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Red urine, updated for the nephrologist: a case report
Alexandre Le Joncour1,2, Laurent Mesnard3, Alexandre Hertig3
1Department of Nephrology and Renal Transplantation, Hôpital universitaire Tenon, AP-HP, Université Pierre et Marie Curie, Paris, France. lejoncour.alexandre@gmail.com.
Background:
Sickle cell trait is not completely benign, and some renal complications can occur. The baseline rate of admission for gross hematuria in normal males carrying the sickle cell trait is 2%.
Case Presentation:
A 35-year-old non-smoking African man experienced a 2-week history of painless, profuse and persistent gross hematuria. Laboratory tests showed normal renal function, hematuria and mild proteinuria. Abdominal ultrasonography and computed tomography angiography revealed no renal abnormalities; the bladder appeared pristine under cystoscopy. The diagnosis of sickle cell trait associated with gross hematuria was made using hemoglobin electrophoresis; renal biopsy and its complications were avoided. Urine was clear after 2 weeks of oral hydration and gamma epsilon-aminocaproic acid.
Conclusion:
Hemoglobin electrophoresis should be performed in cases of gross hematuria. Coupled with other non-invasive evaluation, this could avoid renal biopsy and its associated complications.
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