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Case Reports
. 1999 Jul;6(7):369-73.
doi: 10.1046/j.1442-2042.1999.00075.x.

Intrarenal pelvic papillary Wilms' tumor associated with aniridia: a case report

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Free article
Case Reports

Intrarenal pelvic papillary Wilms' tumor associated with aniridia: a case report

O Natsume et al. Int J Urol. 1999 Jul.
Free article

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.

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