Suppr超能文献

抗中性粒细胞胞质抗体相关性血管炎合并多发性骨髓瘤患者同时存在髓过氧化物酶抗体和抗肾小球基底膜抗体双阳性:病例报告。

Coexistence of double seropositivity for MPO antibody and anti-GBM antibody in ANCA-associated vasculitis concurrent with multiple myeloma: A case report.

机构信息

Division of Nephrology, Department of Internal Medicine, Keimyung University School of Medicine, Keimyung University Kidney Institute, Daegu, Republic of Korea.

Division of Hematology-Oncology, Department of Internal Medicine, Keimyung University School of Medicine, Daegu, Republic of Korea.

出版信息

Medicine (Baltimore). 2024 Jul 26;103(30):e39021. doi: 10.1097/MD.0000000000039021.

Abstract

RATIONALE

Immune-mediated vasculitis with 2 or more autoantibodies, for example, anti-proteinase-3, combined with anti-myeloperoxidase (MPO) or anti-glomerular basement membrane (GBM) antibodies, is extremely unusual. Furthermore, the coexistence of autoimmune vasculitis and hematological malignancies is uncommon. Herein, we describe a case of double-seropositive anti-neutrophil cytoplasmic antibody (ANCA) vasculitis with multiple myeloma.

PATIENT CONCERNS

A 79-year-old Asian man presented with persistent leg edema and kidney dysfunction. His kidney function rapidly decreased, and serologic test results showed higher titers of the anti-MPO antibody (54.7 IU/mL) and anti-GBM antibodies (>200 IU/mL). Additionally, the clinical features showed the possibility of monoclonal gammopathy with anemia and hyperglobulinemia. We performed kidney and bone marrow biopsy. Serum protein electrophoresis and immunofixation revealed no significant differences, but the results of the bone marrow smear were compatible with those of myeloma with 15% plasmacytosis. However, kidney biopsy showed diffuse crescentic glomerulonephritis without deposition of the immune complex or kappa/lambda chain.

DIAGNOSES AND INTERVENTIONS

Finally, the patient was diagnosed with double-seropositive ANCA-associated glomerulonephritis and multiple myeloma. Given the patient's performance status, we initiated low-dose steroid pulse therapy, followed by conservative management.

OUTCOMES

While the pulmonary lesions showed improvement, the kidney function did not regain its previous state, prompting the initiation of kidney replacement therapy by hemodialysis. There has been a decrease in the levels of anti-GBM and anti-MPO antibodies since the initial diagnosis.

LESSONS

This case elucidates the complex interplay between ANCA-associated glomerulonephritis and hematologic malignancy and emphasizes the need for a nuanced treatment strategy considering its multifaceted clinical presentation.

摘要

背景

同时存在两种或以上自身抗体,如抗蛋白酶 3 抗体,以及抗髓过氧化物酶(MPO)或抗肾小球基底膜(GBM)抗体的免疫介导性血管炎极其罕见。此外,自身免疫性血管炎与血液系统恶性肿瘤同时存在也并不常见。在此,我们报告一例双重血清阳性抗中性粒细胞胞质抗体(ANCA)血管炎合并多发性骨髓瘤病例。

病例描述

一名 79 岁亚裔男性,以持续性腿部水肿和肾功能不全为主要表现。其肾功能迅速恶化,血清学检测结果显示抗 MPO 抗体(54.7 IU/mL)和抗 GBM 抗体滴度升高(>200 IU/mL)。此外,临床特征提示可能存在单克隆丙种球蛋白病合并贫血和高球蛋白血症。我们进行了肾脏和骨髓活检。血清蛋白电泳和免疫固定电泳无明显差异,但骨髓涂片结果符合浆细胞增多症,浆细胞占比 15%。然而,肾脏活检显示弥漫性新月体性肾小球肾炎,无免疫复合物或κ/λ 轻链沉积。

诊断与干预

最终,该患者被诊断为双重血清阳性 ANCA 相关肾小球肾炎合并多发性骨髓瘤。鉴于患者的一般状况,我们给予低剂量激素脉冲治疗,随后采取保守治疗。

治疗结果

肺部病变有所改善,但肾功能未能恢复到之前的状态,故开始进行血液透析以替代肾脏功能。自最初诊断以来,抗 GBM 和抗 MPO 抗体的水平有所下降。

经验教训

本病例阐明了 ANCA 相关肾小球肾炎与血液系统恶性肿瘤之间的复杂相互作用,并强调了需要根据其多方面的临床表现制定细致的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b71/11272363/8e49a083c697/medi-103-e39021-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验