{"title":"多发性骨髓瘤伴有针状结晶包涵体。","authors":"Wei Cai, Jing Wu, Mi Jiang, Zesong Yang","doi":"10.1111/bjh.19788","DOIUrl":null,"url":null,"abstract":"<p>A 41-year-old female patient was admitted to our endocrinology department with the symptoms of worsening malaise, difficulty in walking and numbness in her limbs. Blood tests revealed a red blood cell count of 3.11 × 10<sup>12</sup>/L, haemoglobin level of 97 g/L, urinary Igκ at 1.11 g/L, Igλ at 0.05 g/L, resulting in a κ/λ ratio of 22.20. Additional findings included urinary beta-microglobulin levels exceeding 2500 μg/L, urinary immunoglobulin at 23 mg/L, urinary albumin levels above 50 mg/L and serum beta-microglobulin at 5.36 μg/L. Bone marrow aspiration showed that 9% of the total cells were plasma cells, with 7% containing acicular crystalline inclusion bodies. These plasma cells varied in size, exhibited abundant cytoplasm and displayed eccentrically located nuclei. Some cells were binucleated, with the cytoplasm containing varying numbers of acicular crystalline inclusion bodies (Wright staining, 100× objective; images, upper left, middle, and right panels). Flow cytometry analysis revealed that 3.61% of the aberrant monoclonal plasma cells expressed CD45, CD38, CD138, CD81, CD117, CD27 and CD28dim, with kappa light chain restriction (images, lower left, middle and right panels). Based on these findings, a diagnosis of multiple myeloma, kappa light chain type, was established. The presence of crystalline immunoglobulin inclusions in this case is an uncommon occurrence. The presence of crystalline inclusions of immunoglobulin in this case is a rare finding. Crystallisation is thought to occur on the surface of the rough endoplasmic reticulum, where the biochemical properties of the particular monoclonal protein produced in that case of myeloma favour its condensation into a crystal structure (Miyoshi I, Daibata M, Saito T, Ohtsuki Y, Taguchi H. Bence Jones myeloma cells with crystalline inclusions. Intern Med 2006;45(5):337–8).</p><p>This study is supported by the Scientific and Technological Research Program of Chongqing Municipal Education Commission (KJQN202000443).</p><p>Ethical review and approval were waived for this study due to the retrospective description of a few cases without identifiable patient data.</p><p>Consent for publication, both in print and electronically, has been obtained from the patient.</p>","PeriodicalId":135,"journal":{"name":"British Journal of Haematology","volume":"205 5","pages":"1668-1669"},"PeriodicalIF":5.1000,"publicationDate":"2024-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/bjh.19788","citationCount":"0","resultStr":"{\"title\":\"Multiple myeloma with acicular crystalline inclusion bodies\",\"authors\":\"Wei Cai, Jing Wu, Mi Jiang, Zesong Yang\",\"doi\":\"10.1111/bjh.19788\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A 41-year-old female patient was admitted to our endocrinology department with the symptoms of worsening malaise, difficulty in walking and numbness in her limbs. Blood tests revealed a red blood cell count of 3.11 × 10<sup>12</sup>/L, haemoglobin level of 97 g/L, urinary Igκ at 1.11 g/L, Igλ at 0.05 g/L, resulting in a κ/λ ratio of 22.20. Additional findings included urinary beta-microglobulin levels exceeding 2500 μg/L, urinary immunoglobulin at 23 mg/L, urinary albumin levels above 50 mg/L and serum beta-microglobulin at 5.36 μg/L. Bone marrow aspiration showed that 9% of the total cells were plasma cells, with 7% containing acicular crystalline inclusion bodies. These plasma cells varied in size, exhibited abundant cytoplasm and displayed eccentrically located nuclei. Some cells were binucleated, with the cytoplasm containing varying numbers of acicular crystalline inclusion bodies (Wright staining, 100× objective; images, upper left, middle, and right panels). Flow cytometry analysis revealed that 3.61% of the aberrant monoclonal plasma cells expressed CD45, CD38, CD138, CD81, CD117, CD27 and CD28dim, with kappa light chain restriction (images, lower left, middle and right panels). Based on these findings, a diagnosis of multiple myeloma, kappa light chain type, was established. The presence of crystalline immunoglobulin inclusions in this case is an uncommon occurrence. The presence of crystalline inclusions of immunoglobulin in this case is a rare finding. Crystallisation is thought to occur on the surface of the rough endoplasmic reticulum, where the biochemical properties of the particular monoclonal protein produced in that case of myeloma favour its condensation into a crystal structure (Miyoshi I, Daibata M, Saito T, Ohtsuki Y, Taguchi H. Bence Jones myeloma cells with crystalline inclusions. 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引用次数: 0
摘要
一名 41 岁的女性患者因乏力、行走困难和四肢麻木症状加重而入住我院内分泌科。血液化验显示红细胞计数为 3.11 × 1012/L,血红蛋白水平为 97 g/L,尿 Igκ 为 1.11 g/L,Igλ 为 0.05 g/L,κ/λ 比值为 22.20。其他检查结果包括尿液中的β-微球蛋白含量超过 2500 微克/升,尿液中的免疫球蛋白含量为 23 毫克/升,尿液中的白蛋白含量超过 50 毫克/升,血清中的β-微球蛋白含量为 5.36 微克/升。骨髓抽吸结果显示,9%的细胞为浆细胞,7%含有针状结晶包涵体。这些浆细胞大小不一,细胞质丰富,细胞核偏心。一些细胞呈双核,胞质中含有数量不等的针状结晶包涵体(赖特染色,100×物镜;图片,左上、中、右面板)。流式细胞术分析表明,3.61%的异常单克隆浆细胞表达 CD45、CD38、CD138、CD81、CD117、CD27 和 CD28dim,卡帕轻链受限(图片,左下、中、右图)。根据这些结果,多发性骨髓瘤(kappa 轻链型)的诊断成立。该病例中出现结晶性免疫球蛋白包涵体并不常见。该病例中出现免疫球蛋白结晶包涵体是罕见的发现。结晶被认为发生在粗面内质网表面,该骨髓瘤病例中产生的特定单克隆蛋白的生化特性有利于其凝结成晶体结构(Miyoshi I, Daibata M, Saito T, Ohtsuki Y, Taguchi H. Bence Jones myeloma cells with crystalline inclusions.本研究得到了重庆市教委科技研究项目(KJQN202000443)的支持。由于本研究是对少数病例的回顾性描述,没有可识别的患者数据,因此免于伦理审查和批准。
Multiple myeloma with acicular crystalline inclusion bodies
A 41-year-old female patient was admitted to our endocrinology department with the symptoms of worsening malaise, difficulty in walking and numbness in her limbs. Blood tests revealed a red blood cell count of 3.11 × 1012/L, haemoglobin level of 97 g/L, urinary Igκ at 1.11 g/L, Igλ at 0.05 g/L, resulting in a κ/λ ratio of 22.20. Additional findings included urinary beta-microglobulin levels exceeding 2500 μg/L, urinary immunoglobulin at 23 mg/L, urinary albumin levels above 50 mg/L and serum beta-microglobulin at 5.36 μg/L. Bone marrow aspiration showed that 9% of the total cells were plasma cells, with 7% containing acicular crystalline inclusion bodies. These plasma cells varied in size, exhibited abundant cytoplasm and displayed eccentrically located nuclei. Some cells were binucleated, with the cytoplasm containing varying numbers of acicular crystalline inclusion bodies (Wright staining, 100× objective; images, upper left, middle, and right panels). Flow cytometry analysis revealed that 3.61% of the aberrant monoclonal plasma cells expressed CD45, CD38, CD138, CD81, CD117, CD27 and CD28dim, with kappa light chain restriction (images, lower left, middle and right panels). Based on these findings, a diagnosis of multiple myeloma, kappa light chain type, was established. The presence of crystalline immunoglobulin inclusions in this case is an uncommon occurrence. The presence of crystalline inclusions of immunoglobulin in this case is a rare finding. Crystallisation is thought to occur on the surface of the rough endoplasmic reticulum, where the biochemical properties of the particular monoclonal protein produced in that case of myeloma favour its condensation into a crystal structure (Miyoshi I, Daibata M, Saito T, Ohtsuki Y, Taguchi H. Bence Jones myeloma cells with crystalline inclusions. Intern Med 2006;45(5):337–8).
This study is supported by the Scientific and Technological Research Program of Chongqing Municipal Education Commission (KJQN202000443).
Ethical review and approval were waived for this study due to the retrospective description of a few cases without identifiable patient data.
Consent for publication, both in print and electronically, has been obtained from the patient.
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.