(de Quervain Thyroiditis; Giant Cell Thyroiditis; Granulomatous Thyroiditis)
(See also Overview of Thyroid Function.)
History of an antecedent viral upper respiratory infection is common. Histologic studies show less lymphocytic infiltration of the thyroid than in Hashimoto thyroiditis or silent lymphocytic thyroiditis, but there is characteristic giant cell infiltration, polymorphonuclear lymphocytes, and follicular disruption.
There is pain in the anterior neck and fever. Neck pain characteristically shifts from side to side and may settle in one area, frequently radiating to the jaw and ears. It is often confused with dental pain, pharyngitis, or otitis and is aggravated by swallowing or turning of the head. Symptoms of hyperthyroidism are common early in the disease because of hormone release from the disrupted follicles. There is more lassitude and prostration than in other thyroid disorders. On physical examination, the thyroid is asymmetrically enlarged, firm, and tender.
Diagnosis is primarily clinical, based on finding an enlarged, tender thyroid in patients with the appropriate clinical history. Thyroid testing with TSH and at least a free T4 measurement is usually also done. Radioactive iodine uptake should be measured to confirm the diagnosis.
Laboratory findings early in the disease include an increase in free T4 and triiodothyronine (T3), a marked decrease in TSH and thyroid radioactive iodine uptake (often 0), and a high ESR. After several weeks, the thyroid is depleted of T4 and T3 stores, and transient hypothyroidism develops accompanied by a decrease in free T4 and T3, a rise in TSH, and recovery of thyroid radioactive iodine uptake. Weakly positive thyroid antibodies may be present. Measurement of free T4, T3, and TSH at 2- to 4-week intervals identifies the stages of the disease.
When the diagnosis is uncertain, fine-needle aspiration biopsy is useful. Thyroid ultrasonography with color Doppler shows multiple irregular sonolucent areas and reduced blood flow in contrast with the increased flow of Graves disease.
Subacute thyroiditis is self-limited, generally subsiding in a few months; occasionally, it recurs and may result in permanent hypothyroidism when follicular destruction is extensive.
Discomfort is treated with high doses of aspirin or NSAIDs. In moderately symptomatic cases, corticosteroids (eg, prednisone 15 to 30 mg orally once a day, gradually decreasing the dose over 3 to 4 weeks) eradicate all symptoms within 48 hours.
Bothersome hyperthyroid symptoms may be treated with a short course of a beta-blocker. If hypothyroidism is pronounced or persists, thyroid hormone replacement therapy may be required, rarely permanently.
Manifestations of subacute thyroiditis are usually fever, neck pain, and an enlarged, tender thyroid.
Patients are initially hyperthyroid, with low levels of thyroid-stimulating hormone (TSH) and elevated free thyroxine (T4); they sometimes then become transiently hypothyroid, with high TSH and low free T4.
Treatment is with nonsteroidal anti-inflammatory drugs plus sometimes corticosteroids and/or a beta-blocker.
Drugs Mentioned In This Article
|Drug Name||Select Trade|
|No US brand name|