Pretibial myxoedema is a form of diffusemucinosis in which there is an accumulation of excess glycosaminoglycans in the dermis and subcutis of the skin. Glycosaminoglycans, also called mucopolysaccharides, are complex carbohydrates that are important for tissue hydration and lubrication. The main glycosaminoglycan in pretibial myxoedema is hyaluronic acid, which is made by cells called fibroblasts.
Pretibial myxoedema is also known as localised myxoedema, thyroid dermopathy, and infiltrative dermopathy.
It is most commonly seen on the shins (pretibial areas) and is characterised by swelling and lumpiness of the lower legs.
What causes pretibial myxoedema?
The exact mechanism for the deposition of glycosaminoglycans in the skin of the lower legs is uncertain.
Pretibial myxoedema is likely to be due to a combination of the following causes.
An immunological process in which thyroid stimulating hormone receptor (TSH-R) antibodies bind to and stimulate fibroblasts to increase glycosaminoglycan production.
A cellular process in which fibroblasts are activated indirectly through sensitised T lymphocytes (immune cells). T cells sensitised to a common antigen (likely TSH-R antibodies) could infiltratedermal tissue and release cytokines (cellular messenger proteins), which activate dermal fibroblasts to produce glycosaminoglycans.
A mechanical process, where myxoedema accumulates in areas of trauma, after prolonged standing, and in dependent sites. This theory may explain why it occurs in the pretibial area. Dependent swelling could result in pooling of immune cells and proteins, increasing the disease effects.
Who gets pretibial myxoedema?
Pretibial myxoedema is nearly always associated with Graves disease. Graves disease is an autoimmune disorder that affects the thyroidgland in which there are antibodies to TSH-R activate the receptor, often causing an increase in circulating thyroid hormone. This is hyperthyroidism or thyrotoxicosis. Symptoms of thyrotoxicosis include weight loss, palpitations, sweating (hyperhidrosis), and tremors
The classic triad of signs of Graves disease is:
Pretibial myxoedema
Ophthalmopathy (prominent eyes due to deposition of myxoedema behind the orbit)
Acropachy (swelling of distaldigits with overgrown nail plates that may lift off the nail bed; similar to clubbing)
Pretibial myxoedema:
Affects 0.5–4.3% of patients with Graves disease; it is seen in up to 13% in those with severe eye disease
Has also been seen in patients with Hashimoto thyroiditis, primaryhypothyroidism (underactive thyroid), and euthyroidism (normal thyroid function)
Is associated with high serum concentrations of TSH-R antibodies
Is most common in people between the ages of 40 and 60
More commonly affects females, with a female:male ratio of 3.5:1.
Pretibial myxoedema
Thyroid ophthalmopathy
Thyroid acropachy
What are the clinical features of pretibial myxoedema?
Pretibial myxoedema can appear before, during, or after the thyrotoxic state. It is not related to thyroid function. It is generally seen 12–24 months after diagnosis.
It is most commonly found on the pretibial areas, the dorsum of the feet, or in sites of prior trauma.
It is usually asymptomatic and more of a cosmetic concern, but can be itchy or sore.
Early lesions are bilateral, firm, non-pitting, asymmetricalplaques or nodules; they may coalesce to form scaly, thickened and hardened skin areas.
Hair follicles are often prominent giving a peau d'orange (orange peel) texture.
The overlying skin may be discoloured, in colours that range from a violet tinge to a slightly pigmented yellow-brown
There may be localised hyperhidrosis (increased sweating) and/or hypertrichosis (increased hair growth) over the affected skin.
The types of pretibial myxoedema can include the following.
Diffuse, non-pitting oedema (swelling) — the most common form
Plaque form — raised plaques on a background of non-pitting oedema
Nodular form — sharply circumscribed tubular or nodular lesions
Elephantiasic form — nodular lesions with pronounced lymphoedema (swelling due to accumulation of lymphatic tissue fluid). Lesions may coalesce to give the entire extremity an enlarged, warty appearance. This form is rare.
How is pretibial myxoedema diagnosed?
Diagnosis of pretibial myxoedema is made by taking a history and finding characteristic clinical appearance on examination of the patient.
Skin biopsy is rarely necessary for diagnosis, especially if there is a history of hyperthyroidism, or Graves ophthalmopathy.
If a biopsy is done, histopathology typically shows deposition of mucin (glycosaminoglycans) throughout the dermis and subcutis.
Histopathology of pretibial myxoedema
H&E stain
Positive mucin stain
Deposited mucin promotes dermal oedema by promoting the retention of fluid in the skin. This results in compression/occlusion of small peripherallymphatics and lymphoedema.
The biopsy also shows attenuation of collagen fibres; they may be frayed, fragmented and widely separated. Stellate (star-shaped) fibroblasts are often observed, but the number of fibroblasts remains normal. Often a mild, superficial lymphocytic infiltrate around blood vessels is seen, and the overlying epidermis may show hyperkeratosis (increased scale).
What is the treatment for pretibial myxoedema?
Pretibial myxoedema is often asymptomatic and mild, and may require no treatment at all.
If symptomatic, treatment options include:
Minimisation of risk factors
Avoid tobacco
Reduce weight
Normalise thyroid function
Compression stockings, which can be worn to improve lymphoedema
Mid to high potency topical corticosteroid, which are usually recommended under occlusion (eg, plastic cling-film wrap) nightly or every other night to enhance effect.
Other therapies reported to be successful include:
Surgical excision has been successful in case reports, but it is generally not recommended due to the risk of pretibial myxoedema developing in injured skin.
What is the prognosis for pretibial myxoedema?
The prognosis is generally quite good. Most patients with asymptomatic pretibial myxoedema do not require treatment or follow-up.
The myxoedema clears up completely in the majority of patients with mild disease.
Even with more severe disease, it resolves in more than half of patients after several years. The elephantiasic form is the most difficult to treat, and is the least likely to clear up.
The likelihood of remission depends on the severity of the initial disease rather than its treatment.
References
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