Spontaneous Remission of Late Relapsing Membranous Nephropathy After Previous Immunosuppressant-Induced Remission: Case Report.

Case Reports in Nephrology Pub Date : 2026-04-12 eCollection Date: 2026-01-01 DOI:10.1155/crin/6703642
Yangming Cao
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Abstract

This is the first detailed report of spontaneous remission of late relapsing membranous nephropathy (MN) after previous immunosuppressant-induced remission. In March 2004, a 52-year-old Hispanic male presented with severe nephrotic syndrome with proteinuria of 13 g/24 h. The workup for infectious and autoimmune diseases was unrevealing. Renal biopsy showed MN (Stage II). A CT scan showed no malignancy but left pulmonary embolism and left renal vein thrombosis. Anticoagulation was started for asymptomatic thromboembolism. He achieved sustained complete remission of nephrotic syndrome after a prolonged, complicated treatment course of multiple immunosuppressants (corticosteroids and mycophenolate mofetil for 1 year, followed by alternating monthly corticosteroids and chlorambucil for 6 months, and again corticosteroids and mycophenolate mofetil for 6 years). Then in July 2021 (now at the age of 69 years), he developed nephrotic syndrome again with proteinuria of 6 g/24 h. Serological work-up was all negative except for the elevated serum Antiphospholipase A2 receptor (PLA2R) antibody at 42 RU/mL (nl < 14). Renal biopsy in November 2021 showed again MN (Stage III to IV). Immunohistochemistry staining of the biopsy tissue for PLA2R1 antigen was positive. A decision was made to observe him instead of starting immunosuppressants. He was treated with diuretics and Lisinopril. Anti-PLA2R antibody steadily improved to normal range and the nephrotic syndrome gradually improved and finally resolved by August 2023. There was no recurrence of nephrotic syndrome up to the most recent visit in March 2026. A review of the literature shows that a repeat biopsy in patients already known to have MN (especially those PLA2R-mediated cases) with relapse of nephrosis and stable renal function may not be necessary. In routine practice, the watchful waiting strategy for relapse of MN is less often taken as it should be. Therefore, more patients with relapsing MN deserve an observation period before starting immunosuppressants. Hopefully, KDIGO guidelines can include this point for relapsing MN.

既往免疫抑制剂诱导缓解后晚期复发性膜性肾病的自发缓解:病例报告。
这是首次详细报道在免疫抑制剂诱导缓解后晚期复发性膜性肾病(MN)的自发缓解。2004年3月,一名52岁的西班牙裔男性出现严重肾病综合征,伴有蛋白尿13 g/24 h。传染病和自身免疫性疾病的检查结果没有透露。肾活检显示MN (II期)。CT扫描显示无恶性肿瘤,但左肺栓塞和左肾静脉血栓形成。无症状血栓栓塞开始抗凝治疗。经过长期复杂的多种免疫抑制剂治疗(糖皮质激素和霉酚酸酯治疗1年,随后每月交替使用糖皮质激素和氯霉素治疗6个月,然后再次使用糖皮质激素和霉酚酸酯治疗6年),患者的肾病综合征得到持续完全缓解。2021年7月(现年69岁)再次出现肾病综合征,蛋白尿6 g/24 h。血清学检查除血清抗磷脂酶A2受体(PLA2R)抗体升高42 RU/mL (nl)外均为阴性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Case Reports in Nephrology
Case Reports in Nephrology Medicine-Nephrology
CiteScore
1.70
自引率
0.00%
发文量
32
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