruled out. Monoclonal gammopathy was suspected in view of imaging abnormalities. Surprisingly, SPE and IFE reported absence of M band. A provisional diagnosis of NSMM was made based on biopsy features. However, diagnosis of NSMM was later changed to LCMM in view of a positive sFLC ratio.

Conclusions: It is well-known that the sequence of diagnostic investigations plays a crucial role in the timely diagnosis and management of patients. However, in this case it was a faulty sequence of ordering investigations which prolonged the hospital stay and delayed therapeutic intervention for the patient concerned. Serum Protein Electrophoresis (SPE), Immunofixation electrophoresis (IFE) and sFLC are simple blood-based tests which can help diagnose a majority of cases of monoclonal gammopathies. They need to be included as first line tests in our approach to evaluating a suspected case of monoclonal gammopathy.

缺失的M带:真的是非分泌性多发性骨髓瘤吗?
背景:非分泌性多发性骨髓瘤(NSMM)被定义为克隆性骨髓浆细胞≥10%或活检证实的浆细胞瘤,终末器官损伤的证据是由于潜在的浆细胞病变,即高钙血症、肾功能不全、贫血、骨病变以及电泳和免疫固定显示血清和尿单克隆蛋白缺乏。它们占多发性骨髓瘤(MM)的3-5%。随着血清游离轻链(FLC)测定的出现,大多数NSMMs已被归类为轻链多发性骨髓瘤(LCMM)。因此,真正的NSMM,即不分泌单克隆蛋白(完整免疫球蛋白,重链或轻链)的MM的比例接近所有骨髓瘤的1-2%。由于前者具有良好的预后,因此需要使用先进的诊断工具(如FLC检测)来区分真正的非分泌性骨髓瘤,即其他形式的低分泌性骨髓瘤(OSMM)和分泌性骨髓瘤(如LCMM)。病例介绍:我们讨论了一个65岁的女性谁提出了慢性胸痛一年。排除了心脏和肌肉骨骼的影响。鉴于影像学异常,怀疑为单克隆伽玛病。令人惊讶的是,SPE和IFE报告了M波段的缺失。根据活检特征作出NSMM的临时诊断。然而,鉴于sFLC比例阳性,NSMM的诊断后来改为LCMM。结论:诊断检查顺序对患者的及时诊断和治疗起着至关重要的作用。然而,在这个案例中,是错误的调查顺序延长了住院时间,延误了对有关病人的治疗干预。血清蛋白电泳(SPE),免疫固定电泳(IFE)和sFLC是简单的血液检测,可以帮助诊断大多数单克隆伽马病病例。在我们评估单克隆γ病疑似病例的方法中,它们需要作为一线测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
2.30
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