Literature DB >> 6502822

Recurrent hematuria in 4 white patients with sickle cell trait.

E Oksenhendler, B Bourbigot, F Desbazeille, D Droz, C Choquenet, R Girot, P Jungers.   

Abstract

Extensive investigations failed to disclose the etiology of recurrent gross hematuria in 4 white patients of Algerian descent. Hemoglobin electrophoresis revealed sickle cell trait in all cases. The hematuria ceased after bed rest and hydration in 3 patients, and following partial nephrectomy after visualization of the bleeding site at operative nephroscopy in 1. We recommend that hemoglobin electrophoresis be considered when evaluating every patient, black or white, presenting with unexplained hematuria.

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Year:  1984        PMID: 6502822     DOI: 10.1016/s0022-5347(17)50097-x

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  3 in total

1.  Sickle cell trait, hemoglobin C trait, and invasive pneumococcal disease.

Authors:  Katherine A Poehling; Laney S Light; Melissa Rhodes; Beverly M Snively; Natasha B Halasa; Ed Mitchel; William Schaffner; Allen S Craig; Marie R Griffin
Journal:  Epidemiology       Date:  2010-05       Impact factor: 4.822

Review 2.  The nephropathy of sickle cell trait and sickle cell disease.

Authors:  Kenneth I Ataga; Santosh L Saraf; Vimal K Derebail
Journal:  Nat Rev Nephrol       Date:  2022-02-21       Impact factor: 42.439

Review 3.  Sickle cell disease and the kidney.

Authors:  Jon I Scheinman
Journal:  Nat Clin Pract Nephrol       Date:  2008-12-02
  3 in total

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