De novo Minimal Change Disease in an Adolescent after Pfizer-BioNTech COVID-19 Vaccination: A Case Report

IF 0.7 Q4 UROLOGY & NEPHROLOGY Case Reports in Nephrology and Dialysis Pub Date : 2022-03-21 DOI:10.1159/000521981
Eva Pella, P. Sarafidis, M. Alexandrou, M. Stangou, C. Nikolaidou, D. Kosmidis, A. Papagianni
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引用次数: 9

Abstract

This is the first report in an adolescent of minimal change disease (MCD) after the first injection of the BNT162b2 COVID-19 vaccine (Pfizer-BioNTech) with complete remission following steroid treatment. An 18-year-old white male with no prior medical history complained of gastrointestinal symptoms 11 days after his vaccination. Ascites and lower extremity edema were observed a few days later. He was admitted to a hospital as laboratory testing revealed proteinuria of 10.5 g/24 h, normal creatinine levels, and serum albumin of 1.8 g/dL, confirming the presence of nephrotic syndrome. Immunology and serology tests were unremarkable. A diagnostic kidney biopsy showed no significant glomerular or tubular abnormalities in light microscopy with negative immunofluorescence. Treatment with methylprednisolone 48 mg daily was initiated. A week after discharge, proteinuria declined to 1.2 g/24 h, and edema had disappeared, and 6 weeks later, complete remission was evident. As COVID-19 vaccination has been associated with the development of de novo and relapsing MCD, and this case provides additional support for this possible correlation.
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一名青少年在辉瑞- biontech COVID-19疫苗接种后出现新生最小变化疾病:一例报告
这是首例在首次注射BNT162b2 COVID-19疫苗(辉瑞- biontech)后发生微小变化病(MCD)的青少年患者在类固醇治疗后完全缓解的报告。一名无既往病史的18岁白人男性在接种疫苗后11天出现胃肠道症状。几天后观察到腹水和下肢水肿。实验室检查显示蛋白尿10.5 g/24 h,肌酐水平正常,血清白蛋白1.8 g/dL,确认肾病综合征存在。免疫学和血清学检查无显著差异。诊断性肾活检显示光镜下免疫荧光阴性无明显肾小球或肾小管异常。开始每日48毫克甲基强的松龙治疗。出院后1周,蛋白尿下降至1.2 g/24 h,水肿消失,6周后完全缓解。由于COVID-19疫苗接种与新发和复发性MCD的发展有关,该病例为这种可能的相关性提供了额外的支持。
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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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