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Thyroid Cancer in Children and Adolescents

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Pediatric Endocrinology

Part of the book series: Contemporary Endocrinology ((COE))

Abstract

Thyroid cancer is rare in childhood and adolescence and consists of several histopathologic groups that differ considerably in their clinical behavior. Major pathologic categories include differentiated, medullary, and poorly differentiated thyroid carcinomas. Medullary carcinoma accounts for a small percentage of pediatric thyroid cancers. It is most often diagnosed in children and adolescents affected by MEN IIa, MEN IIb, or Familial Medullary Carcinoma syndromes. These autosomal dominant disorders are known to be caused by mutations in the RET proto-oncogene; molecular screening is now available for individuals who, based on family history, are felt to be at risk (1). Poorly differentiated thyroid cancers, including anaplastic and insular carcinomas, are fortunately exceedingly uncommon in the pediatric age group but carry a very poor prognosis (2). Differentiated thyroid cancers account for the vast majority of thyroid cancers of youth and will be the focus of this review.

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Sklar, C.A., La Quaglia, M.P. (2003). Thyroid Cancer in Children and Adolescents. In: Radovick, S., MacGillivray, M.H. (eds) Pediatric Endocrinology. Contemporary Endocrinology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-336-1_19

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  • DOI: https://doi.org/10.1007/978-1-59259-336-1_19

  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-1-61737-268-1

  • Online ISBN: 978-1-59259-336-1

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