Malignancy-Associated Membranous Nephropathy with Positive Anti-PLA2R Autoantibodies: Coincidence or Connection.

IF 0.7 Q4 UROLOGY & NEPHROLOGY Case Reports in Nephrology and Dialysis Pub Date : 2021-11-18 eCollection Date: 2021-09-01 DOI:10.1159/000520399
Lyle W Baker, Jaime Jimenez-Lopez, Xochiquetzal J Geiger, Nabeel Aslam
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引用次数: 4

Abstract

Membranous nephropathy (MN) is currently classified as either primary - often associated with positive anti-phospholipase-A2 receptor (PLA2R) autoantibodies - or as secondary - associated with malignancy, infection, medications, or autoimmune disease. We present a case of biopsy-proven MN with very high serum titer of anti-PLA2R autoantibodies in a patient with a synchronous diagnosis of poorly differentiated esophageal adenocarcinoma and renal cell carcinoma who presented with nephrotic syndrome. Based on the current classification, MN in the presence of active malignancy is diagnosed as secondary and unlikely to have positive anti-PLA2R autoantibodies. This raises several questions: whether this patient has secondary MN associated with malignancy and coincidentally discovered anti-PLA2R autoantibodies, primary MN due to anti-PLA2R autoantibodies with coincidentally discovered malignancy, or whether malignancy can induce the formation of anti-PLA2R autoantibodies that result in MN. This case report highlights the importance of age-appropriate cancer screening, even in patients with presumed primary MN and positive anti-PLA2R autoantibodies.

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恶性相关膜性肾病伴抗pla2r自身抗体阳性:巧合或联系。
膜性肾病(MN)目前分为原发性(通常与阳性抗磷脂酶a2受体(PLA2R)自身抗体相关)和继发性(与恶性肿瘤、感染、药物或自身免疫性疾病相关)。我们报告一例活检证实的MN具有非常高的血清抗pla2r自身抗体滴度,患者同时诊断为低分化食管腺癌和肾细胞癌,并表现为肾病综合征。根据目前的分类,伴有活动性恶性肿瘤的MN被诊断为继发性,不太可能有抗pla2r自身抗体阳性。这就提出了几个问题:该患者是否患有与恶性肿瘤相关的继发性MN并巧合发现了抗pla2r自身抗体,还是由于抗pla2r自身抗体导致的原发性MN并巧合发现了恶性肿瘤,或者恶性肿瘤是否可以诱导抗pla2r自身抗体的形成而导致MN。本病例报告强调了与年龄相适应的癌症筛查的重要性,即使在推定原发MN和抗pla2r自身抗体阳性的患者中也是如此。
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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
36
审稿时长
10 weeks
期刊介绍: This peer-reviewed online-only journal publishes original case reports covering the entire spectrum of nephrology and dialysis, including genetic susceptibility, clinical presentation, diagnosis, treatment or prevention, toxicities of therapy, critical care, supportive care, quality-of-life and survival issues. The journal will also accept case reports dealing with the use of novel technologies, both in the arena of diagnosis and treatment. Supplementary material is welcomed.
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