Abstract

BackgroundAn increasing number of case reports suggest that acquired renal Fanconi syndrome may be associated with prolonged use of adefovir against hepatitis B virus. Renal Fanconi syndrome is an uncommon disease, and its complication with nephrolithiasis is quite rare. Herein, we report a rare coexistence of nephrolithiasis and acquired renal Fanconi syndrome in a chronic hepatitis B-positive patient with prolonged adefovir therapy.Case presentationThe patient presented with osteomalacia and nephrolithiasis. Consequently, extracorporeal shock-wave lithotripsy and left double-J ureteral stent insertion were considered for obstructive nephropathy, which was caused by nephrolithiasis. However, osteomalacia had been misdiagnosed as osteoporosis before admission to our hospital. On admission, a complexity of multiple fractures, hypophosphataemia, glycosuria without hyperglycaemia and non–anion-gap metabolic acidosis indicated a diagnosis of acquired renal Fanconi syndrome induced by adefovir. After switching from adefovir to entecavir, the patient’s symptoms and laboratory findings improved significantly.ConclusionsThe mechanism responsible for nephrolithiasis in renal Fanconi syndrome is still unclear. We recommend regularly monitoring renal function and serum calcium and serum phosphate to prevent renal Fanconi syndrome during the prolonged use of adefovir for hepatitis B virus.

Highlights

  • An increasing number of case reports suggest that acquired renal Fanconi syndrome may be associated with prolonged use of adefovir against hepatitis B virus

  • Adefovir dipivoxil-induced acute tubular necrosis and Fanconi syndrome have been well known to occur at a dose of 60 mg/d or 120 mg/d for human immunodeficiency virus (HIV) [1, 2]

  • We describe for the first time a case of nephrolithiasis and osteomalacia associated with adefovir-induced renal Fanconi syndrome

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Summary

Conclusions

It remains a challenge for scientists and clinicians to understand the relationships among adefovir, Fanconi syndrome and nephrolithiasis. Until the mechanisms responsible for adefovir nephrotoxicity are clarified, we recommend regularly monitoring renal function, serum calcium and serum phosphate to prevent renal Fanconi syndrome during the prolonged use of adefovir for HBV for patients with high-risk factors for renal impairment, such as low BMI, old age and decreased GFR. Abbreviations 18-FDG-PET/CT: 18F–fluorodeoxyglucose positron emission tomography computed tomography; 25(OH)D3: 25-hydroxyvitamin D3; 99mTcDTPA: technetium-99 m diethylene triamine penta-acetic acid; AB: actual bicarbonate; ALP: alkaline phosphatase; BMI: body mass index; DXA: dual energy X-ray absorptiometry; FBG: fasting blood-glucose; HBV: hepatitis B virus; HIV: human immunodeficiency virus; mg/d: milligram/day; NA: not available; NaPi-IIa: Renal sodium-inorganic phosphate cotransporter NaPi-IIa; PTH: parathyroid hormone; β2-MG: β2-microglobulin

Background
Discussion

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