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Purpose: Tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare autoimmune disorder characterized by concurrent renal and ocular inflammation. Auditory features resembling Cogan's syndrome have been reported in TINU, though the nature of this overlap remains poorly understood. Here, we report a pediatric case of atypical Cogan syndrome to contribute to the growing literature on this unusual clinical association.
Materials And Methods: Description of a case report and overview of the current literature.
Results: 12-year-old female with TINU syndrome characterized by bilateral anterior uveitis and renal dysfunction, later suffered from a sudden-onset unilateral sensorineural hearing loss (SNHL). After a course of immunosuppressive therapy, only auditory symptoms persisted. This case highlights the phenotypic variability of TINU syndrome with atypical Cogan features, emphasizing the need for early recognition, multidisciplinary management, and further research to elucidate shared pathophysiological mechanisms.
Conclusions: Auditory manifestations in TINU syndrome reveal phenotypic diversity and possible overlap with Cogan syndrome, requiring early diagnosis and multidisciplinary management.
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http://dx.doi.org/10.1080/09273948.2025.2548949 | DOI Listing |
Cureus
August 2025
General Internal Medicine and Nephrology, Robert Bosch Krankenhaus, Stuttgart, DEU.
Tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare autoimmune condition primarily affecting adolescents. Diagnosis is frequently delayed due to the nonspecific and temporally dissociated presentation of renal and ocular symptoms. We report the case of a 15-year-old girl who presented to her general practitioner with fatigue, polyuria, and recent weight loss.
View Article and Find Full Text PDFOcul Immunol Inflamm
August 2025
Department of Paediatric Rheumatology, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Purpose: Tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare autoimmune disorder characterized by concurrent renal and ocular inflammation. Auditory features resembling Cogan's syndrome have been reported in TINU, though the nature of this overlap remains poorly understood. Here, we report a pediatric case of atypical Cogan syndrome to contribute to the growing literature on this unusual clinical association.
View Article and Find Full Text PDFJ Ophthalmic Inflamm Infect
July 2025
University Hospital Waterford, Waterford, Ireland.
Purpose: Tubulointerstitial nephritis and uveitis (TINU) syndrome, characterised by the co-occurrence of tubulointerstitial nephritis and uveitis in the absence of other systemic diseases, presents a diagnostic challenge due to its non-specific symptoms. This case series aims to shed light on TINU syndrome's clinical features, underlying causes, and management strategies. The prevalence of TINU syndrome is relatively low with estimates of 3.
View Article and Find Full Text PDFBMC Geriatr
July 2025
Department of Traditional Chinese Medicine, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, China.
Background: Tubulointerstitial nephritis and uveitis (TINU) syndrome is prevalent among adolescent females and less prevalent among the older people. Additionally, although both disorders are linked to immune modulation, clinical instances of simultaneous diagnosis of TINU syndrome and monoclonal gammopathies (MG) are exceedingly rare. In this case report, we present a rare concurrence of monoclonal gammopathies in an older adult with TINU syndrome.
View Article and Find Full Text PDFBMJ Case Rep
May 2025
School of Medicine, Griffith University, Brisbane, Queensland, Australia.
A woman in her 50s contracted COVID-19 and initially presented a few weeks afterwards with left eye pain and redness. She was diagnosed with uveitis and treated with glucocorticoid eye drops. Renal impairment was found on laboratory investigations performed following the diagnosis of uveitis, and urine testing showed proteinuria.
View Article and Find Full Text PDF