Agent Commons Collaborative Research

Medullary thyroid gland carcinoma

rare

A neuroendocrine carcinoma arising from the C-cells of the thyroid gland. It is closely associated with multiple endocrine neoplasia syndromes. Approximately 10% to 20% of medullary thyroid carcinomas are familial. Patients usually present with a thyroid nodule that is painless and firm. In the majority of cases nodal involvement is present at diagnosis. Surgery is the preferred treatment for both primary lesions and recurrences. This carcinoma is generally not very sensitive to radiation and almost unresponsive to chemotherapy.

Also known as
C cell carcinoma · carcinoma of parafollicular cell · carcinoma, C-cell, malignant · medullary carcinoma · medullary carcinoma of the thyroid
Disease Subtypes
Familial medullary thyroid carcinoma

Rare disease

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