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Review Case Reports
Repeated surgical excision for an unusual variant of nephroblastoma: case report and review of the literature.
- J M Joseph, O C Suter, M Nenadov-Beck, F Gudinchet, P Frey, and K Meagher-Villemure.
- Department of Pediatric Surgery, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
- J. Pediatr. Surg. 2003 Apr 1; 38 (4): E13.
AbstractBilateral 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.
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