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

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-11-02 DOI:10.1093/ajcp/aqae109
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.

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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。
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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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