Open Access
RESIDENT’S CORNER
A rare case of adult Wilms’ tumor
Tin C. Ngo1, Curtis J. Clark1, Gary Zhao2, Jeffrey H. Reese3
1
Department of Urology, Stanford University School of Medicine, Stanford, California, USA
2
Division of Oncology, Santa Clara Valley Medical Center, San Jose, California, USA
3
Division of Urology, Santa Clara Valley Medical Center, San Jose, California, USA
Address correspondence to Dr. Tin C. Ngo, Department of
Urology, Stanford University School of Medicine, 300 Pasteur
Drive, S-287, Stanford, CA 94305 USA
Canadian Journal of Urology 2011, 18(1), 5568-5569.
Abstract
Although Wilms’ tumor is the most common primary
renal malignancy in children, it is exceedingly rare in
adults and has an estimated incidence of less than 0.2
cases per million. Little is known about the biology of
this tumor in adults and clinicians have had to rely on
pediatric treatment protocols. Overall, prognosis is worse
in adults, though like in children, unfavorable histology
and higher stage at presentation confer a worse prognosis.
Keywords
Wilms’ tumor, nephroblastoma, adult
Cite This Article
APA Style
Ngo, T.C., Clark, C.J., Zhao, G., Reese, J.H. (2011). A rare case of adult Wilms’ tumor. Canadian Journal of Urology, 18(1), 5568–5569.
Vancouver Style
Ngo TC, Clark CJ, Zhao G, Reese JH. A rare case of adult Wilms’ tumor. Can J Urology. 2011;18(1):5568–5569.
IEEE Style
T.C. Ngo, C.J. Clark, G. Zhao, and J.H. Reese, “A rare case of adult Wilms’ tumor,” Can. J. Urology, vol. 18, no. 1, pp. 5568–5569, 2011.
Copyright © 2011 The Canadian Journal of Urology.