Next Article in Journal
Ferroptosis Induction and YAP Inhibition as New Therapeutic Targets in Gastrointestinal Stromal Tumors (GISTs)
Next Article in Special Issue
Young-Onset Cancers—Early Steps in the Right Direction
Previous Article in Journal
Quantum Dot-Based Screening Identifies F3 Peptide and Reveals Cell Surface Nucleolin as a Therapeutic Target for Rhabdomyosarcoma
Previous Article in Special Issue
Variation in Treatment Patterns of Patients with Early-Onset Gastric Cancer
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Pediatric Neuroendocrine Neoplasms: Rare Malignancies with Incredible Variability

1
Department of Surgery, Markey Cancer Center, University of Kentucky, 800 Rose Street, Lexington, KY 40536, USA
2
Department of Surgery, University of Kentucky, 800 Rose Street, Lexington, KY 40536, USA
3
Department of Internal Medicine-Medical Oncology, Markey Cancer Center, University of Kentucky, 800 Rose Street, Lexington, KY 40536, USA
*
Author to whom correspondence should be addressed.
Cancers 2022, 14(20), 5049; https://doi.org/10.3390/cancers14205049
Submission received: 21 September 2022 / Revised: 7 October 2022 / Accepted: 13 October 2022 / Published: 15 October 2022
(This article belongs to the Special Issue Young-Onset GI Cancer)

Simple Summary

Neuroendocrine neoplasms are increasing in incidence at a remarkable rate meaning more providers are encountering them in both adult and pediatric patients. This classification of neoplasm encompasses a wide range of different malignancies with a variety of symptoms at presentation and each treated differently. Additionally, over the past few years there has been a change in classification of these neoplasms and a variety of changes and advances in how they are treated. Given this and their rarity in pediatric patients, healthcare providers may not be familiar with these changes. Our goal with this review was to provide an overview of all the most commonly encountered forms of neuroendocrine neoplasms in pediatric patients with up to date recommendations so any healthcare provider can quickly and accurately acclimate themselves.

Abstract

Neuroendocrine neoplasms (NENs) encompass a variety of neuroendocrine tumors (NETs) and neuroendocrine carcinomas (NECs) which can arise anywhere in the body. While relatively rare in the pediatric population, the incidence of NENs has increased in the past few decades. These neoplasms can be devastating if not diagnosed and treated early, however, symptoms are variable and can be indolent for many years. There is a reported median of 10 years from the appearance of the first symptoms to time of diagnosis. Considering some of these neoplasms have a mortality rate as high as 90%, it is crucial healthcare providers are aware of NENs and remain vigilant. With better provider education and easily accessible resources for information about these neoplasms, awareness can be improved leading to earlier disease recognition and diagnosis. This manuscript aims to provide an overview of both the most common NENs as well as the rarer NENs with high lethality in the pediatric population. This review provides up to date evidence and recommendations, encompassing recent changes in classification and advances in treatment modalities, including recently completed and ongoing clinical trials.
Keywords: pediatric; neuroendocrine neoplasms; neuroendocrine tumors; neuroendocrine carcinomas pediatric; neuroendocrine neoplasms; neuroendocrine tumors; neuroendocrine carcinomas

Share and Cite

MDPI and ACS Style

Castle, J.T.; Levy, B.E.; Chauhan, A. Pediatric Neuroendocrine Neoplasms: Rare Malignancies with Incredible Variability. Cancers 2022, 14, 5049. https://doi.org/10.3390/cancers14205049

AMA Style

Castle JT, Levy BE, Chauhan A. Pediatric Neuroendocrine Neoplasms: Rare Malignancies with Incredible Variability. Cancers. 2022; 14(20):5049. https://doi.org/10.3390/cancers14205049

Chicago/Turabian Style

Castle, Jennifer T., Brittany E. Levy, and Aman Chauhan. 2022. "Pediatric Neuroendocrine Neoplasms: Rare Malignancies with Incredible Variability" Cancers 14, no. 20: 5049. https://doi.org/10.3390/cancers14205049

APA Style

Castle, J. T., Levy, B. E., & Chauhan, A. (2022). Pediatric Neuroendocrine Neoplasms: Rare Malignancies with Incredible Variability. Cancers, 14(20), 5049. https://doi.org/10.3390/cancers14205049

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop