Fibronectin glomerulopathy in a 34-year-old man: a case report

Ultrastruct Pathol. 2010 Aug;34(4):240-2. doi: 10.3109/01913121003783209.

Abstract

Fibronectin glomerulopathy is an inherited non-immune-mediated glomerulopathy associated with the massive deposition of fibronectin. It presents with proteinuria, microscopic hematuria, and hypertension that lead to end-stage renal failure in the second to sixth decade of life. A 34-year-old male was referred with proteinuria (6 g/day), microscopic hematuria and hypertension (220/130 mmHg). Renal biopsy specimen showed massive deposits of fibronectin in the mesangium and subendothelial spaces. After 20 months of multidrug treatment his renal function is stable.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Fibronectins / metabolism*
  • Glomerular Mesangium / metabolism
  • Glomerular Mesangium / ultrastructure
  • Hematuria / drug therapy
  • Hematuria / genetics
  • Hematuria / pathology
  • Humans
  • Hypertension / drug therapy
  • Hypertension / genetics
  • Hypertension / pathology
  • Kidney Diseases / drug therapy
  • Kidney Diseases / genetics
  • Kidney Diseases / metabolism
  • Kidney Diseases / pathology*
  • Kidney Glomerulus / metabolism
  • Kidney Glomerulus / pathology*
  • Male
  • Microscopy, Electron, Transmission
  • Proteinuria / drug therapy
  • Proteinuria / genetics
  • Proteinuria / pathology
  • Treatment Outcome

Substances

  • Fibronectins