Two cases of nephrotic syndrome (NS)-induced acute kidney injury (AKI) associated with renal hypouricemia
Autor: | Iwao Ohno, Yoko Takeda, Yutaka Yamaguchi, Kimiyoshi Ichida, Michio Umezu, A Abe, H Hayakawa, Shohei Nakanishi, Keita Hirano, Tatsuo Hosoya, Masafumi Fukagawa |
---|---|
Rok vydání: | 2011 |
Předmět: |
Adult
Male Nephrology medicine.medical_specialty Nephrotic Syndrome Renal Tubular Transport Inborn Errors Organic Cation Transport Proteins Biopsy Urology Organic Anion Transporters Kidney urologic and male genital diseases Internal medicine medicine Humans Hypouricemia Acute tubular necrosis biology business.industry Acute kidney injury General Medicine Acute Kidney Injury Middle Aged medicine.disease Endocrinology medicine.anatomical_structure Mutation biology.protein Female Urinary Calculi SLC22A12 business Nephrotic syndrome Kidney disease |
Zdroj: | Europe PubMed Central |
ISSN: | 0301-0430 |
Popis: | Renal hypouricemia is a clinical disorder attributed to an increased renal urate excretion rate and is well known to involve a high risk of urolithiasis and exercise-induced acute kidney injury (AKI). This report concerns two interesting cases of nephrotic syndrome (NS)-induced AKI associated with renal hypouricemia. A 64-year-old female (Case 1) and a 37-year-old male (Case 2) were hospitalized because of AKI (serum creatinine: 2.07 mg/dl and 3.3 mg/dl, respectively), oliguria and NS. They were treated with prednisolone and temporary hemodialysis. Renal function improved, but hypouricemia persisted during hospitalization. Histological findings in both cases led to a diagnosis of minimal change nephrotic syndrome and identification of the diuretic phase of tubulointerstitial damage because of findings such as acute tubular necrosis. Furthermore, distal tubules of Case 2 showed an amorphous mass, possibly a uric acid crystal. Analysis of the two cases with the URAT1 gene, encoded by SLC22A12, found a homozygous mutation in exon 4 (W258stop) of each one. Our cases show that patients with renal hypouricemia may be susceptible to AKI without involvement of exercise if they possess some facilitators. Renal hypouricemic patients should therefore be carefully examined for all complications from renal hypouricemia because of high risk of AKI. |
Databáze: | OpenAIRE |
Externí odkaz: |