Collagenofibrotic glomerulopathy: a systemic disease

Am J Kidney Dis. 1999 Jan;33(1):123-7. doi: 10.1016/s0272-6386(99)70267-2.

Abstract

Collagenofibrotic glomerulopathy is a recently discovered entity that is characterized by massive accumulation of spiraled and frayed collagen fibrils in mesangial and subendothelial areas, and elevated serum levels of procollagen III peptide. We report the autopsy of a patient who received continuous ambulatory peritoneal dialysis (CAPD) therapy for 7 years. Autopsy disclosed that massive accumulation of peculiar collagen fibers was found not only in the kidney, but also in many organs including spleen, liver, myocardium, and thyroid gland. Although the possibility remains that CAPD for 7 years might change or aggravate the deposition of abnormal collagen, the current case suggests a possibility that collagenofibrotic glomerulopathy is a systemic disorder with abnormal metabolism of type III collagen.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Autopsy
  • Biopsy
  • Chronic Disease
  • Collagen / metabolism*
  • Fatal Outcome
  • Fibrosis
  • Humans
  • Immunohistochemistry
  • Kidney Diseases / metabolism
  • Kidney Diseases / pathology*
  • Kidney Diseases / therapy
  • Kidney Glomerulus / metabolism
  • Kidney Glomerulus / pathology*
  • Male
  • Peritoneal Dialysis, Continuous Ambulatory

Substances

  • Collagen