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先天性巨肾盏与原发性巨输尿管并存。

The coexistence of congenital megacalyces and primary megaureter.

作者信息

Vargas B, Lebowitz R L

出版信息

AJR Am J Roentgenol. 1986 Aug;147(2):313-6. doi: 10.2214/ajr.147.2.313.

Abstract

Congenital megacalyces is a rare developmental condition of the kidney consisting of hypoplasia of the medullary pyramids and dilatation of the calyces. There is no obstruction. Primary megaureter is a form of obstructive uropathy in which there is an obstructing juxtavesical segment of ureter that is normal in caliber but that is aperistaltic. These conditions were found to occur simultaneously in the same patient six times during the past 10 years. Recognition of this rare coexistence is important so that unnecessary surgery can be avoided.

摘要

先天性巨肾盏是一种罕见的肾脏发育疾病,由髓质锥体发育不全和肾盏扩张组成。不存在梗阻。原发性巨输尿管是梗阻性尿路病的一种形式,其中输尿管膀胱壁段存在梗阻,该段输尿管管径正常但无蠕动。在过去10年中,发现这两种情况在同一患者中同时出现了6次。认识到这种罕见的共存情况很重要,这样可以避免不必要的手术。

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