Kidney Preservation and Wilms Tumor Development in Children with Diffuse Hyperplastic Perilobar Nephroblastomatosis: A Report from the Children’s Oncology Group Study AREN0534

Author:

Ehrlich Peter F.,Tornwall Brett,Chintagumpala Murali M.,Chi Yueh-Yun,Hoffer Fredric A.,Perlman Elizabeth J.,Kalapurakal John A.,Warwick Anne,Shamberger Robert C.,Khanna Geetika,Hamilton Thomas E.,Gow Kenneth W.,Paulino Arnold C.,Gratias Eric J.,Mullen Elizabeth A.,Geller James I.,Fernandez Conrad V.,Dome Jeffrey S.

Funder

Statistics & Data Center Grant

Human Specimen Banking in NCI-Sponsored Clinical Trials

NCTN Statistics & Data Center

Chair's Grant

NCTN Network Group Operations Center Grant

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Surgery

Reference23 articles.

1. Cancer Statistics. 2019 [cited September 27 2019]. https://seer.cancer.gov/.

2. Dome JS, Perlman EJ, Ritchey ML, et al. Renal Tumors. In: PA Pizzo, DG Poplack, editors., et al., Principles and practice of pediatric oncology, vol 7, Philadelphia, PA: Lippincott Williams and Wilkins; 2015. p. 753–72.

3. Beckwith JB, Kiviai NB, Bonadio JF. Nephrogenic rests, nephroblastomatosis and the pathogenesis of Wilms tumor. Pediatric Pathology. 1990;10:1–36.

4. Beckwith JB. National Wilms Tumor study: an update for pathologists. Pediatr Dev Path. 1998;1:79–84.

5. Perlman E, Faria P, Soares A, Offer FA. Hyperplastic perilobar nephroblastomatosis: long-term survival in 52 patients. Pediatr Blood Cancer. 2006;46:203–21.

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