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Hashimoto's thyroiditis

Hashimoto's thyroiditis, the most common form of thyroiditis, is an autoimmune disease where the body's own antibodies fight the cells of the thyroid. Also known as Hashimoto's disease, it is named after the Japanese physician, Hakaru Hashimoto (1881–1934) of the medical school at Kyushu University, who first described it to medicine in 1912. It is four times more common among women than men, and runs in families, with the HLADR5 gene most strongly implicated (conferring a relative risk of 3) in the UK. The genes implicated vary in different ethnic groups. more...

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In many cases, Hashimoto's thyroiditis usually results in hypothyroidism, although in its acute phase, it can cause a transient hyperthyroid state.

Physiologically, antibodies to thyroid peroxidase and/or thyroglobulin cause gradual destruction of follicles in the thyroid gland. Accordingly, the disease can be detected clinically by looking for these antibodies in the blood. It is also characterised by invasion of the thyroid tissue by leukocytes, chiefly T-lymphocytes.

Treatment is by daily thyroxine, with the sodium salt of thyroxine liothyronine given when the need to raise levels of circulating thyroxine is urgent.

Symptoms of Hashimoto's thyroiditis include symptoms of hypothyroidism and a goitre.

In European countries an atrophic form of autoimmune thyroiditis (Ord's thyroiditis) is more common than Hashimoto's thyroiditis.

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Parathyroiditis
From Ear, Nose & Throat Journal, 10/1/05 by Lester D.R. Thompson

Parathyroiditis is a rare and poorly understood condition. Chronic parathyroiditis may occur in patients with hypoparathyroidism, as well as in those with primary chief-cell hyperplasia. Most patients are asymptomatic. Antibodies to parathyroid tissue are seen in only a few cases of parathyroiditis. It is thought that parathyroiditis represents an autoimmune process similar to thyroid gland Hashimoto's disease. The presence of seronegative cases of parathyroiditis does not rule against an autoimmune etiology, because a similar phenomenon is observed in Hashimoto's thyroiditis. Based on this assumption, it is believed that the lymphocytic infiltration is an ongoing destructive process.

Parathyroiditis is characterized by a slightly enlarged gland, although the macroscopic appearance is not specific. Histologically, aggregates of mature lymphocytes are seen infiltrating otherwise normal parathyroid tissue (figure, A). There is often lymphoid follicle formation with prominent germinal centers (figure, B). Plasma cells and fibrosis (often heavy) may be identified, and destruction of the parenchyma has been reported. Atrophy of the residual parathyroid tissue may also be seen. More than one parathyroid gland may be involved, although multifocal disease is seen in the presence of autoimmune disorders, such as Sjogren's disease.

[FIGURE A-B OMITTED]

A chronic inflammatory proliferation may occur as a nonspecific reaction in patients with various infectious disease processes; however, such infiltrates are usually sparse and have a perivascular distribution. Lymphoma involving the parathyroid glands (as part of systemic disease) with distinctive morphologic features has been reported, but it is extremely rare.

The significance of parathyroiditis is unknown, and its management is supportive if clinically necessary.

Suggested reading

Bondeson AG, Bondeson L, Ljungberg O. Chronic parathyroiditis associated with parathyroid hyperplasia and hyperparathyroidism. Am J Surg Pathol 1984:8:211-15.

Lloyd RV. Douglas BR, Young WF, Jr. Endocrine Diseases. Atlas of Nontumor Pathology. 1st series, fascicle I. Washington D.C.: Armed Forces Institute of Pathology, 2002:61-2.

Lester D.R. Thompson, MD

From the Department of Pathology, Woodland Hills Medical Center, Southern California Permanente Medical Group, Woodland Hills, Calif.

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