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Spontaneous Remission of De Novo Membranous Nephropathy in Post-Allogeneic Hematopoietic Stem Cell Transplantation Patients: A Report of Two Cases.

Clinical Nephrology(2024)

Mem Sloan Kettering Canc Ctr | St Josephs Hosp | Weill Cornell Med Coll

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Abstract
Membranous nephropathy (MN) is one of the most common de novo glomerular diseases developing in patients after allogeneic hematopoietic stem cell transplantation (HSCT). Most authors have used immunosuppression for its treatment to target the underlying immune-mediated processes, akin to graft-versus-host disease, but the optimal management is currently unclear. Limited reports in the literature described the use of a conservative approach with success, particularly in cases with lower risks of progression, such as non-nephrotic-range proteinuria or early reduction of proteinuria by 6 months. We report two cases of post-HSCT MN with moderate risk features, namely prolonged durations of nephrotic-range proteinuria, that spontaneously resolved with conservative treatment. Patient 1 was of advanced age and in an immunocompromised state, while patient 2 was in need of a greater graft-versus-disease effect from the donor's immune system, which necessitated a balance between the risk of immunosuppression and the risk of progressive kidney function loss. These cases demonstrated that conservative treatment can be a reasonable approach in selected patients with post-HSCT MN, including those with moderate risk.
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hematopoietic stem cell,transplantation,bone marrow transplantation,membranous nephropathy,graft-versus-host disease
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要点】:本文报道了两例在异基因造血干细胞移植后发生膜性肾病(MN)的患者,通过保守治疗实现了自发缓解,提出了在特定患者群体中保守治疗的有效性。

方法】:通过回顾性病例分析,研究了膜性肾病在异基因造血干细胞移植后的自发缓解情况。

实验】:研究了两位患者,一位年龄较大且免疫系统受损,另一位需要更强的移植物抗病效果,采用保守治疗,数据集为病例报告中的患者信息,结果显示两位患者的肾病均得到自发缓解。