Thyroid Cancer pp 239-249 | Cite as

Diagnosis of Medullary Thyroid Cancer

Abstract

Medullary thyroid carcinoma (MTC) is a rare calcitonin (CT)-secreting tumor of the parafollicular or C cells of the thyroid. As the C cells originate from the embryonic neural crest, MTC often has the clinical and histological features of neuroendocrine tumors. It accounts for 8%–12% of all thyroid carcinomas and occurs in both sporadic and hereditary forms. The discovery of an MTC in a patient has several diagnostic implications involving a specific strategy: preoperative evaluation of the extent of the disease, classification of MTC as sporadic or hereditary by DNA testing, and screening for associated endocrinopathies in hereditary MTC.

Keywords

Codon Cysteine Diarrhea Catecholamine Statin 

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© Springer-Verlag Berlin Heidelberg 2001

Authors and Affiliations

  • F. Raue

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