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 language | English |
|---|---|
| Title of host publication | Surgery of the Thyroid and Parathyroid Glands |
| Publisher | Springer-Verlag Berlin Heidelberg |
| Pages | 235-247 |
| Number of pages | 13 |
| Volume | 9783642234590 |
| ISBN (Electronic) | 9783642234590 |
| ISBN (Print) | 3642234585, 9783642234583 |
| DOIs | |
| State | Published - Jul 1 2012 |