Repeated surgical excision for an unusual variant of nephroblastoma: Case report and review of the literature

  • Joseph J
  • Suter O
  • Nenadov-Beck M
  • et al.
N/ACitations
Citations of this article
9Readers
Mendeley users who have this article in their library.

Abstract

Bilateral fetal rhabdomyomatous nephroblastoma is a rare variant of Wilms' Tumor. The authors report the evolution over 48 months of a 10-month-old baby with bilateral nephroblastoma for which a left nephrectomy was initially performed. A right kidney tumor was enucleated preserving the kidney. The transformation of the primary tumor into a completely differentiated cystic nephroblastoma or nephromalike tumor and the appearance of a metachronous lesion was seen. This report emphasizes the role of nephron-sparing surgery in bilateral Wilms' Tumor when a benign transformation occurs under chemotherapy.[on SciFinder (R)]

Cite

CITATION STYLE

APA

Joseph, J. M., Suter, O. C., Nenadov-Beck, M., Gudinchet, F., Frey, P., & Meagher-Villemure, K. (2003). Repeated surgical excision for an unusual variant of nephroblastoma: Case report and review of the literature. Journal of Pediatric Surgery, 38(4), 13–16. https://doi.org/10.1053/jpsu.2003.50151

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free