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