ISSN 1006-298X      CN 32-1425/R

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肾脏病与透析肾移植杂志 ›› 2024, Vol. 33 ›› Issue (4): 382-387.DOI: 10.3969/j.issn.1006-298X.2024.04.017

• 肾活检 • 上一篇    下一篇

Alport综合征肾移植后新发非典型抗肾小球基膜肾炎

  

  • 出版日期:2024-08-28 发布日期:2024-08-30

Atypical anti-glomerular basement membrane disease after renal transplantation of Alport syndrome patient

  • Online:2024-08-28 Published:2024-08-30

摘要: 青年男性患者,自体肾活检诊断为Alport综合征,肾移植术后6年,病程中血清肌酐和蛋白尿反复增高,肾活检组织学为肾小球系膜增生性病变,IgG沿肾小球基膜(GBM)呈线性沉积,电镜下观察肾小球系膜区有电子致密物沉积。结合临床,考虑为移植肾非典型抗GBM肾炎,同时伴混合性排斥反应、免疫复合物相关肾小球病。


关键词: 肾移植, Alport综合征, 移植后非典型抗肾小球基膜肾炎, 免疫复合物相关肾小球病

Abstract: A 19-year-old male presented with repeated increases of blood creatinine and urine protein six years after renal transplantation due to Alport syndrome and CKD stage 5D. Renal biopsy revealed mesangial proliferative glomerulonephritis, and linear deposition of IgG along glomerular basement membrane(GBM), and electron dense deposits in mesangial region on electron microscopy. The final diagnosis was allograft post-transplant anti-GBM nephritis, along with mixed rejection and immune complex nephritis.


Key words: renal transplantation, Alport syndrome, post-transplant anti-glomerular basement membrane nephritis, immune complex nephritis