儿童孤立肾的外科治疗。

H D Jaeger, G Gutsche
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引用次数: 0

摘要

从1969年到1984年,31名儿童接受了单肾病变手术。在生命的前2年是发病率的高峰,主要是由于先天性畸形的孤立肾。相比之下,对于患病的残余肾脏,大龄儿童的手术是必要的。在一些儿童中,为了维持令人满意的器官功能,必须进行二次甚至多次手术。在1-16年的随访中,除3例尿前期患者外,其余患者肾功能均达到完全代偿。面对这些良好的手术结果,以前对孤立肾手术干预的保留意见应该被抛弃。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surgery on solitary kidneys in childhood.

From 1969 to 1984, 31 children were operated on for a diseased solitary kidney. There was a peak of incidence during the first 2 years of life, due mostly to congenitally malformed solitary kidneys. In contrast, operations in older children became necessary for diseased residual kidneys. In some children, secondary or even multiple operations had to be performed in order to maintain satisfactory organ function. Except in three preuraemic patients, renal functions were fully compensatory during a follow-up of 1-16 years. Former reservations regarding surgical intervention in solitary kidneys should be dropped in the face of these good operative results.

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