Clinical features suggesting renal hypouricemia as the cause of acute kidney injury: a case report and review of the literature

被引:4
|
作者
Mazzierli, Tommaso [1 ]
Cirillo, Luigi [1 ,2 ]
Palazzo, Viviana [3 ]
Ravaglia, Fiammetta [4 ]
Becherucci, Francesca [1 ,2 ]
机构
[1] Univ Florence, Dept Biomed Expt & Clin Sci Mario Serio, Florence, Italy
[2] Meyer Univ Hosp, Nephrol & Dialysis Unit, Florence, Italy
[3] Meyer Univ Hosp, Med Genet Unit, Florence, Italy
[4] Santo Stefano Hosp, Nephrol & Dialysis Unit, Prato, Italy
关键词
Renal hypouricemia; AKI; EIAKI; Uric acid; MUTATION;
D O I
10.1007/s40620-022-01494-8
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Hypouricemia is defined as a level of serum uric acid below 2 mg/dl. Renal hypouricemia is related to genetic defects of the uric acid tubular transporters urate transporter 1 and glucose transporter 9. Patients with renal hypouricemia can be completely asymptomatic or can develop uric acid kidney stones or acute kidney injury, particularly after exercise. Renal hypouricemia is especially challenging to diagnose in patients with acute kidney injury, due to the nonspecific clinical, hematochemical and histological features. No common features are reported in the literature that could help clinicians identify renal hypouricemia-acute kidney injury. Currently available guidelines on diagnosis and management of renal hypouricemia provide limited support in defining clues for the differential diagnosis of renal hypouricemia, which is usually suspected when hypouricemia is found in asymptomatic patients. In this paper we report a case of renal hypouricemia-acute kidney injury developing after exercise. We carried out a review of the literature spanning from the first clinical description of renal hypouricemia in 1974 until 2022. We selected a series of clinical features suggesting a diagnosis of renal hypouricemia-acute kidney injury. This may help clinicians to suspect renal hypouricemia in patients with acute kidney injury and to avoid invasive, costly and inconclusive exams such as renal biopsy. Considering the excellent outcome of the patients reported in the literature, we suggest a "wait-and-see" approach with supportive therapy and confirmation of the disease via genetic testing.
引用
收藏
页码:651 / 657
页数:7
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