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DOI 10.1093/ajcp/aqae109

Медицинская библиотека · American journal of clinical pathology · 2025

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

Ma Lei, Liang Dandan, Yao Xinchen, Yang Xiaoqing, Li Suhua, Adelibieke Yelixiati, Xu Feng, Liang Shaoshan, Chen Dacheng, Yang Fan, Wang Xiaoyu, Tang Yujie, Jia Ruoyu, Zeng Caihong

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Аннотация

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.

Для цитирования: Ma Lei, Liang Dandan, Yao Xinchen, Yang Xiaoqing, Li Suhua, Adelibieke Yelixiati, Xu Feng, Liang Shaoshan, Chen Dacheng, Yang Fan, Wang Xiaoyu, Tang Yujie, Jia Ruoyu, Zeng Caihong. Intracapillary monoclonal IgM deposits disease with massive pseudothrombi: A clinicopathologic study of 4 cases and literature review.. American journal of clinical pathology. 2025. DOI: 10.1093/ajcp/aqae109.

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