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Repeated surgical excision for an unusual variant of nephroblastoma: case report and review of the literature
Authors:Joseph J M  Suter O C  Nenadov-Beck M  Gudinchet F  Frey P  Meagher-Villemure K
Affiliation:Departments of Pediatric Surgery, Pathology, Pediatric Oncology, and Radiology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland
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.
Keywords:Nephron-sparing surgery   fetal rhabdomyomatous nephroblastoma   Wilms' tumor   cystic partially differentiated nephroblastoma   multicystic nephromalike tumor
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