Wilms Tumor (Nephroblastoma), Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.

  title={Wilms Tumor (Nephroblastoma), Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.},
  author={Frank M. Balis and Daniel M. Green and Clarke P. Anderson and Shelly Cook and Jasreman Dhillon and Kenneth William Gow and Susan M. Hiniker and Rama Jasty-Rao and Chi Lin and H. Lovvorn and Iain J MacEwan and Julian A. Martinez-Agosto and Elizabeth Mullen and Erin S. Murphy and Mark A. Ranalli and Daniel S. Rhee and Denise A. Rokitka and Elizabeth Tracy and Tamara Z. Vern-Gross and Michael F. Walsh and Amy L. Walz and Jonathan E. Wickiser and Matthew A. Zapala and Ryan A Berardi and Miranda J. Hughes},
  journal={Journal of the National Comprehensive Cancer Network : JNCCN},
  volume={19 8},
  • F. Balis, D. Green, M. Hughes
  • Published 1 August 2021
  • Medicine
  • Journal of the National Comprehensive Cancer Network : JNCCN
The NCCN Guidelines for Wilms Tumor focus on the screening, diagnosis, staging, treatment, and management of Wilms tumor (WT, also known as nephroblastoma). WT is the most common primary renal tumor in children. Five-year survival is more than 90% for children with all stages of favorable histology WT who receive appropriate treatment. All patients with WT should be managed by a multidisciplinary team with experience in managing renal tumors; consulting a pediatric oncologist is strongly… 
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