Anti-GBM Disease after Oxford-AstraZeneca ChAdOx1 nCoV-19 Vaccination: A Report of Two Cases.

IF 0.7 Q4 UROLOGY & NEPHROLOGY Case Reports in Nephrology and Dialysis Pub Date : 2022-11-22 eCollection Date: 2022-09-01 DOI:10.1159/000525737
Craig Peter Coorey, Elaine Phua, Angela Chou, Yvonne Shen, Amanda Mather
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引用次数: 2

Abstract

There have been reports of rare de novo glomerular diseases following vaccination for coronavirus disease 2019 (COVID-19). We report two cases of anti-glomerular basement membrane (GBM) disease in previously healthy females after Oxford-AstraZeneca COVID-19 vaccine (ChAdOx1 nCoV-19). The first case was a 69-year-old female who developed lethargy and anuria approximately 8 weeks after her first dose of Oxford-AstraZeneca COVID-19 vaccine. The second case was a 72-year-old female who developed malaise and diarrhoea approximately 3 weeks after her second dose of Oxford-AstraZeneca COVID-19 vaccine. Both cases had severe acute kidney injury, raised anti-GBM antibody titres, and renal biopsies consistent with anti-GBM disease. Both cases were commenced on haemodialysis and treated with high dose glucocorticoids, cyclophosphamide, and plasmapheresis. Neither patient had recovery of renal function, and both remain dialysis dependent. These cases add to the previously reported cases of anti-GBM disease after mRNA COVID-19 vaccination. As more COVID-19 vaccinations are administered worldwide, it would be important for clinicians to be aware of this possible association, and continued surveillance is warranted.

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牛津-阿斯利康ChAdOx1 nCoV-19疫苗接种后的抗gbm疾病:附2例报告
有报道称,在接种2019冠状病毒病(COVID-19)疫苗后出现罕见的新生肾小球疾病。我们报告两例健康女性在接种牛津-阿斯利康COVID-19疫苗(ChAdOx1 nCoV-19)后出现抗肾小球基底膜(GBM)疾病。第一个病例是一名69岁的女性,她在第一次接种牛津-阿斯利康COVID-19疫苗约8周后出现嗜睡和无尿。第二个病例是一名72岁的女性,她在接种第二剂牛津-阿斯利康COVID-19疫苗约3周后出现不适和腹泻。两例均有严重的急性肾损伤,抗gbm抗体滴度升高,肾活检符合抗gbm疾病。两例患者均开始血液透析,并给予高剂量糖皮质激素、环磷酰胺和血浆置换治疗。两名患者均未恢复肾功能,均依赖透析治疗。这些病例增加了先前报道的mRNA - COVID-19疫苗接种后抗gbm疾病病例。随着全球范围内接种的COVID-19疫苗越来越多,临床医生必须意识到这种可能的关联,并有必要继续进行监测。
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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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