A case of crescentic glomerulonephritis associated with relapsing polychondritis
Relapsing polychondritis (RP) is a rare autoimmune disease, characterized by recurrent inflammatory episodes affecting various carttilageus structures. Renal involvement in RP is unusual. Our case was a 42-year old woman presented with nephretic syndrome. Diagnosis of RP was made because of recurren...
Saved in:
Published in | Journal of renal injury prevention Vol. 8; no. 1; pp. 62 - 64 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
01.03.2019
|
Online Access | Get full text |
Cover
Loading…
Summary: | Relapsing polychondritis (RP) is a rare autoimmune disease, characterized by recurrent inflammatory episodes affecting various carttilageus structures. Renal involvement in RP is unusual. Our case was a 42-year old woman presented with nephretic syndrome. Diagnosis of RP was made because of recurrent chondritis of both auricles, chondritis of costovertebral joints, non-erosive inflammatory arthritis of knees, and inflammation of ocular structures. Renal biopsy findings revealed diffuse crescentic and sclerotic glomerulonephritis, pauciimmune type. The diagnosis of RP may be missed when the destructive cartilage feature is not apparent or rare presentation of disease such as ocular or renal involvement preceded other manifestations. In this case we found that the irregular prednisolone use may prevent destructive cartilage damage but not renal failure of patient. We concluded that the association of crescentic glomerulonephritis in a patient with RP was assumed to be a rare manifestation of this disease. |
---|---|
ISSN: | 2345-2781 2345-2781 |
DOI: | 10.15171/jrip.2019.12 |