Fused supernumerary kidney.

Fused supernumerary kidney.
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DOI:
10.2484/rcr.v6i4.552
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发表时间:
2011
影响因子:
--
通讯作者:
Dev B
Dev B
中科院分区:
其他
文献类型:
--
作者:
Suresh J;Gnanasekaran N;Dev B

文献摘要

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摘要一位35岁女性病患,经由超音波及三阶段电脑断层扫描(CT)诊断为部分融合的多余肾并双输尿管。CT还显示两条独立的肾动脉供应每个左肾和多条左肾静脉,形成一个共同的主干,流入下腔静脉。多余肾是一种罕见的先天性异常,多年来报道的病例不到100例。一个融合的多余肾更是罕见。
A partially fused supernumerary kidney with bifid ureters was diagnosed in a 35-year-old female patient using ultrasound and triple-phased computed tomography (CT). The CT also revealed two separate renal arteries supplying each of the left kidney and multiple left renal veins, forming a common trunk to drain into the inferior vena cava. Supernumerary kidney is a rare congenital anomaly; fewer than 100 cases have been reported over the years. A fused supernumerary kidney is rarer still.