Wilms Tumor Ppt New -

References (select textbooks/guidelines): current pediatric oncology protocols (COG, SIOP), major pediatric oncology textbooks, and peer-reviewed reviews.

This article provides a structured, evidence-based outline for a state-of-the-art presentation. wilms tumor ppt new

The exact cause of Wilms tumor is not known, but several risk factors have been identified. These include: These include: | Feature | Wilms Tumor |

| Feature | Wilms Tumor | Mesoblastic Nephroma | Rhabdoid Tumor | Clear Cell Sarcoma | |---------|-------------|----------------------|----------------|--------------------| | Age | 1–5 yrs | <3 months | <2 yrs | 1–4 yrs | | Prognosis | Excellent | Excellent | Poor (brain mets) | Intermediate | | Histology | Triphasic | Spindle cells | Eosinophilic inclusions | Clear cells | | Association | WT1, Beckwith-Wiedemann | None | INI1 mutation | YWHAE fusion | 3 months | &lt

The cure rate is excellent, but survivors require lifelong monitoring for: Monitoring for chronic kidney disease. Cardiotoxicity: If Doxorubicin or chest radiation was used.