ArticleClinical and experimental nephrology2006
Tubulointerstitial nephritis and uveitis syndrome associated with hyperthyroidism.
Article in Clinical and experimental nephrology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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8 citing papers in PubMed, 26 citations in OpenAlex.
- Thyroid hormone signaling in ocular development and diseases.Biological research · 2025Review
- Association Between Thyroid Disease and Uveitis: Results From the Pacific Ocular Inflammation Study.JAMA ophthalmology · 2017Article
- Thyroid dysfunction and kidney disease: An update.Reviews in endocrine & metabolic disorders · 2017Review
- Tubulointerstitial nephritis with uveitis in Chinese adults.Clinical journal of the American Society of Nephrology : CJASN · 2014Article
- [Tubulointerstitial nephritis with uveitis (TINU) syndrome. A relatively rare rheumatological differential diagnosis with unexplained uveitis].Zeitschrift fur Rheumatologie · 2013Article
- Interactions between thyroid disorders and kidney disease.Indian journal of endocrinology and metabolism · 2012Article
- Tubulointerstitial nephritis and uveitis syndrome with transient hyperthyroidism in an elderly patient.Clinical and experimental nephrology · 2011Article
- Tubulointerstitial nephritis and uveitis (TINU) syndrome: epidemiology, diagnosis and management.NDT plus · 2008Article
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8 authors at 3 institutions in 1 country.
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Abstract
We report a 17-year-old male patient with tubulointerstitial nephritis and uveitis (TINU) associated with hyperthyroidism. He presented with a 2-month history of fatigue, loss of appetite, low-grade fever, and a 12-kg weight loss when he was admitted to our hospital. He had iritis, which was complicated by fibrin in the anterior chamber, diagnosed by slit-lamp examination. On laboratory examinations, deteriorated renal function (blood urea nitrogen level was 25.9 mg/dl and creatinine level was 2.82 mg/dl) and elevated urinary levels of N-acetyl-beta-D-glucosaminidase (33.1 U/l) and beta2-microglobulin (78,600 microg/l) were observed. Serum thyroid-stimulating hormone (TSH) was undetectable, at less than 0.01 microIU/ml, and free triiodothyronine and free thyroxine were elevated, up to 5.23 pg/ml and 2.85 ng/dl, respectively. The titers of antithyroglobulin and antithyroid microsomal and TSH-receptor antibodies were not elevated. Abdominal and thyroidal ultrasonography showed evident bilateral enlargement of the kidneys and diffuse enlargement of the thyroid gland. Iodine-123 scintigraphy showed low uptake in the thyroid gland. The biopsied renal specimen showed mild edema and severe diffuse infiltration of mononuclear cells and few eosinophils in the interstitium, without any glomerular or vascular abnormalities. Based on the clinical features and pathological findings, a diagnosis of TINU syndrome with associated hyperthyroidism was made. Treatment was started with 30 mg/day of prednisolone. The iritis disappeared, and the patient's clinical status improved remarkably. This case suggests the possibility of thyroid dysfunction in some patients with TINU syndrome, and we believe thyroid function should be measured in all TINU patients. Moreover, histopathological diagnosis of the thyroid glands before treatment is necessary for TINU patients with thyroid dysfunction.
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