Screening is a way to evaluate people without symptoms to determine if they are at risk for cancer or have already developed cancer.

Screening involves:

    
  • Assessing your medical history and lifestyle habits that may increase or decrease your risk of thyroid cancer
  • Testing to identify early signs of thyroid cancer
  • Screening Guidelines

    According to the US Preventive Services Task Force, there are no official screening guidelines for thyroid cancer. Testing is only recommended for people who are experiencing symptoms suggestive of thyroid cancer.

    According to the American Cancer Society, all people between the ages of 21 and 40 should have their neck, lymph nodes, and the area directly over their thyroid gland examined (palpated) every year.

    There are some healthcare providers who think that people with a higher-than-normal risk of thyroid cancer should be periodically screened. Factors that lead to a higher-than-normal risk include the following:

        
  • A history of exposure to radiation
  • Family members with either multiple endocrine neoplasia (MEN) associated thyroid cancer or non-MEN associated thyroid cancer
  • If you fit one of these categories, you may be advised to have your blood calcitonin levels measured periodically, as well as undergo annual neck and thyroid palpation.

    If members of your family have a genetic defect (a change or mutation in the RET gene) that increases the risk of medullary thyroid cancer, you should strongly consider having genetic testing done to determine your personal risk and the risk of transmitting this gene to your children. The screening blood tests include: calcitonin and RET proto-oncogene. This type of cancer may arise during childhood and at a very young age. Thus families may wish to openly discuss the risks and benefits of genetic testing to determine the frequency of screening among members.