双侧肾盂切开术治疗双侧D-J支架周围胱氨酸结石一例无尿婴儿

E. S. Pelit, A. Yıldırım, G. Atis, C. Çanakcı, E. Başok, T. Çaşkurlu
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引用次数: 0

摘要

胱氨酸尿症是一种遗传性疾病,胱氨酸和二碱性氨基酸(赖氨酸、精氨酸、鸟氨酸)通过肾小管和肠道的管腔膜运输,导致复发性肾结石。本病的主要临床表现是反复出现胱氨酸结石。胱氨酸结石通常发生在生命的第二或第三个十年,偶尔发生在婴儿期。肾结石的非典型症状如无尿症可在婴儿期变得明显。双侧胱氨酸结石引起婴幼儿急性无尿极为罕见。我们报告了第一例双侧肾盂切开术治疗胱氨酸结石和影响双侧双j (DJ)支架的婴儿无尿症。在我们的患者中,DJ支架被移除,并成功实现无结石状态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bilateral pyelolitotomy for cystine stones encircling the bilateral D-J stents in an infant presenting with anuria
SUMMARY Cystinuria is a hereditary disorder of cystine and dibasic amino acids (lysine, arginine, ornithine) transport across the luminal membrane of renal tubules and intestine, resulting in recurrent nephrolithiasis. Predominant clinical finding of this disease is the occurrence of recurrent cystine stones. Cystine stones frequently occur in the second or third decade of life with an occasional occurrence in infancy. Atypical symptoms of renal stones as anuria can become apparent in infancy. Bilateral cystine stones causing acute anuria in infants are extremely rare. We report the first case of bilateral pyelolitotomy performed for cystine stone and impacted bilateral double-J (DJ) stents in an infant presenting with anuria. In our patients DJ stents were removed, and a stone-free state was successfully achieved.
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