Intrarenal pelvic papillary Wilms' tumor associated with aniridia: a case report
- PMID: 10445307
- DOI: 10.1046/j.1442-2042.1999.00075.x
Intrarenal pelvic papillary Wilms' tumor associated with aniridia: a case report
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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