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)]
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CITATION STYLE
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
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