| Literature DB >> 12677600 |
J M Joseph1, O C Suter, M Nenadov-Beck, F Gudinchet, P Frey, K Meagher-Villemure.
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. Copyright 2003, Elsevier Science (USA). All rights reserved.Entities:
Mesh:
Substances:
Year: 2003 PMID: 12677600 DOI: 10.1053/jpsu.2003.50151
Source DB: PubMed Journal: J Pediatr Surg ISSN: 0022-3468 Impact factor: 2.545