A Case of Nephrotic Syndrome Associated with Distal Type Tubular Acidosis, Nephrocalcinosis and Renal Osteodystrophy.
- Author:
Young Mo SOHN
1
;
Pyung Kil KIM
;
In Joon CHOI
;
Chang Yun PARK
Author Information
1. Department of Pediatrics, College of Medicine Yonsei University, Seoul, Korea.
- Publication Type:Original Article
- MeSH:
Acidosis*;
Acidosis, Renal Tubular;
Biopsy;
Child, Preschool;
Femur;
Humans;
Korea;
Male;
Mesangial Cells;
Nephrocalcinosis*;
Nephrotic Syndrome*;
Prednisone;
Rare Diseases;
Renal Osteodystrophy*;
Urinalysis
- From:Journal of the Korean Pediatric Society
1980;23(4):321-325
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
A non-familial type nephrotic syndrome associated with distal renal tubual acidosis, nephrocalcinosis and renal osteodystropy is a very rare disease. A 4 year old boy was treated with prednisone under the impression of minimal lesion nephrotid syndrome but the response was not excellent along with persistant microhematuria in his serial urinalysis. Percutaneous renal biopsy speciman revealed microcalcification around afferent arteriols and peritubular area along with mild mesangial cell proliferations. Futher studies disclosed osteodystrophic change of the femurs. Patient had a typical forms of distal type renal tubular acidosis which was confirmed by NH4Cl and NaHCO3 loading tests. This case is the first cases of non-familial type nephrotic syndrome associated with nephrocalcinosis, renal osteodystrophy and distal RTA in Korea.
