尿素使一名患有血红蛋白C性状的15岁青少年的肉眼血尿消退。

Urea resolves gross hematuria in a 15 year old with hemoglobin C trait.

作者信息

Sakarcan A, Stallworth J

机构信息

Department of Pediatrics, University of South Carolina School of Medicine, Columbia, USA.

出版信息

Pediatr Nephrol. 2001 Feb;16(2):145-7. doi: 10.1007/s004670000532.

DOI:10.1007/s004670000532

PMID:11261682

Abstract

Hematuria is a rare complication seen in patients with hemoglobin C trait. We report a 15-year-old African-American female with hemoglobin C trait, who presented with persistent hematuria. None of the urological, serological or histological workups revealed any other pathology. Hematuria failed to respond to all conventional modalities used in the treatment of the same condition seen in sickling hemoglobinopathies. This case is the first known case of persistent hematuria in a pediatric patient with hemoglobin C trait, which resolved with intravenous urea administration.

摘要

血尿是血红蛋白C性状患者中罕见的并发症。我们报告一名患有血红蛋白C性状的15岁非裔美国女性，她出现持续性血尿。泌尿外科、血清学或组织学检查均未发现任何其他病理情况。对于镰状血红蛋白病中出现的相同病症，血尿对所有常规治疗方式均无反应。该病例是已知首例患有血红蛋白C性状的儿科患者出现持续性血尿，经静脉注射尿素后血尿得以缓解。