Abstract
Nephron-sparing surgery (NSS) is the treatment of choice for children with bilateral Wilms' tumor (WT), or with WT on a single kidney, or with WT and a disease of the contralateral kidney, or with benign kidney tumor. NSS is a reasonable alternative to nephrectomy in children at risk of metachronous WT, including children with genetic syndromes, children younger than 1 year of age, and children with hyperplastic nephroblastomatosis. The use of NSS in selected children with "low-risk" or stage I "intermediate-risk" WT and a normal contralateral kidney is still controversial. Available data suggest that, in children with WT, NSS does not impair the outcome and has a renal function advantage over nephrectomy.
| Original language | English |
|---|---|
| Pages (from-to) | 3-9 |
| Number of pages | 7 |
| Journal | Seminars in pediatric surgery |
| Volume | 15 |
| Issue number | 1 |
| DOIs | |
| State | Published - Feb 2006 |
Keywords
- Congenital mesoblastic nephroma
- Cystic nephroma
- Cystic partially differentiated nephroblastoma
- Enucleation
- Nephroblastoma
- Nephroblastomatosis
- Oncocitoma
- Partial nephrectomy
- Wilms' tumor