El-Husseini Amr, Aycinena Juan-Carlos, George Bennet, Jennings Stuart, Cornea Virgilius, Sawaya B Peter
Clin Nephrol. 2015 Oct;84(4):231-5. doi: 10.5414/CN108508.
Fibrillary glomerulonephritis (FGN) is a rare disorder with poor renal prognosis. It is a heterogeneous disease associated with significant risk of end-stage renal disease (ESRD). Its etiology and pathogenesis have not been clearly identified. We report a case of a patient presenting with hypertensive crisis, nephrotic range proteinuria, and rapidly progressive glomerulonephritis (RPGN). The kidney biopsy demonstrates crescentic GN on light microscopy (LM) and strong pseudo-linear/globular glomerular basement membrane (GBM) staining for immunoglobulin G on immunofluorescence (IF), suggestive of anti-GBM disease. However, circulating anti-GBM antibodies were negative. Electron microscopy (EM) revealed fibrillary deposits in the GBM, confirming the diagnosis of FGN. Review of the literature revealed very few reported similar cases. It appears that severe hypertension and heavy proteinuria, while uncommon in anti-GBM disease, are consistent findings in RPGN form of FGN.
纤维性肾小球肾炎(FGN)是一种罕见疾病,肾脏预后较差。它是一种异质性疾病,与终末期肾病(ESRD)的重大风险相关。其病因和发病机制尚未明确。我们报告一例患者,表现为高血压危象、肾病范围蛋白尿和快速进展性肾小球肾炎(RPGN)。肾脏活检在光镜(LM)下显示新月体性肾小球肾炎,免疫荧光(IF)显示免疫球蛋白G在肾小球基底膜(GBM)上呈强伪线性/球状染色,提示抗GBM病。然而,循环抗GBM抗体为阴性。电子显微镜(EM)显示GBM中有纤维状沉积物,确诊为FGN。文献复习显示报道的类似病例极少。似乎严重高血压和大量蛋白尿在抗GBM病中虽不常见,但在FGN的RPGN形式中是一致的表现。