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一名具有镰状细胞性状的青少年患肾髓质癌。

Renal medullary carcinoma in an adolescent with sickle cell trait.

作者信息

Warren K E, Gidvani-Diaz V, Duval-Arnould B

机构信息

National Cancer Institute, and National Naval Medical Center, Department of Pediatrics, Bethesda, Maryland, USA.

出版信息

Pediatrics. 1999 Feb;103(2):E22. doi: 10.1542/peds.103.2.e22.

Abstract

We describe the complex presentation of a patient with renal medullary carcinoma, a newly described entity primarily affecting young patients with sickle cell trait. Renal medullary carcinoma is an aggressive, rapidly destructive tumor associated with a delayed diagnosis and a poor outcome. The most common presenting signs and symptoms include hematuria, abdominal or flank pain, and weight loss. Sickle cell trait as the sole cause of hematuria in young black patients is a diagnosis of exclusion. Hemoglobin electrophoresis, intravenous pyelography, and computed tomography scans should be the minimal studies performed in young black patients with hematuria.

摘要

我们描述了一名患有肾髓质癌患者的复杂临床表现,肾髓质癌是一种新发现的主要影响具有镰状细胞特征的年轻患者的疾病。肾髓质癌是一种侵袭性、快速破坏性肿瘤,诊断往往延迟且预后较差。最常见的症状和体征包括血尿、腹部或侧腹痛以及体重减轻。镰状细胞特征作为年轻黑人患者血尿的唯一原因是一种排除性诊断。血红蛋白电泳、静脉肾盂造影和计算机断层扫描应是对年轻血尿黑人患者进行的最少检查项目。

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