Medullary thyroid cancer is the third most common type of thyroid cancer. This article will discuss common medullary thyroid cancer symptoms and treatments as well as medullary thyroid cancer diagnosis and prognosis. Read ourIntroduction to Thyroid Cancer article for a general overview of the different types of thyroid cancer.
You can also visit our Patient Guide to Thyroid Cancer to learn about thyroid cancer diagnosis and treatments.
Medullary tumors are the third most common of all thyroid cancers. They make up about 3% of all thyroid cancer cases.
But what are some common medullary thyroid cancer symptoms? Unlike papillary thyroid cancer and follicular thyroid cancer that arise from thyroid hormone producing cells, medullary thyroid cancer originates from the parafollicular cells (also called C cells) of the thyroid.
These C cells make a different hormone called calcitonin, which has nothing to do with the control of metabolism the way thyroid hormone does. As you will see below, the production of this hormone can be measured after an operation to determine if the cancer is still present and if it is growing.
This cancer has a much lower cure rate than does the well-differentiated thyroid cancers (papillary and follicular), but cure rates are higher than they are for anaplastic thyroid cancer. Overall, 10-year survival rates are 90% when all the disease is confined to the thyroid gland; 70% with spread to cervical lymph nodes; and 20% when spread to distant sites.
Characteristics of Medullary Thyroid Cancer
- Occurs in 4 clinical settings (see below) and can be associated with other endocrine tumors
- More common in females than males (except for inherited cancers)
- Regional metastases (spread to neck lymph nodes) occurs early in the disease
- Spread to distant organs (metastasis) occurs late and can be to the liver, bone, brain, and adrenal medulla
- Not associated with radiation exposure
- Usually originates in the upper central lobe of the thyroid
- Poor prognostic factors include mean older than 50 years old, distant spread (metastases), and when seen in patients with other endocrine tumors due to MEN II-B syndrome.
- Residual disease (following surgery) or recurrence can be detected by measuring calcitonin (a hormone that should be measured every 4 months for the first few years and then every 6 months for the rest of your life)
Medullary Thyroid Cancer Occurs in 4 Clinical Settings
- Sporadic: Accounts for 80% of all cases of medullary thyroid cancer. They are typically unilateral and there are not associated endocrinopathies (not associated with disease in other endocrine glands). Peak onset is between 40 and 60 years old. Females out number males by a 3:2 ratio. One third will present with intractable diarrhea. Diarrhea is caused by increased gastrointestinal secretion and hypermotility due to the hormones secreted by the tumor (calcitonin, prostaglandins, serotonin, or VIP).
- MEN II-A (Sipple Syndrome): Multiple endocrine neoplasia syndromes (abbreviated as “MEN”) are a group of endocrine disorders that occur together in the same patient and typically are seen in families because they are inherited. “Syndromes” are medical conditions that occur in groups of 3.Sipple syndrome has 1) bilateral medullary carcinoma or C cell hyperplasia, 2) pheochromocytoma, and 3)hyperparathyroidism.This syndrome is inherited and is due to a defect of a gene (DNA) that helps control the normal growth of endocrine tissues. This inherited syndrome is passed on to all children who get the gene (inherited in an autosomal dominant fashion), which theoretically, would be 50% of all offspring of a person with this defective gene. Because of this, males and females are equally affected. Peak incidence of medullary carcinoma in these patients is in the 30s.
- MEN II-B. With this syndrome, patients may also have 1) medullary carcinoma and 2) pheochromocytoma, but only rarely will they have hyperparathyroidism. Instead these patients have 3) an unusual appearance that is characterized by mucosal ganglioneuromas (tumors in the mouth) and a Marfanoid habitus.Inheritance is autosomal dominant as in MEN II-A, or it can occur sporadically (without being inherited). MEN II-B patients usually get medullary carcinoma in their 30s, and males and females are equally effected. As with MEN II-A, pheochromocytomas must be detected prior to any operation. The idea here is to remove the pheochromocytoma first to remove the risk of severe hypertensive episodes while the thyroid or parathyroid is being operated on.
- Inherited medullary carcinoma without associated endocrinopathies. This form of medullary carcinoma is the least aggressive. As with other types of thyroid cancers, the peak incidence is between 40 and 50 years old.