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首页> 外文期刊>Journal of Korean medical science. >Unilateral Autosomal Dominant Polycystic Kidney Disease with Contralateral Renal Agenesis: A Case Report
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Unilateral Autosomal Dominant Polycystic Kidney Disease with Contralateral Renal Agenesis: A Case Report

机译:单侧常染色体显性多囊肾合并对侧肾发育不全的病例报告

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Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease. There are some reports in the literature concerning unilateral ADPKD. However, in adults, only a few cases of unilateral ADPKD with agenesis of contralateral kidney have been reported. We present a case of unilateral ADPKD with agenesis of contralateral kidney in a 66-yr-old man. Radiographic images showed the enlarged right kidney with multiple variable-sized cysts and the absence of the left kidney. The diagnosis of ADPKD was confirmed by the family screening. The patient received maintenance hemodialysis for endstage renal disease. We report a case of unilateral ADPKD associated with contralateral renal agenesis in a 66-yr-old male patient with a literature review.
机译:常染色体显性遗传性多囊肾病(ADPKD)是最常见的遗传性肾病。文献中有一些有关单方面ADPKD的报道。然而,在成年人中,仅报道了少数伴有对侧肾脏发育不全的单侧ADPKD病例。我们提出了一个66岁男性单侧ADPKD与对侧肾脏发育不全的病例。影像学检查显示右肾肿大,囊肿多发,左肾不存在。通过家族筛查证实了ADPKD的诊断。该患者因终末期肾脏疾病接受了维持性血液透析。我们报道了66例男性患者单侧ADPKD与对侧肾不发育相关的病例,并进行了文献复习。

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