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Case Study

机译:案例分析

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摘要

An 8-year-old white girl is referred for evaluation of hematuria, proteinuria, and hypertension. She has had recurrent episodes of gross hematuria. The first was at 3 years of age and was attributed to a urinary tract infection, but a urine culture was negative. She was treated with 10 days of antibiotics, and the symptoms resolved. The second episode, at age 5 years, was attributed to acute poststreptococcal glomerulonephritis, although an antistreptolysin O (ASO) titer was normal, and complement studies were not ordered. Blood pressure at that time was 120/80 mm Hg (normal for age and height is 94/54 mm Hg). The girl was lost to follow-up and presents 3 years later with blood pressure at the 95th percentile, gross hematuria, and generalized edema. Urinalysis of tea-colored urine shows too-numerous-to-count dysmor-phic red blood cells (RBCs), white blood cells, proteinuria, and RBC casts. The differential diagnosis includes immunoglobulin A nephropathy, membranoproliferative glomerulonephritis, and hereditary nephritis, although the latter condition is unusual in a female. She is admitted for additional evaluation.
机译:一名8岁的白人女孩因血尿,蛋白尿和高血压而被评估。她反复发作肉眼血尿。第一次是在3岁时,归因于尿路感染,但尿培养阴性。她接受了10天的抗生素治疗,症状得以缓解。尽管抗链球菌溶血素O(ASO)滴度正常,并且没有进行补充研究,但5岁时的第二次发作归因于急性链球菌性肾小球肾炎。当时的血压为120/80毫米汞柱(年龄和身高正常为94/54毫米汞柱)。该女孩失访,并于3年后出现95%的血压,严重血尿和全身性水肿。茶色尿液的尿液分析显示,数量过多的营养不良性红细胞(RBC),白细胞,蛋白尿和RBC铸型。鉴别诊断包括免疫球蛋白A肾病,膜增生性肾小球肾炎和遗传性肾炎,尽管后者在女性中不常见。她被接受进一步评估。

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