Clinical Features in Tubulointerstitial Nephritis and Uveitis (TINU) Syndrome

2005 ◽  
Vol 140 (4) ◽  
pp. 637-641 ◽  
Author(s):  
Chiho Goda ◽  
Satoshi Kotake ◽  
Akira Ichiishi ◽  
Kenichi Namba ◽  
Nobuyoshi Kitaichi ◽  
...  
Keyword(s):  
Clinical Features ◽  
Tubulointerstitial Nephritis ◽  
Tinu Syndrome

A rare case of tubulointerstitial nephritis and uveitis (TINU) syndrome: Answers

2020 ◽  
Vol 35 (12) ◽  
pp. 2269-2274
Author(s):  
Douglas J. Stewart ◽  
Thivya Sekar ◽  
Kjell Tullus
Keyword(s):  
Rare Case ◽  
Tubulointerstitial Nephritis ◽  
Tinu Syndrome

scholarly journals Tubulointerstitial nephritis and uveitis (TINU) syndrome and recent Streptococcus infection in a 9-year-old girl

2020 ◽  
Vol 13 (2) ◽  
pp. e232077
Author(s):  
Robert BR Moreton ◽  
Brian W Fleck ◽  
Joyce Davidson ◽  
David Hughes
Keyword(s):  
Renal Function ◽  
Tubulointerstitial Nephritis ◽  
Sudden Onset ◽  
Outpatient Clinics ◽  
Glucocorticoid Treatment ◽  
Tinu Syndrome ◽  
Preserve Renal Function ◽  
Systemic Glucocorticoid ◽  
Clinical Investigations ◽  
History Of

A 9-year-old girl presented to hospital with a 6-week history of non-specific constitutional symptoms and weight loss. She initially underwent extensive medical investigation without diagnosis being achieved. Although raised inflammatory markers and impaired renal function were noted during her initial admission to hospital, it was her subsequent presentation 2 weeks later with sudden-onset bilateral anterior uveitis that prompted a renal biopsy that indicated acute tubulointerstitial nephritis. A diagnosis of tubulointerstitial nephritis and uveitis (TINU) syndrome was made and systemic glucocorticoid treatment initiated to prevent visual loss and preserve renal function. She has subsequently been reviewed in multidisciplinary outpatient clinics and treated with a tapering regimen of immunosuppressive therapy. Her treatment has been complicated by the side effects of glucocorticoids and by persistent relapses in ocular disease and abnormalities on urinalysis. Recent clinical investigations indicate that her uveitis is controlled and that renal function remains well preserved.

Tubulointerstitial nephritis and uveitis (TINU) syndrome caused by the Chinese herb “Goreisan”

2009 ◽  
Vol 13 (1) ◽  
pp. 73-76 ◽  
Author(s):  
Hisa Suzuki ◽  
Katsunobu Yoshioka ◽  
Masato Miyano ◽  
Isseki Maeda ◽  
Keiko Yamagami ◽  
...  
Keyword(s):  
Tubulointerstitial Nephritis ◽  
Chinese Herb ◽  
Tinu Syndrome

Tubulointerstitial Nephritis and Uveitis (TINU) Syndrome: A Case Report

2016 ◽  
Vol 25 ◽  
Author(s):  
Şiyar Erdoğmuş ◽  
Serkan Aktürk ◽  
Zeynep Kendi Çelebi ◽  
Kenan Keven ◽  
Şule Şengül ◽  
...  
Keyword(s):  
Case Report ◽  
Tubulointerstitial Nephritis ◽  
Tinu Syndrome

scholarly journals A case of tubulointerstitial nephritis and uveitis syndrome after suspected drug-induced acute interstitial nephritis

2021 ◽  
Author(s):  
Yukiko Kitamura ◽  
shohei kuraoka ◽  
Koji Nagano ◽  
hiroshi tamura
Keyword(s):  
Interstitial Nephritis ◽  
Tubulointerstitial Nephritis ◽  
Late Onset ◽  
Acute Interstitial Nephritis ◽  
Suspected Drug ◽  
Drug Induced ◽  
Ophthalmic Examination ◽  
Tinu Syndrome ◽  
Eye Symptoms

Distinguishing between late-onset TINU syndrome and drug-induced AIN remains difficult given that patients with TINU syndrome may develop uveitis long after the onset of AIN. Therefore, ophthalmic examination is required not only upon diagnosis but also continuously or when eye symptoms, and relapse of urinary findings are observed.

Parenchymal Renal Disease

2014 ◽  
pp. 626-637
Author(s):  
Mariam P. Alexander ◽  
Ajay K. Singh
Keyword(s):  
Renal Disease ◽  
Vascular Disease ◽  
Kidney Function ◽  
Clinical Features ◽  
Tubulointerstitial Nephritis ◽  
Clinical Syndrome ◽  
White Cell ◽  
Red Cell

Parenchymal renal disease can be considered anatomically under the headings of glomerular, tubular, tubulointerstitial, and vascular disease. Most patients present with a clinical syndrome of nephron injury. The clinical features of parenchymal renal disease frequently depend on the component of the kidney that is affected—for example, glomerulonephritis presents with worsened kidney function, hypertension, hematuria, proteinuria, and red cell casts. Tubulointerstitial nephritis presents with azotemia, pyuria and/or white cell casts.

A boy with IgA nephropathy complicated by tubulointerstitial nephritis and uveitis (TINU) syndrome

2015 ◽  
Vol 83 (2015) (02) ◽  
pp. 117-120 ◽  
Author(s):  
Shinsuke Fujita ◽  
Keisuke Sugimoto ◽  
Akane Izu ◽  
Tsukasa Takemura
Keyword(s):  
Iga Nephropathy ◽  
Tubulointerstitial Nephritis ◽  
Tinu Syndrome
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