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IgE 多发性骨髓瘤:临床实验室检测的矛盾结果。

An IgE multiple myeloma: contradictory findings in clinical laboratory testing.

机构信息

Department of Laboratory Medicine, University-Hospital of Padova, Italy.

出版信息

Clin Chim Acta. 2013 Oct 21;425:114-6. doi: 10.1016/j.cca.2013.07.006. Epub 2013 Jul 17.

Abstract

BACKGROUND

IgE multiple myeloma is a rare kind of plasma cell disorder, characterized by an aggressive clinical course, where laboratory testing plays a fundamental role for the correct diagnosis in order to start a targeted therapy. In the present paper it is described a case of IgE myeloma where contradictory findings between immunometric and separative techniques were found.

MATERIALS AND METHODS

Serum and 24h urine samples were tested using electrophoresis and immunofixation electrophoresis employing IgE antiserum and IgE were quantified using an immunometric method.

RESULTS

Serum immunofixation evidenced a monoclonal band ascribable to IgE lambda and IgE serum concentration was 1,364,00 kU/L. Urine electrophoresis evidenced a band compatible with IgE, and urine concentration was 2715 kU/L. On the contrary in the immunofixation of the urine sample no band reacting with IgE antiserum was found.

CONCLUSIONS

Considering that the immunometric method measured IgE in urine sample and the electrophoresis of urine sample evidenced a band compatible with IgE, the explanation could be that during renal filtration or because of some characteristics related to urine matrix, the immunoglobulin IgE could had been modified in the site recognized by the antiserum used in immunofixation, and not in the one used in the immunometric method.

摘要

背景

IgE 多发性骨髓瘤是一种罕见的浆细胞疾病,其临床病程具有侵袭性,实验室检测在正确诊断中起着至关重要的作用,以便开始靶向治疗。本文描述了一例 IgE 骨髓瘤病例,该病例的免疫比浊法和分离技术检测结果存在矛盾。

材料与方法

采用电泳和免疫固定电泳法检测血清和 24 小时尿液样本,使用 IgE 抗血清进行免疫检测,并采用免疫比浊法对 IgE 进行定量。

结果

血清免疫固定电泳显示可归因于 IgE λ的单克隆带,IgE 血清浓度为 1364000 kU/L。尿电泳显示与 IgE 相匹配的条带,尿浓度为 2715 kU/L。相反,在尿液样本的免疫固定中,未发现与 IgE 抗血清反应的条带。

结论

考虑到免疫比浊法检测了尿液样本中的 IgE,且尿液样本的电泳显示与 IgE 相匹配的条带,其解释可能是在肾小球滤过过程中,或由于与尿液基质相关的某些特性,免疫球蛋白 IgE 在免疫固定中抗血清识别的部位发生了修饰,而不是在免疫比浊法中使用的部位。

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