异基因造血细胞移植治疗骨髓增生异常综合征后继发移植物抗宿主病的微小变化疾病

IF 0.7 Q4 UROLOGY & NEPHROLOGY Case Reports in Nephrology and Dialysis Pub Date : 2022-03-14 DOI:10.1159/000522333
O. Elghawy, John S. Wang, Alexander C. Hafey, A. Renaghan, R. Whitehair, T. Kindwall‐Keller
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引用次数: 2

摘要

慢性移植物抗宿主病(cGVHD)是异基因造血细胞移植(HCT)受者非复发性死亡的主要原因。虽然目前的治疗标准是在肺部、肝脏和皮肤中积极检测cGVHD,但涉及肾脏的cGVHD是hct后肾功能障碍的一个未被认识和可能未被诊断的原因。肾病综合征(NS)是一种非常罕见的HCT并发症,被认为是cGVHD的肾小球表现。在此,我们报告2例可能继发于cGVHD的hct后微小变化疾病。在这两例中,NS的发病与钙调磷酸酶抑制剂的逐渐减少同时发生,并且1例患者先前被诊断为肺部cGVHD。一名患者单独使用皮质类固醇,另一名患者同时使用皮质类固醇和他克莫司。两例患者均获得了完全、持续的缓解。我们的病例说明了cGVHD与hct后NS之间的关系对患者护理的意义,包括获得肾脏活检以建立准确的组织病理学诊断和指导适当治疗的重要性。
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Minimal Change Disease Secondary to Graft-versus-Host Disease after Allogeneic Hematopoietic Cell Transplant for Myelodysplastic Syndrome
Chronic graft-versus-host disease (cGVHD) is a leading cause of non-relapse mortality in allogeneic hematopoietic cell transplant (HCT) recipients. While the current standard of care is proactive in detecting cGVHD in the lungs, liver, and skin, cGVHD involving kidneys is an underrecognized and likely underdiagnosed cause of post-HCT renal dysfunction. Nephrotic syndrome (NS) is a very rare complication of HCT that is postulated to be a glomerular manifestation of cGVHD. Herein, we report 2 cases of post-HCT minimal change disease likely secondary to cGVHD. In both cases, the onset of NS coincided with tapering of calcineurin inhibitors, and 1 patient had previously been diagnosed with cGVHD of the lungs. One patient was treated with corticosteroids alone and the other with a corticosteroids and tacrolimus. Complete, sustained remission was achieved in both cases. Our cases illustrate the implications of the association between cGVHD and post-HCT NS for patient care, including the importance of obtaining a renal biopsy to establish an accurate histopathological diagnosis and guide-appropriate treatment.
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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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