Pediatric papillary thyroid cancer: Current management challenges

Publication date

2017

Authors

Verburg, Frederik A.
Van Santen, Hanneke M.ORCID 0000-0002-6773-6931ISNI 0000000387710357
Luster, Markus

Editors

Advisors

Supervisors

Document Type

Article

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Abstract

Although with a standardized incidence of 0.54 cases per 100,000 persons, differentiated thyroid cancer (DTC) is a rare disease in children and adolescents, it nonetheless concerns ~1.4% of all pediatric malignancies. Furthermore, its incidence is rising. Due to the rarity and long survival of pediatric DTC patients, in most areas of treatment little evidence exists. Treatment of pediatric DTC is therefore littered with controversies, many questions therefore remain open regarding the optimal management of pediatric papillary thyroid cancer (PTC), and many challenges remain unsolved. In the present review, we aim to provide an overview of these challenging areas of patient and disease management in pediatric PTC patients. Data on diagnosis, surgery, radionuclide, and endocrine therapy are discussed, and the controversies therein are highlighted.

Keywords

Follow-up, I-131 therapy, Papillary thyroid cancer, Pediatric cancer, Survival, Treatment, Oncology, Pharmacology (medical), Review, Journal Article

Citation

Verburg, F A, Van Santen, H M & Luster, M 2017, 'Pediatric papillary thyroid cancer : Current management challenges', OncoTargets and Therapy, vol. 10, pp. 165-175. https://doi.org/10.2147/OTT.S100512