医学
肾炎
免疫学
抗体
病理
肌酐
接种疫苗
间质性肾炎
肾脏疾病
等离子体电池
肾小球肾炎
抗原
病毒
活检
肾活检
快速进行性肾小球肾炎
肾小球疾病
单克隆抗体
疾病
自身免疫性疾病
间质性肺病
免疫球蛋白G
肾
单克隆
肾病
免疫球蛋白M
内科学
精神障碍
作者
Liqin Zhang,Wenjuan Wang,Rong Xue,Jian Zhang,Yanan Hao,Xiaoli Li
摘要
Atypical anti-glomerular basement membrane (GBM) nephritis is a rare autoimmune disease characterized by the linear deposition of immunoglobulin G (IgG) detected in the GBM without circulating anti-GBM antibodies or lung involvement. Atypical anti-GBM disease is distinguished from typical anti-GBM disease in both clinical and pathological features. Herein, we report 2 patients who developed mild proteinuria, hematuria, and elevated serum creatinine levels following coronavirus disease 2019 (COVID-19) vaccination. Renal biopsy found bright linear IgG deposition along the GBM, but anti-GBM antibodies were seronegative. Atypical anti-GBM nephritis was determined. The female patient improved with the treatment of valsartan. For the male patient, serum creatinine levels significantly decreased through two plasma exchange sessions, cyclophosphamide, and glucocorticoid. Atypical and typical anti-GBM nephritis are different clinical entities. They target different antigen epitopes and, therefore, atypical anti-GBM disease is not the early stage of typical anti-GBM disease. In atypical anti-GBM nephritis, monoclonal IgG deposition in the glomeruli is not equal to plasma cell dyscrasias but still needs close monitoring for hematologic diseases. The relationship between the disease and COVID-19 vaccination is uncertain and needs further exploration.
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