Intracapillary monoclonal IgM deposits disease with massive pseudothrombi: A clinicopathologic study of 4 cases and literature review.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Lei Ma, Dandan Liang, Xinchen Yao, Xiaoqing Yang, Suhua Li, Yelixiati Adelibieke, Feng Xu, Shaoshan Liang, Dacheng Chen, Fan Yang, Xiaoyu Wang, Yujie Tang, Ruoyu Jia, Caihong Zeng
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Abstract

Objectives: Intracapillary monoclonal IgM deposits disease (ICMDD) has long been considered a hallmark of Waldenström macroglobulinemia (WM) nephropathy. Intracapillary immunoglobulin thrombi are the characteristic features of cryoglobulinemic glomerulonephritis. Here, we reported 4 cases of ICMDD with massive pseudothrombi but without WM or cryoglobulinemia.

Methods: We retrospectively analyzed the clinical and pathologic features of patients diagnosed with ICMDD with massive pseudothrombi.

Results: A total of 4 patients (2 men and 2 women) aged 62 to 73 years were enrolled in this study. Microscopic hematuria, edema, and renal insufficiency were present in all patients, along with low serum C3 and C4 in 2 patients. Hematologic examination showed abnormal serum free light chain ratios in all patients and high levels of serum IgM in 3 patients. IgM-κ monoclonal band was identified by serum immunofixation electrophoresis in 3 patients. One patient was diagnosed with small B-cell lymphoma by bone marrow aspiration. Renal biopsy specimen showed massive periodic acid-Schiff-positive hyaline thrombi in the glomerular capillary lumens and also less mesangial, subendothelial, and subepithelial deposits on light microscopy. Immunofluorescence indicated positive staining for IgM (++) and κ light chain staining in the glomerular capillary lumens, capillary walls, and mesangium in all patients. By electron microscopy, the glomerular capillary lumens were filled with homogeneous high-electron-dense deposits without substructure. Two patients were treated with prednisone combined with cyclophosphamide, and 2 received plasma cell-targeted chemotherapy. One patient achieved partial renal remission.

Conclusions: Intracapillary monoclonal IgM deposits disease is a rare disease and not always related to WM. Most patients have IgM monoclonal immunoglobulinemia; renal biopsy specimens mainly show a large number of pseudothrombi in the glomerular capillary lumens. Cyclophosphamide is effective in some patients.

伴有大量假血栓的毛细血管内单克隆 IgM 沉积病:4例临床病理学研究和文献综述。
目的:毛细血管内单克隆 IgM 沉积病(ICMDD)一直被认为是瓦尔登斯特伦巨球蛋白血症(WM)肾病的特征。毛细血管内免疫球蛋白血栓是冷球蛋白血症肾小球肾炎的特征。在此,我们报告了4例伴有大量假性血栓但无WM或冷球蛋白血症的ICMDD病例:我们回顾性分析了被诊断为伴有大量假血栓的 ICMDD 患者的临床和病理特征:本研究共纳入了 4 例患者(2 男 2 女),年龄在 62 至 73 岁之间。所有患者均出现镜下血尿、水肿和肾功能不全,其中 2 名患者血清 C3 和 C4 偏低。血液学检查显示,所有患者的血清游离轻链比率异常,3 名患者的血清 IgM 水平较高。3 名患者的血清免疫固定电泳发现了 IgM-κ 单克隆带。一名患者通过骨髓穿刺确诊为小 B 细胞淋巴瘤。肾活检标本显示,肾小球毛细血管管腔内有大量周期性酸性-Schiff阳性透明血栓,光镜下系膜、内皮下和上皮下沉积物也较少。免疫荧光显示,所有患者的肾小球毛细血管管腔、毛细血管壁和系膜中的 IgM(++)和κ轻链染色均呈阳性。通过电子显微镜观察,肾小球毛细血管管腔内充满了均质的高电子密度沉积物,没有亚结构。两名患者接受了泼尼松联合环磷酰胺治疗,两名患者接受了浆细胞靶向化疗。其中一名患者的肾病得到了部分缓解:毛细血管内单克隆IgM沉积症是一种罕见疾病,并不总是与WM有关。大多数患者有IgM单克隆免疫球蛋白血症;肾活检标本主要显示肾小球毛细血管管腔内有大量假血栓。环磷酰胺对部分患者有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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