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

Détails

Ressource 1Télécharger: BIB_8C4B96365BDF.P001.pdf (1025.14 [Ko])
Etat: Serval
Version: Final published version
ID Serval
serval:BIB_8C4B96365BDF
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Titre
Repeated surgical excision for an unusual variant of nephroblastoma: case report and review of the literature.
Périodique
Journal of pediatric surgery
Auteur(s)
Joseph J.M., Suter O.C., Nenadov-Beck M., Gudinchet F., Frey P., Meagher-Villemure K.
ISSN
1531-5037[electronic]
Statut éditorial
Publié
Date de publication
2003
Volume
38
Numéro
4
Pages
E13
Langue
anglais
Notes
Publication types: Case Reports ; Journal Article ; Review - Publication Status: ppublish
Résumé
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.
Mots-clé
Antineoplastic Combined Chemotherapy Protocols, Cell Differentiation, Combined Modality Therapy, Dactinomycin, Female, Humans, Infant, Kidney Neoplasms, Neoplasms, Multiple Primary, Nephrectomy, Remission Induction, Tomography, X-Ray Computed, Ultrasonography, Interventional, Vincristine, Wilms Tumor
Pubmed
Création de la notice
20/03/2008 10:34
Dernière modification de la notice
03/03/2018 19:13
Données d'usage