A case of tubulointerstitial nephritis and uveitis syndrome complicated with Fanconi syndrome and literature review / 中华肾脏病杂志
Chinese Journal of Nephrology
; (12): 56-60, 2024.
Article
en Zh
| WPRIM
| ID: wpr-1029275
Biblioteca responsable:
WPRO
ABSTRACT
The clinical diagnosis of tubulointerstitial nephritis and uveitis (TINU) syndrome combined with Fanconi syndrome is relatively rare. The paper reports a 47-year-old female patient of TINU syndrome with hypokalemia, hypophosphatemia, hypouricemia and renal impairment as initial symptoms followed by uveitis. Serological tests showed that the patient also met the diagnostic criteria of Fanconi syndrome. Renal tissue pathology confirmed tubular interstitial injury, manifested as interstitial nephritis with acute tubular injury. Ophthalmic examination confirmed iritis in the right eye. After excluding other primary diseases, the patient was diagnosed as TINU syndrome with Fanconi syndrome. After glucocorticoid therapy, ocular symptoms, renal impairment and electrolyte disturbance were significantly improved.
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Índice:
WPRIM
Idioma:
Zh
Revista:
Chinese Journal of Nephrology
Año:
2024
Tipo del documento:
Article