Kidney Res Clin Pract.  2012 Dec;31(4):253-256.

A case of membranous nephropathy associated with relapsing polychondritis

Affiliations
  • 1Department of Internal Medicine, Dankook University Hospital, Anseo-dong, Cheonan, Chungcheongnam Do, Korea. nephrologylek@hanmail.net

Abstract

Relapsing polychondritis (RP) is a rare, chronic, and potentially fatal multisystemic inflammatory disorder targeting cartilaginous structures. This disorder is frequently associated with rheumatoid arthritis, systemic vasculitis, connective tissue diseases, and hematologic disorders, but renal involvement is unusual. In the literature, associated renal pathology includes mesangial expansion, IgA nephropathy, tubulointerstitial nephritis, and segmental necrotizing crescentic glomerulonephritis. We report a case of a 49-year-old male found to have RP and nephrotic syndrome, with confirmed membranous nephropathy on kidney biopsy. He responded well to corticosteroids and cyclosporine. This is the first case of renal associated RP confirmed by renal biopsy in Korea. Membranous nephropathy associated with RP has never before been reported.

Keyword

Kidney; Membranous nephropathy; Nephrotic syndrome; Relapsing polychondritis

MeSH Terms

Adrenal Cortex Hormones
Arthritis, Rheumatoid
Biopsy
Connective Tissue Diseases
Cyclosporine
Glomerulonephritis
Glomerulonephritis, IGA
Glomerulonephritis, Membranous
Humans
Kidney
Korea
Male
Nephritis, Interstitial
Nephrotic Syndrome
Polychondritis, Relapsing
Systemic Vasculitis
Adrenal Cortex Hormones
Cyclosporine
Full Text Links
  • KRCP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr