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Medullary thyroid carcinoma

Introduction: Medullary thyroid carcinoma

Description of Medullary thyroid carcinoma

Medullary thyroid carcinoma: This carcinoma comprises less than 10% of all thyroid cancers. This specific type as significant diagnostic importance because of its aggressive nature and its close association with multiple endocrine neoplasia syndromes. Approximately 10% to 20% of medullary thyroid carcinoma is familial. Patients usually present with a thyroid nodule that is painless and firm. In the majority of cases nodal metastases is present at diagnosis. Surgery is the preferred treatment for both primary therapy and recurrent cases. It is generally not very sensitive to radiation and almost unresponsive to chemotherapy. - 2002
Source: Diseases Database

Medullary thyroid carcinoma: two types are found, familial and sporadic; if familial, the carcinoma is bilateral and may be associated with other benign or malignant endocrine organ tumors; if sporadic, it is unilateral; thyroidectomy and radiation therapy are treatments of choice.
Source: CRISP

Medullary thyroid carcinoma: Related Topics

These medical condition or symptom topics may be relevant to medical information for Medullary thyroid carcinoma:

Terms associated with Medullary thyroid carcinoma:

Broader terms for Medullary thyroid carcinoma

Source - CRISP

External links related to: Medullary thyroid carcinoma

Source: Diseases Database

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