Thyroid cancer originates from one of the cells inside the thyroid gland, typically from within a nodule that has formed inside the thyroid.
The cause for most thyroid cancers is not known, not the fault of the patient (e.g. caused by diet, exercise, drinking, smoking, etc.), and not commonly passed down from family members (i.e. occurs sporadically).
- Exceptions include:
- Radiation treatments to the head and neck (particularly in childhood).
- Proximity to radiation (from radioactive fallout – e.g. Chernobyl, or working with radiation or radioactive materials without proper protection).
- Inherited genetically – typically multiple 1st degree relatives with thyroid cancer.
- Accounts for 3 – 9% of Well Differentiated Thyroid Cancers.
- Associated with rare genetic syndromes:
- PTEN hamartoma tumor syndrome (Cowden’s disease), familial adenomatous polyposis (FAP), Carney complex, multiple endocrine neoplasia (MEN 2A and 2B), Werner syndrome / progeria.
Most thyroid cancers are asymptomatic and discovered on routine physical exams (mass in the neck) or incidentally on imaging (e.g. CT, MRI, or ultrasound of the neck / chest).
- The presence of thyroid cancer does not affect the function of the thyroid.
- Therefore, thyroid cancers cannot be diagnosed or detected on thyroid hormone lab tests.