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Thyrotoxicosis Imaging


The term thyrotoxicosis refers to the hypermetabolic clinical syndrome resulting from serum elevations in thyroid hormone levels, specifically free thyroxine (T4) and/or triiodothyronine (T3).

According to the American Thyroid Association (ATA), thyrotoxicosis can occur in the following situations

If the thyroid is excessively stimulated by trophic factors.

If constitutive activation of thyroid hormone synthesis and secretion occurs, leading to autonomous release of excess thyroid hormone.

If thyroid stores of preformed hormone are passively released in excessive amounts owing to autoimmune, infectious, chemical, or mechanical insult.

If there is exposure to extrathyroidal sources of thyroid hormone, which may be either endogenous (struma ovarii, metastatic differentiated thyroid cancer) or exogenous (factitious thyrotoxicosis).

Thyroid hormone homeostasis is illustrated in the image below.

Illustration of the negative feedback loop causing

Illustration of the negative feedback loop causing homeostasis of thyroid hormone levels. A decrease in blood thyroid hormone triiodothyronine (T3)/thyroxine (T4) levels results in the inhibition of thyrotropin-releasing hormone and thyrotropin production. The released thyrotropin stimulates synthesis and release of T3/T4 by the thyroid, which in turn tends to inhibit further thyrotropin release. THS is thyrotropin. TRH is thyrotropin-releasing hormone.

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Neoplasms leading to thyrotoxicosis include autonomously functioning toxic nodules and toxic, multinodular goiters (TMNGs).

Infections that can produce thyrotoxicosis include subacute thyroiditis (SAT) and, very rarely, acute suppurative thyroiditis.

Hyperthyroidism is a type of thyrotoxicosis in which accelerated thyroid hormone biosynthesis and secretion by the thyroid gland produce thyrotoxicosis. However, hyperthyroidism and thyrotoxicosis are not synonymous.
This is because, although many patients have thyrotoxicosis caused by hyperthyroidism, other patients may have thyrotoxicosis resulting from inflammation of the thyroid gland, which causes the release of stored thyroid hormone but not accelerated synthesis, or they may have thyrotoxicosis, which is caused by ingestion of exogenous thyroid hormone.

Differentiating between thyrotoxicosis caused by hyperthyroidism and thyrotoxicosis not caused by hyperthyroidism is important, because disease management and therapy differ for each form. Thyroid imaging and radiotracer thyroid uptake measurements, combined with serologic data, enable specific diagnosis and appropriate patient treatment.

The common causes of thyrotoxicosis have different pathophysiologic features and include autoimmune diseases, functioning thyroid adenomas, and infections.

Autoimmune diseases resulting in thyrotoxicosis include the following:

Graves disease (the most common cause of hyperthyroidism; see the images below)

Lymphocytic thyroiditis with hyperthyroidism (ie, silent thyroiditis)

Postpartum thyrotoxicosis (PPT)

Iodine-123 thyroid scan in a patient with Graves d

Iodine-123 thyroid scan in a patient with Graves disease: Tracer uptake is uniform throughout the gland. The 5-hour iodine uptake was high at 53%.

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Iodine-123 thyroid scan in a patient with Graves d

Iodine-123 thyroid scan in a patient with Graves disease. The 5-hour iodine uptake was elevated at 29%. Note the high level of iodine concentration near the thyroid. Also note the pyramidal lobe, which often is visualized in a hyperstimulated gland. The cold nodule in the right lobe must be addressed in the same way that a solitary cold nodule in a patient without Graves disease is evaluated. Fine-needle aspiration of the nodule prior to iodine-131 treatment did not reveal a carcinoma.

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Neoplasms that cause thyrotoxicosis include autonomously functioning toxic nodules and TMNGs (see the images below); infections that lead to the condition include subacute thyroiditis (SAT) and, very rarely, acute suppurative thyroiditis.

Iodine-123 scan in a patient with a palpable nodul

Iodine-123 scan in a patient with a palpable nodule in the right neck, a low serum level for thyrotropin, and a slightly elevated serum level of free triiodothyronine. The autonomously functioning nodule only partially suppresses uptake in the remainder of the gland. The 5-hour iodine uptake was mildly elevated at 22%.

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Scan in a patient with a toxic, multinodular goite

Scan in a patient with a toxic, multinodular goiter: The 5-hour iodine uptake was elevated at 28%. Note the multiple foci of variably increased tracer uptake.

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The assessment of thyroid blood flow by color-flow Doppler ultrasonography is valuable in the differentiation of destructive thyrotoxicosis from Graves disease, according to a study by Kumar et al. The study was carried out in 65 patients. Destructive thyrotoxicosis was present in 31 patients; the remaining patients had Graves disease. Color-flow Doppler ultrasonography parameters correlated significantly with pertechnetate scan results, demonstrating a comparable sensitivity of 96% and a specificity of 95%.

Phillips and Hennessey noted that, although radioactive iodine is often useful in the diagnosis and treatment of thyrotoxicosis, such tests cannot be performed in many patients because of recent use of iodinated contrast for other diagnostic studies, such as CT scanning. In their study, the investigators found that 45% of patients with newly diagnosed thyrotoxicosis had received iodinated contrast within 2 weeks before endocrinology evaluation; 43 had received iodine for CT and the other 2 for angiography. Only 1 patient required emergent treatment of a condition diagnosed by CT before further diagnostic studies could have been performed.

Donkol et al concluded that color Doppler flow of the inferior thyroid artery was useful in the differential diagnosis of thyrotoxicosis, particularly when a patient has a contraindication of thyroid scintigraphy by radioactive material.

Preferred examination

The diagnosis of thyrotoxicosis is predominately based on laboratory results, including an elevated free T3/T4 level and suppressed thyrotropin level; however, the clinical examination may reveal the etiology. If the thyroid gland is normal or diffusely enlarged on physical examination, the most likely diagnosis is Graves disease.

If one or more thyroid nodules are palpated, the patient probably has an autonomously functioning thyroid nodule (AFTN) or a TMNG. If the thyroid gland is markedly tender, subacute thyroiditis is likely. However, silent thyroiditis is almost always in the differential diagnosis with Graves disease. In addition, some patients with silent thyroiditis may have a tender thyroid gland, and some patients with subacute thyroiditis have only mild thyroid tenderness.

As a result of the clinical overlap, knowledge of thyroid iodine uptake is necessary for specific diagnosis and appropriate therapy in most patients. Also, thyroid radionuclide scintigraphy can help to distinguish Graves disease from a toxic nodule and a TMNG.

Thyroid uptake testing, thyroid scintigraphy, and thyroid ultrasonography are not the primary testing modalities for the diagnosis of thyrotoxicosis, but their findings can be critical in the differential diagnosis of the disease and in selecting treatment once thyrotoxicosis is established with serologic test results.

The ATA notes in its guidelines that ultrasonography with color flow Doppler can distinguish thyroid hyperactivity (increased flow) from destructive thyroiditis and may be particularly useful when radioactive iodine is contraindicated, such as during pregnancy or breastfeeding.

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