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以出血倾向为表现的IgM型多发性骨髓瘤:一例免疫表型分析病例报告

IgM multiple myeloma presenting with bleeding tendency: a case report with immunophenotype analysis.

作者信息

Zheng Ling, Zeng Zhiyong, Lin Junfang, Chen Junmin

机构信息

Department of Hematology and Rheumatology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, P.R. China.

出版信息

Oncol Lett. 2011 Jan;2(1):55-57. doi: 10.3892/ol.2010.216. Epub 2010 Nov 23.

Abstract

IgM multiple myeloma (MM) is an extremely rare lymphoproliferative disease associated with an aggressive clinical course. However, the diagnosis of IgM MM may be complicated by Waldenstrom's macroglobulinemia (WM), particularly when clinical manifestations and morphological features are not typical. It is crucial to distinguish between IgM MM and WM as their prognoses and treatment strategies are different. We report a case of IgM MM presenting with bleeding tendency and an immunophenotype analysis using flow cytometry and immunohistochemistry. Bone marrow cells exhibited a typical phenotype for plasma cells, expressing monoclonal cytoplasmatic IgL-λ, CD38 and CD138 instead of pan-B cell antigens CD19, CD20 and CD22, which are characteristic of the typical immunophenotype of WM. Therefore, the diagnosis of IgM MM was confirmed in this case, highlighting the significance of detailed immuno-phenotypic evaluation when clinical and morphological features are atypical.

摘要

IgM型多发性骨髓瘤(MM)是一种极其罕见的淋巴增殖性疾病,临床病程进展迅速。然而,IgM型MM的诊断可能会因华氏巨球蛋白血症(WM)而变得复杂,尤其是当临床表现和形态学特征不典型时。区分IgM型MM和WM至关重要,因为它们的预后和治疗策略不同。我们报告一例表现为出血倾向的IgM型MM病例,并使用流式细胞术和免疫组织化学进行免疫表型分析。骨髓细胞表现出浆细胞的典型表型,表达单克隆细胞质IgL-λ、CD38和CD138,而非WM典型免疫表型所特有的泛B细胞抗原CD19、CD20和CD22。因此,该病例确诊为IgM型MM,凸显了在临床和形态学特征不典型时进行详细免疫表型评估的重要性。

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本文引用的文献

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Multiple myeloma.多发性骨髓瘤
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Am J Hematol. 1998 Dec;59(4):302-8. doi: 10.1002/(sici)1096-8652(199812)59:4<302::aid-ajh6>3.0.co;2-z.
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