Abdominal Tumors: Wilms, Neuroblastoma, Rhabdomyosarcoma, and Hepatoblastoma
- PMID: 36209742
- DOI: 10.1016/j.suc.2022.07.006
Abdominal Tumors: Wilms, Neuroblastoma, Rhabdomyosarcoma, and Hepatoblastoma
Abstract
Pediatric cancer patients have improved outcomes over the past several decades leading to a greater number of survivors living well into adulthood. Owing to their increased longevity, adult care providers are encountering childhood cancer survivors with greater frequency in their clinics and hospitals. Childhood cancer treatments are associated with varied and significant systemic complications that either persist or develop well into adulthood, including secondary malignancies, cardiomyopathies, and adhesive disease that can complicate even the simplest operation. This article reviews four of the most common solid abdominal tumors in the pediatric population and the long-term sequelae of their respective treatment regimens.
Keywords: Childhood cancer survivors; Complications; Follow-up care; Long-term sequelae; Pediatric solid tumors.
Copyright © 2022 Elsevier Inc. All rights reserved.
Conflict of interest statement
Disclosure J.T. Castle is funded by the NIH Training Grant T32CA160003.
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