异基因骨髓移植后儿童类固醇依赖性肾病综合征1例报告

Uzma Zahid, M. Mahmood
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引用次数: 0

摘要

肾病综合征是儿童常见病。大多数对大剂量类固醇有反应,有些需要保留类固醇的免疫抑制方案,如果对类固醇治疗有耐药性,则需要肾活检。然而,异基因骨髓移植后的儿童肾病综合征是罕见的。作者在此报告了一名患有β-地中海贫血的儿童,在异基因骨髓移植后出现肾病综合征,疑似移植物抗宿主病,难以治疗,多次住院,复发频繁,疗程延长。在过去的5年里,该疾病在低剂量强的松龙和霉酚酸酯为基础的维持免疫抑制治疗下一直处于缓解期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Steroid-Dependent Nephrotic Syndrome in a Child After an Allogeneic Bone Marrow Transplant: A Case Report
Nephrotic syndrome is a frequently encountered disease in children. It is mostly responsive to high-dose steroids, with some requiring steroid-sparing immunosuppressive regimens, or further, a renal biopsy if resistant to steroid therapy. However, nephrotic syndrome in children post-allogeneic bone marrow transplant is rarely encountered. The authors report here a child who developed nephrotic syndrome post-allogeneic bone marrow transplant for β-thalassaemia major, with the suspicion of graft-versus-host disease that was difficult-to-treat, who had frequent relapses with multiple hospital admissions, and prolonged treatment course. For the last 5 years, the disease has been in remission, on a low dose of prednisolone and mycophenolate mofetil-based maintenance immunosuppressive treatment.
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