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多靶点治疗诱导 IgG4 相关膜性肾病缓解。

Remission Induction of IgG4-related Membranous Nephropathy with Multitarget Therapy.

机构信息

Department of Hypertension and Nephrology, NTT Medical Center Tokyo, Japan.

Department of Diagnostic Pathology, NTT Medical Center Tokyo, Japan.

出版信息

Intern Med. 2023 Nov 1;62(21):3175-3181. doi: 10.2169/internalmedicine.1023-22. Epub 2023 Mar 15.

Abstract

IgG4-related membranous nephropathy (MN) is often refractory to glucocorticoid (GC) therapy, and treatment remains unclear. We herein report a 67-year-old Japanese man with IgG4-related MN and tubulointerstitial nephritis. A post-gastroscopy antibody test revealed Helicobacter pylori infection. After eradication, his proteinuria decreased indefinitely. We started prednisolone (30 mg/day), long-term GCs, and immunosuppressant therapy. However, remission proved challenging to achieve, with persistent proteinuria present at 1.0-2.0 g/gCr. We performed multitarget therapy for refractory IgG4-related MN, achieving proteinuria remission (<0.3 g/gCr). Multitarget therapy with low-dose GCs can resolve refractory IgG4-related MN through remission induction of proteinuria and minimize the risks associated with GC therapy.

摘要

IgG4 相关膜性肾病 (MN) 常对糖皮质激素 (GC) 治疗产生抵抗,治疗仍不明确。我们在此报告一例 IgG4 相关 MN 伴肾小管间质性肾炎的 67 岁日本男性。胃镜检查后抗体检测提示幽门螺杆菌感染。除菌后,患者蛋白尿持续减少。我们开始使用泼尼松龙(30mg/天)、长期 GC 和免疫抑制剂治疗。然而,尽管我们尝试了多种治疗方案,患者仍难以缓解,蛋白尿持续存在于 1.0-2.0g/gCr。我们对该例难治性 IgG4 相关 MN 患者进行了多靶点治疗,实现了蛋白尿缓解(<0.3g/gCr)。对于难治性 IgG4 相关 MN,小剂量 GC 的多靶点治疗可通过诱导蛋白尿缓解来解决,并最大程度降低 GC 治疗的相关风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d60/10686725/2e7a1bcf1376/1349-7235-62-3175-g001.jpg

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