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Medullary thyroid carcinoma (MTC) arises from
parafollicular or C cells of the thyroid and
accounts for 5 % to 10 % of all thyroid cancers.
Hereditary MTC represents 20 to 30 % of all
MTC’s. It can be transmitted with an autosomal
dominant pattern either as a single entity, familial
MTC (FMTC), or it can arise as part of a multiple
endocrine neoplasia (MEN) syndrome type 2A or
2B. The identification of hereditary MTC has been
facilitated in recent years by the direct analysis of
the ret proto-oncogene 1,2 .
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