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Disease summary:
Autoimmune thyroid disorders (AITDs) include Graves disease (GD) and Hashimoto thyroiditis (HT). Both are complex genetic diseases caused by the interplay of several genes with environmental triggers (eg, infection) resulting in disruption of normal thyroid function. AITDs are some of the most common autoimmune disorders and can be associated with other autoimmune diseases. Both are found in a higher prevalence among women with the age of onset most frequently between 30 and 50 years.
Graves disease: Production of thyrotropin (TSH) receptor stimulating antibodies (TRAb) results in overstimulation of the thyroid gland that causes an excessive production and inappropriate release of thyroid hormones resulting in clinical hyperthyroidism, as well as thyroid enlargement (goiter) due to hypertrophy and hyperplasia of thyroid follicles.
Hashimoto disease: Also known as chronic lymphocytic thyroiditis, is the most common cause of hypothyroidism in the industrialized world with a higher prevalence in iodine sufficient areas and among smokers. It is characterized by lymphocytic infiltration of thyroid gland, causing thyroid cell death and resultant hypothyroidism.
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Differential diagnosis:
GD: Subacute thyroiditis, postpartum thyroiditis, silent thyroiditis, toxic multinodular goiter, toxic adenoma, surreptitious ingestion of thyroid hormones, drug-induced thyroiditis (eg, amiodarone, interferon)
HT: Primary myxedema, postpartum thyroiditis, drug-induced hypothyroidism (eg, amiodarone, interferon, lithium)
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Environmental factors:
Iodine, infection, smoking, pregnancy, medications
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Diagnostic Criteria and Clinical Characteristics
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Diagnostic Criteria for AITD
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Diagnosis is based on the presence of primary hyperthyroidism plus at least one of the following: (1) clinically evident GO and/or dermopathy, (2) detectable serum TRAb, or (3) diffuse radioactive iodine uptake on thyroid scan.
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Diagnostic evaluation should include