Crossed renal ectopia without fusion: report of a case in a seven-month-old female infant, with review.

L. W. Falkinburg, M. N. Kay, W. Klutz
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引用次数: 4

Abstract

Crossed renal ectopia with fusion is a very rare condition, and crossed ectopia without fusion is much rarer. Review of the literature since the appearance of Wilmer's1excellent and comprehensive article in 1938 shows that this condition has been reported almost exclusively in the urologic literature, while only a very occasional report has appeared in the pediatric journals.2-4 For these reasons, and because we wish to emphasize the existence of this anomaly in differential diagnostic considerations, we feel that it is worth while to report the following case. Report of Case A 7-month-old white female infant was admitted to the Roger Williams General Hospital on Dec. 5, 1958, suffering from fever, cough, and coryza. Her family history was irrelevant. She was born eight weeks prematurely and at birth weighed 4 lb. 11 oz. She remained in the hospital for a month after birth, where her progress was satisfactory.
交叉肾异位无融合:报告1例7个月大女婴,并复习。
交叉异位合并融合是非常罕见的情况,而交叉异位不融合更为罕见。回顾自1938年Wilmer发表的一篇优秀而全面的文章以来的文献,发现这种情况几乎都是在泌尿学文献中报道的,而在儿科期刊上只有非常偶然的报道。2-4由于这些原因,也因为我们希望在鉴别诊断考虑中强调这种异常的存在,我们认为报告以下病例是值得的。一例7个月大的白人女婴于1958年12月5日因发烧、咳嗽和鼻炎入住罗杰威廉斯总医院。她的家族史与此无关。她早产了8周,出生时体重为4磅11盎司。出生后她在医院住了一个月,她的进展令人满意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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