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Hashimoto's thyroiditis

Hashimoto's thyroiditis
Synonyms chronic lymphocytic thyroiditis, autoimmune thyroiditis, struma lymphomatosa
Hashimoto thyroiditis - alt -- very low mag.jpg
The thyroid of someone with Hashimoto's thyroiditis as seen with a microscope at low magnification
Classification and external resources
Specialty endocrinology
ICD-10 E06.3
ICD-9-CM 245.2
OMIM 140300
DiseasesDB 5649
eMedicine med/949
Patient UK Hashimoto's thyroiditis
MeSH D050031
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Hashimoto's thyroiditis, also known as chronic lymphocytic thyroiditis, is an autoimmune disease in which the thyroid gland is gradually destroyed. Early on there may be no symptoms. Over time the thyroid may enlarge forming a painless goitre. Some people eventually develop hypothyroidism with its accompanying weight gain, feeling tired, constipation, depression, and general pains. After many years the thyroid typically shrinks in size. Potential complications include thyroid lymphoma.

Hashimoto's thyroiditis is thought to be due to a combination of genetic and environmental factors. Risk factors include a family history of the condition and having another autoimmune disease. Diagnosis is confirmed with blood tests for TSH, T4, and antithyroid antibodies. Other conditions that can produce similar symptoms include Graves’ disease and nontoxic nodular goiter.

Hashimoto's thyroiditis, regardless of whether or not hypothyroidism is present, can be treated with levothyroxine. If hypothyroidism is not present some may recommend no treatment while others may treat to try to reduce the size of the goitre. Those affected should avoid eating large amounts of iodine; however, sufficient iodine is required especially during pregnancy. Surgery is rarely required to treat the goitre.

Hashimoto's thyroiditis affects about 5% of the population at some point in their life. It typically begins between the ages of 30 and 50 and is much more common in women than men. Rates of disease appear to be increasing. It was first described by the Japanese physician Hakaru Hashimoto in 1912. In 1957 it was recognized as an autoimmune disorder.


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