Literature DB >> 12677600

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

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.

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Year:  2003        PMID: 12677600     DOI: 10.1053/jpsu.2003.50151

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  1 in total

1.  [Multicystic renal tumor in a patient with WAGR syndrome].

Authors:  K-P Braun; M May; T Erler; B Hoschke
Journal:  Urologe A       Date:  2007-06       Impact factor: 0.639

  1 in total

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