血清免疫固定的不典型发现:1例报告。

IF 1
Ameerah Davids, David F Keren, Annalise E Zemlin, Fatima B Fazel, David L Murray, Ernest Musekwa, Marizna Korf
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引用次数: 0

摘要

简介:多发性骨髓瘤(Multiple myeloma, MM)的特点是浆细胞异常增殖,导致独特的单克隆蛋白(m蛋白)过量产生。疑似MM需要通过血清蛋白电泳、血清免疫固定(SIFE)和血清游离轻链(SFLC)检测联合筛选m蛋白。在琼脂糖凝胶上,m蛋白表现为一个相对受限的条带,其中在2中的迁移是罕见的。方法:55岁男性肺结核患者表现为严重的腰痛。经检查,他表现为慢性疾病,结膜苍白。x光片显示椎体压缩性骨折。全血细胞计数证实贫血;然而,血清钙和肌酐水平不符合骨髓瘤定义事件标准。结果:血清蛋白电泳显示低γ球蛋白血症,SIFE显示异常的无限制κ染色在γ -2区。κ SFLC和κ:λ比值明显升高。骨髓检查显示约90%浆细胞增多症。尿免疫固定显示一个与κ SFLC不成比例的小的受限κ带。值得注意的是,基质辅助激光解吸/电离飞行时间质谱法仅鉴定出多克隆κ SFLC。讨论:考虑到SIFE上缺乏可识别的m蛋白,尿免疫固定的小κ限制,以及κ SFLCs的多克隆增加,患者的病情被管理为低分泌性MM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An atypical finding on serum immunofixation: a case report.

Introduction: Multiple myeloma (MM) is characterized by the abnormal proliferation of plasma cells, resulting in the overproduction of distinctive monoclonal proteins (M-protein). Suspected MM necessitates screening for M-protein through a combination of serum protein electrophoresis, serum immunofixation (SIFE), and serum free light chain (SFLC) determination. An M-protein appears as a relatively restricted band on agarose gel, where migration in ɑ-2 is rare.

Methods: A 55-year-old man with pulmonary tuberculosis presented with severe lower back pain. On examination, he appeared chronically ill, with conjunctival pallor. X-rays revealed vertebral compression fractures. The full blood count confirmed anemia; however, serum calcium and creatinine levels did not meet myeloma-defining event criteria.

Results: The serum protein electrophoresis revealed hypogammaglobulinemia, with the SIFE demonstrating unusual unrestricted κ staining in the ɑ-2 region. A markedly elevated κ SFLC and κ:λ ratio were found. Bone marrow examination demonstrated approximately 90% plasmacytosis. Urine immunofixation revealed a small, restricted κ band disproportionate to the κ SFLC. Notably, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry identified only polyclonal κ SFLC.

Discussion: Given the absence of a discernible M-protein on SIFE, a small κ restriction on urine immunofixation, and a polyclonal increase in κ SFLCs, the patient's condition is being managed as an oligosecretory MM.

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