首页> 外文期刊>The Journal of Urology >Supranormal renographic differential renal function in congenital hydronephrosis: fact, not artifact.
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Supranormal renographic differential renal function in congenital hydronephrosis: fact, not artifact.

机译:先天性肾积水肾功能异常肾功能异常:事实,不是伪影。

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PURPOSE: Children with unilateral hydronephrosis, who had been prospectively examined with diethylenetriaminepentaacetic acid (DTPA) and dimercapto-succinic acid (DMSA) renography, were evaluated to determine whether supranormal renographic differential renal function exists. MATERIALS AND METHODS: A total of 54 children with congenital single system hydronephrosis underwent abdominal ultrasound, voiding cystourethrogram, and DTPA and DMSA renal scans. None had abnormalities of the bladder or contralateral kidney. Differential renal function greater than 55% was defined as supranormal. RESULTS: Of the 54 patients 15 (28%) with a median age of 4 months (range 0.5 to 66) were identified with supranormal renographic renal function on either DTPA or DMSA. Supranormal renographic renal function was detected by DMSA in 9 cases (mean 57+/-2%), DTPA in 8 (mean 58+/-2%) and both in 2 (mean 57+/-2%). Average function demonstrated in the 15 patients was 55+/-3% (range 51 to 62) with DMSA which was not different from that found with DTPA (mean 55+/-4%, range 46 to 61%). The kidneys with supranormal renographic renal function were significantly larger than hydronephrotic controls according to longitudinal parenchymal area on DMSA. Mean followup was 20 months for 13 patients, with 8 of 13 (62%) undergoing pyeloplasty. Followup DTPA renal scans available in 9 children revealed persistent supranormal function in 6, despite pyeloplasty in 3. CONCLUSIONS: Supranormal renographic differential renal function does exist in congenital hydronephrosis and when found the kidneys are consistently enlarged. The position of supranormal renographic renal function in the management algorithm of hydronephrosis remains to be elucidated as it does not appear to be a benign prognostic factor.
机译:目的:对单侧肾积水的儿童进行了前瞻性的二亚乙基三胺五乙酸(DTPA)和二巯基琥珀酸(DMSA)肾造影检查,以评估是否存在肾功能异常肾功能异常。材料与方法:共有54例先天性单系统肾积水患儿接受了腹部超声检查,排尿膀胱造影,以及DTPA和DMSA肾脏扫描。没有人有膀胱或对侧肾脏异常。肾功能差异大于55%被定义为超正常。结果:54例患者中有15例(28%)的中位年龄为4个月(0.5到66岁),其DTPA或DMSA肾功能肾功能超常。 DMSA检出肾功能异常正常者9例(平均57 +/- 2%),DTPA检出8例(平均58 +/- 2%),两者均检出2例(平均57 +/- 2%)。在15名患者中,DMSA的平均功能为55 +/- 3%(范围为51至62),与DTPA的平均功能相同(平均值为55 +/- 4%,范围为46至61%)。根据DMSA上的纵向实质区域,肾肾功能超正常的肾脏明显大于肾积水对照。 13例患者平均随访20个月,其中13例中有8例(62%)接受了肾盂成形术。 9例儿童的DTPA肾脏扫描结果显示,尽管有3例行肾盂成形术,但仍有6例持续超正常功能。结论:先天性肾积水确实存在肾功能异常肾功能异常,发现肾脏持续增大。超肾功能肾功能在肾积水的治疗方法中的位置尚待阐明,因为它似乎不是良性的预后因素。

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