肾内肾盂乳头状威尔姆斯瘤合并无虹膜：一例报告
Intrarenal pelvic papillary Wilms' tumor associated with aniridia: a case report.
作者信息
Natsume O, Hirao Y, Matsuda M, Okuda T
机构信息
Department of Urology, Osaka Kaisei Hospital, Japan.
出版信息
Int J Urol. 1999 Jul;6(7):369-73. doi: 10.1046/j.1442-2042.1999.00075.x.
Abstract
BACKGROUND
Intrarenal pelvic Wilms' tumor in a papillary growth is rare in children. A case of a two-year-old infant with Wilms' tumor associated with congenital aniridia is reported.
RESULTS
A chromosomal abnormality (11p13 deletion) was found in this patient. The tumor was well evaluated by ultrasonography, computed tomography and magnetic resonance imaging.
DISCUSSION
Previous case reports are briefly reviewed and the clinical characteristics disclosed.
摘要
背景
肾内肾盂乳头状生长的肾母细胞瘤在儿童中罕见。本文报告一例两岁婴儿患肾母细胞瘤并伴有先天性无虹膜。
结果
该患者发现染色体异常（11p13缺失）。通过超声、计算机断层扫描和磁共振成像对肿瘤进行了良好评估。
讨论
简要回顾了既往病例报告并揭示了临床特征。
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