A novel Wilms’ tumor
✍ Scribed by Nicole Wagner; Kay-Dietrich Wagner; Mickael Afanetti; Fabien Nevo; Corinne Antignac; Jean-Francois Michiels; Andreas Schedl; Etienne Berard
- Publisher
- Springer
- Year
- 2008
- Tongue
- English
- Weight
- 990 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0931-041X
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📜 SIMILAR VOLUMES
Wilms tumor (WT), a sporadic and familial childhood kidney tumor, is genetically heterogeneous. One WT gene, WT1 at 11p13, has been cloned, but only a minority of WTs carry detectable mutations at that locus. WT1 can also be excluded as the predisposition gene in most WT families, implying the exist
## Abstract Wilms tumor (WT), an embryonic tumor arising from undifferentiated renal mesenchyme, has been a productive model for understanding the role of genes in both tumorigenesis and normal organogenesis. Approximately 2% of WT patients have a family history of WT, and even sporadic WT is thoug
A 17-month-old black male, who had bilateral Wilms tumor diagnosed nine months earlier, was presented for consideration of further therapy. He was first seen when eight months of age because of a right-sided abdominal mass. There was no hematuria and his blood pressure was normal at that time. The
Two well-documented cases of Wilms' tumor in adult patients are reported. Surgery remains the treatment of choice in stage I cases with favorable cell differentiation. Adjuvant therapy with chemotherapy or radiation may be necessary in patients beyond stage I or when the cell differentiation is more
A retroperitoneal extrarenal Wilms tumor arising from an embryonic crest of renal tissue on a 10-year-old boy is reported. The histogenesis of such tumor is discussed.