肾移植受者移植后新生肾磷脂病:法布里病还是别的什么?

Clinical Nephrology. Case Studies Pub Date : 2020-05-29 eCollection Date: 2020-01-01 DOI:10.5414/CNCS110131
Muhammad Saad Naseer, Raj Chand, Stefano Coppola, Adrian Abreo, Mukesh Sharma, Neeraj Singh
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引用次数: 7

摘要

肾磷脂病是一种罕见的蛋白尿和肾功能障碍的原因。我们描述了一例肾移植受者,移植后10年出现血清肌酐缓慢升高、肾病范围蛋白尿和下肢水肿。移植肾活检诊断为肾磷脂病。患者既往无法布里病病史或当前症状或体征。血清α-半乳糖苷酶水平正常。病因被怀疑是由于长期使用舍曲林,一个先前报道的药物性肾磷脂病的原因。停用舍曲林,6个月随访时,蛋白尿下降,肾功能稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Post-transplant de-novo renal phospholipidosis in a kidney transplant recipient: Fabry disease or something else?

Post-transplant de-novo renal phospholipidosis in a kidney transplant recipient: Fabry disease or something else?

Post-transplant de-novo renal phospholipidosis in a kidney transplant recipient: Fabry disease or something else?

Renal phospholipidosis is a rare cause of proteinuria and kidney dysfunction. We describe a kidney transplant recipient who presented with slowly rising serum creatinine, nephrotic range proteinuria, and lower extremity edema 10 years post transplant. He was diagnosed with renal phospholipidosis on the transplant kidney biopsy. Patient did not have prior history or current symptoms or signs of Fabry disease. Serum α-galactosidase level was normal. The etiology was suspected to be due to chronic use of sertraline, a previously reported cause of drug-induced renal phospholipidosis. Sertraline was discontinued, and proteinuria declined with stabilization of kidney function at 6-months follow-up.

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