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儿童特发性高钙尿症与无症状肉眼血尿的关联。

The association of idiopathic hypercalciuria and asymptomatic gross hematuria in children.

作者信息

Kalia A, Travis L B, Brouhard B H

出版信息

J Pediatr. 1981 Nov;99(5):716-9. doi: 10.1016/s0022-3476(81)80390-3.

Abstract

Seven children with asymptomatic gross hematuria are described. Six had recurrent hematuria; one had a single episode. Occasional global glomerulosclerosis and/or mesangial electron dense deposits were present in the three patients in whom renal biopsy was performed; the changes were felt to be insufficient to account for the hematuria. None of the patients had urolithiasis or any significant urinary tract abnormality. One was an adopted child; a family history of urolithiasis was obtained in the other six. Idiopathic hypercalciuria was documented in six patients; the seventh subsequently passed a calcium oxalate calculus. One patient is 10 weeks of age at the time of this submission. Of the remainder, three patients received no specific therapy; renal calculi developed six months, six years, and eight years later. Three patients were treated with a thiazide diuretic soon after onset of hematuria and confirmation of idiopathic hypercalciuria; there was complete cessation of hematuria within five days with no recurrence as long as therapy was continued. We suggested that measurement of urinary calcium excretion as part of the initial evaluation of a child with gross hematuria may, in some cases, obviate invasive investigations and allow for effective therapy.

摘要

本文描述了7例无症状肉眼血尿患儿。其中6例有复发性血尿,1例为单次发作。在接受肾活检的3例患者中,偶尔可见全球性肾小球硬化和/或系膜电子致密沉积物;这些改变被认为不足以解释血尿的原因。所有患者均无尿路结石或任何明显的尿路异常。1例为领养儿童,其他6例有尿路结石家族史。6例患者被证实患有特发性高钙尿症;第7例随后排出了草酸钙结石。在提交本文时,1例患者为10周龄。其余患者中,3例未接受特殊治疗;分别在6个月、6年和8年后出现肾结石。3例患者在血尿发作并确诊为特发性高钙尿症后不久接受了噻嗪类利尿剂治疗;血尿在5天内完全停止,只要继续治疗就不会复发。我们建议,在对肉眼血尿患儿进行初步评估时,测定尿钙排泄量在某些情况下可能避免进行侵入性检查,并能实现有效治疗。

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