Abstract
Nephrotic syndrome recurred in 16 patients who had been free of the disease of an interval of 4 to 25 years. Their initial illness began in childhood and responsed to adrenocorticosteroid therapy; in 10 patients it was associated with few changes on light microscopic examination of kidney biopsy specimens. The late recurrence also responded to steroids, and in only 1 patient did low grade proteinuria persist after treatment. Renal biopsy specimens taken from 8 patients during late recurrence showed minimal-change nephrotic syndrome in 7 and focal segmental glomerulosclerosis in 1. Renal function remained normal in all patients. The late recurrence of minimal-change nephrotic syndrome has most of the features of that syndrome seen in the more typical childhood age group and should be managed similarly.
Original language | English (US) |
---|---|
Pages (from-to) | 69-72 |
Number of pages | 4 |
Journal | Annals of internal medicine |
Volume | 100 |
Issue number | 1 |
DOIs | |
State | Published - 1984 |
ASJC Scopus subject areas
- Internal Medicine