Thyroid - medullary carcinoma; Cancer - thyroid (medullary carcinoma)
Medullary carcinoma of the thyroid is a malignancy of the thyroid gland arising from the C cell, which secretes the hormone calcitonin.
Causes, incidence, and risk factors
The cause is unknown, but is not thought to be related to radiation therapy, as opposed to other thyroid cancers. Thyroid function tests are usually normal. Risk factors are a family history of multiple endocrine neoplasia (MEN), a prior history of pheochromocytoma, mucosal neuromas, or hyperparathyroidism.
The average age at diagnosis is the mid-40s, except in patients with inherited cancer syndromes, in which the cancer often occurs earlier. Approximately 700 new cases are diagnosed each year in the United States. The condition runs in the family about 20% of the time.
- Firm thyroid mass
- Cough with blood
Signs and tests
- A physical examination reveals enlarged cervical lymph nodes.
- An examination of the thyroid reveals single or multiple nodules.
- A thyroid biopsy shows medullary carcinoma of thyroid cells.
- An ultrasound of the thyroid reveals a nodule.
- A thyroid scan shows a cold nodule.
- The calcitonin level is elevated.
Surgical removal of the thyroid gland, as well as surrounding lymph nodes, is the initial treatment. Chemotherapy and radiation are not very effective.
The risks of surgery include accidental removal of parathyroid glands or nerve tissue of the larynx, which leads to serious complications.
For additional resources, see cancer support group.
The expectation for this type of thyroid cancer varies, depending on the ability of surgery to remove all cancerous tissue. The 10-year survival rate (amount of people who live for at least 10 years after diagnosis) is 70 to 80%.
- Medullary carcinoma invading nearby lymph nodes
- Inadvertent removal of parathyroid glands during surgery
- Metastasis of cancer to blood vessels or other sites
Calling your health care provider
Call for an appointment with your health care provider if symptoms of this disorder develop.
Prevention may not be possible. However, being aware of your risk factors, especially a family history, may allow early diagnosis and treatment.
by Arthur A. Poghosian, M.D.
All ArmMed Media material is provided for information only and is neither advice nor a substitute for proper medical care. Consult a qualified healthcare professional who understands your particular history for individual concerns.