Surgery for medullary thyroid cancer

Kathryn J. Rowland, Jeffrey F. Moley

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

Abstract

Medullary thyroid cancer (MTC) is a neuroendocrine malignancy of the calcitonin producing thyroid C cells, accounting for 5-10% of all thyroid cancers. While the majority of cases are sporadic (75%), hereditary syndromes account for 25% of all cases and should be considered whenever evaluating a patient. Compared to differentiated thyroid cancer, MTC is more aggressive yet remains a relatively indolent malignancy, with 10-year survival rates reported from 69% to 89%. Sporadic cases usually present with a palpable thyroid mass. Hereditary cases may be detected and treated on the basis of a genomic diagnosis once the syndrome is diagnosed in a family. Unlike differentiated thyroid cancer, there is no known effective systemic therapy for medullary thyroid cancer.

Original languageEnglish
Title of host publicationSurgery of the Thyroid and Parathyroid Glands
PublisherSpringer-Verlag Berlin Heidelberg
Pages235-247
Number of pages13
Volume9783642234590
ISBN (Electronic)9783642234590
ISBN (Print)3642234585, 9783642234583
DOIs
StatePublished - Jul 1 2012

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