We report here the clinical features and outcomes of two patients who prese
nted idiopathic tubulo-interstitial nephritis and uveitis syndrome (TINU sy
ndrome) with ocular disease following the onset of nephropathy. The initial
symptoms were renal impairment with asthenia, anorexia and weight loss. An
increase in urinary PB-microglobulin was noticed at the initial checkup in
both patients, Renal biopsies showed interstitial cellular infiltration wi
thout granulomas or tubular atrophy. No glomerular and vascular alterations
were seen and immunofluorescent staining was uniformly negative. Systemic
steroid therapy was given and renal function returned to normal within thre
e months. Anterior uveitis occurred in both patients eight months later and
responded well to local steroid therapy. Renal involvement in TINU syndrom
e mostly has a favorable outcome. Despite the possibility of spontaneous re
gression, systemic steroids may be beneficial in reducing the development o
f interstitial fibrosis.