Legionella pneumonia complicated with acquired fanconi syndrome

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Abstract

Legionella pneumonia is occasionally accompanied by renal complications; however, the cause of this remains unknown. We herein report a 70-year-old Japanese man with Legionella pneumonia who presented with hyponatremia, hypophosphatemia, and hypouricemia. The levels of urinary β2-microglobulin and N-acetyl-β-D-glucosaminidase were remarkably high, indicating severe renal tubular damage. The presence of glycosuria and aminoaciduria as well as increased fractional excretion of uric acid and decreased tubular re-absorption of phosphate indicated that the patient’s condition was complicated with Fanconi syndrome. After antimicrobial therapy, the electrolyte abnormalities and renal tubular damage were completely resolved.

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Koda, R., Itoh, R., Tsuchida, M., Ohashi, K., Iino, N., Takada, T., & Narita, I. (2018). Legionella pneumonia complicated with acquired fanconi syndrome. Internal Medicine, 57(20), 2975–2980. https://doi.org/10.2169/internalmedicine.0942-18

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