Dutcher bodies and Russell bodies in a case of t(11;14) multiple myeloma

IF 3.8 2区 医学 Q1 HEMATOLOGY British Journal of Haematology Pub Date : 2024-11-14 DOI:10.1111/bjh.19890
Jing Wu, Wei Cai, Mi Jiang
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Abstract

A 65-year-old woman presented with back pain. Serum immunofixation electrophoresis demonstrated immunoglobulin G (IgG) kappa type monoclonal protein. Bone marrow aspirate showed 41% abnormal plasma cells with different sizes, regular or irregular nuclei, most of which contained pink or colourless Dutcher bodies overlying nuclei entirely or partly (upper images, Dutcher bodies indicated by black arrows, Wright stain, ×100 objective) or/and Russell bodies within cytoplasm (upper images, Russell bodies indicated by red arrows). Bone marrow biopsy revealed pink Dutcher and Russell bodies in haematoxylin and eosin stain (bottom left image). Flow cytometry analysis showed the plasma cells to be clonal (bottom middle and right images, red: plasma cells). Cytogenetic analysis displayed an abnormal karyotype: 45,X,-X,t(11;14)(q13;q32)[4]/46,XX[16]. Overall findings were consistent with t(11;14) multiple myeloma (MM).

Dutcher bodies are now known as immunoglobulin inclusions overlying or invaginating into nuclei with no essential differences with Russell bodies.1 This case shows Dutcher and Russell bodies—uncommon morphological features most commonly seen in abnormal plasma cells. Literature search shows that Dutcher bodies in MM are highly associated with t(4;14) and IgA isotype, with the tendency of poor prognosis,2 whereas this case involved IgG-kappa isotype and t(11;14) translocation. The correlation of Dutcher and Russell bodies with both immunoglobulin heavy chain gene (IGH) rearrangement caused by chromosome 14 translocation calls for further study.

This work was supported by the Scientific and Technological Research Program of Chongqing Municipal Education Commission (KJQN202000443).

Not applicable (no ethical approval was necessary for this case).

Not applicable (no privacy of the patient is involved and no photographs of the patient or any parts will be published).

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一例 t(11;14)多发性骨髓瘤患者的 Dutcher 体和 Russell 体。
65岁女性,以背部疼痛为主。血清免疫固定电泳显示为免疫球蛋白G (IgG) kappa型单克隆蛋白。骨髓抽吸显示41%的异常浆细胞大小不同,细胞核规则或不规则,其中大部分细胞全部或部分覆盖细胞核(上图,黑色箭头所示的荷兰体,Wright染色,×100物镜)或/和细胞质内的罗素体(上图,红色箭头所示的罗素体)。骨髓活检在血红素和伊红染色中显示粉红色的Dutcher和Russell小体(左下图)。流式细胞术分析显示浆细胞为克隆(下图中、右图,红色为浆细胞)。细胞遗传学分析显示异常核型:45,X,-X,t(11;14)(q13;q32)[4]/46,XX[16]。总体结果与t(11;14)多发性骨髓瘤(MM)一致。荷兰小体现在被称为覆盖或内陷于细胞核内的免疫球蛋白包涵体,与罗素小体没有本质区别本例显示Dutcher和Russell小体,这些不常见的形态特征最常见于异常浆细胞。文献检索显示MM的荷兰体与t(4;14)和IgA同型高度相关,有预后不良的倾向2,而本病例涉及IgG-kappa同型和t(11;14)易位。Dutcher小体和Russell小体与14号染色体易位引起的免疫球蛋白重链基因重排的相关性有待进一步研究。重庆市教委科技攻关计划(KJQN202000443)资助。不适用(本案例不需要伦理批准)。不适用(不涉及病人的隐私,亦不会刊登病人的照片或任何部位)。
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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
期刊最新文献
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