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Excellent outcome of tubulointerstitial nephritis and uveitis: case report and five-year follow-up.

Abstract
Acute tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare disease usually having a good prognosis. But the recurrence of uveitis and the chronic progression of kidney injury are still main problems. We report a 15-year-old girl with TINU who showed proteinuria, pathological renal change, multiple organ dysfunction, and immune disorders. After 2 months of 1 mg/kg/day corticosteroid therapy, 24-h urine protein, liver function tests, and creatine kinase returned to normal level. In spite of this, steroid was tapered off slowly and small dose of steroid maintenance therapy lasted for 1 year. Her kidney and ocular symptoms did not recur during 5 years of follow-up. We suggest low-dose steroid maintenance therapy to decrease the recurrence of the TINU syndrome.
AuthorsLetian Zhou, Ying Li, Fuyou Liu, Youming Peng, Yinghong Liu, Jun Li
JournalRenal failure (Ren Fail) Vol. 34 Issue 7 Pg. 934-6 ( 2012) ISSN: 1525-6049 [Electronic] England
PMID22681193 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Glucocorticoids
  • Prednisone
Topics
  • Adolescent
  • Female
  • Glucocorticoids (therapeutic use)
  • Humans
  • Nephritis, Interstitial (drug therapy)
  • Prednisone (therapeutic use)
  • Treatment Outcome
  • Uveitis (drug therapy)

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