Literature DB >> 10445307

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

O Natsume1, Y Hirao, M Matsuda, T Okuda.   

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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Year:  1999        PMID: 10445307     DOI: 10.1046/j.1442-2042.1999.00075.x

Source DB:  PubMed          Journal:  Int J Urol        ISSN: 0919-8172            Impact factor:   3.369


  1 in total

1.  Botryoid Wilms tumor: a non-existent "entity" causing diagnostic and staging difficulties.

Authors:  Gordan M Vujanić; Marco Schiavo Lena; Neil J Sebire
Journal:  Virchows Arch       Date:  2018-12-04       Impact factor: 4.064

  1 in total

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