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两例血红蛋白 C 特征血尿病例。

Two cases of hematuria with hemoglobin C trait.

机构信息

Department of Pediatrics, University of Tennessee Health Science Center, Memphis, TN, USA.

出版信息

Pediatr Nephrol. 2009 Dec;24(12):2455-7. doi: 10.1007/s00467-009-1263-1. Epub 2009 Aug 11.

Abstract

Patients with sickle cell disease commonly experience painless hematuria. Hematuria may be found in patients with sickle cell trait, sickle cell anemia, and sickle cell hemoglobin C disease, but it is believed to be uncommon in patients with other hemoglobinopathies, such as hemoglobin C disease and hemoglobin C trait. We report two cases of children with hemoglobin C trait who presented with persistent painless hematuria. Because it is possible that hematuria in a patient with hemoglobin C trait is purely coincidental, all patients with a hemoglobinopathy and hematuria should undergo a complete evaluation so as not to overlook other causes of hematuria.

摘要

镰状细胞病患者常出现无痛性血尿。镰状细胞特征、镰状细胞贫血和镰状细胞血红蛋白 C 病患者可出现血尿,但据信其他血红蛋白病(如血红蛋白 C 病和血红蛋白 C 特征)患者血尿不常见。我们报告了两例血红蛋白 C 特征的儿童持续性无痛性血尿。因为血红蛋白 C 特征患者的血尿可能纯属巧合,所以所有血红蛋白病和血尿患者均应进行全面评估,以免漏诊其他血尿原因。

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