Accuracy of FDG-PET Scanning to Diagnose Malignant Thyroid Nodules

Inclusion Criteria

• •Thyroid nodule must be palpable on physical examination or have a minimum size of 1 cm in diameter by ultrasonography, CT or MRI. The minimum size criterion was established to address the spatial resolution limitations of PET/CT imaging.
• •Scheduled for surgical excision of thyroid nodules within 3 months of the date of the FDG-PET/CT scan.
• •Ability to tolerate lying supine for a FDG-PET/CT examination.
• •Age \>/= 18 and \</= 105 (This disease is rare in children and therefore the study will be limited to adults.)
• •Willing to participate in all aspects of the study (patient may opt out of the tissue collection portion.)
• •Patient must be euthyroid with a serum TSH or a free T4 level within the institutional upper and lower limits of normal, measured within 6 months of registration. NOTE: mild deviations from the institutional normal limits may be considered acceptable if the patient has achieved a clinically euthyroid state with medication at a stable dose for \>3 months, and the TSH is considered to be at target by the patient's treating physician. In patients with hyperthyroidism requiring treatment, this euthyroid state may be achieved with administration of a thionamide such as propylthiouracil prior to FDG-PET/CT exam. Patients with hyperthyroid inflammatory conditions such as thyroiditis and toxic multinodular goiter often exhibit increased glucose uptake resulting in diffuse uptake of FDG which may obscure visualization of a thyroid tumor.
• •If female, patient must have a negative pregnancy test at the time of registration, be post-menopausal (with no period in the last twelve months), have had a tubal ligation at least twelve months ago, or have had a hysterectomy.
• •In patients with multinodular disease and a dominant nodule, the nuclear medicine physician responsible for FDG-PET/CT scan interpretation must determine whether the indeterminate nodule can be discriminated on FDG-PET/CT imaging prior to enrollment.
• •A signed and dated written informed consent obtained from the patient or the patient's legally acceptable representative prior to study participation.