Papular mucinosis

From WikiMD's Wellness Encyclopedia

(Redirected from Arndt-Gottron disease)

Papular mucinosis (also known as Lichen myxedematosus) is a rare skin disorder characterized by the deposition of mucin in the skin. It is a form of cutaneous mucinosis, a group of conditions that involve the accumulation of mucin in the skin.

Symptoms[edit | edit source]

The primary symptom of papular mucinosis is the presence of small, firm, waxy papules on the skin. These papules are typically skin-colored or slightly red, and they may be found anywhere on the body, although they are most commonly seen on the arms, legs, and trunk. In some cases, the papules may coalesce to form larger plaques.

Causes[edit | edit source]

The exact cause of papular mucinosis is unknown. However, it is believed to be related to an overproduction of hyaluronic acid, a type of mucin, in the skin. This overproduction may be triggered by a variety of factors, including certain medications, autoimmune diseases, and genetic predisposition.

Diagnosis[edit | edit source]

Diagnosis of papular mucinosis is typically made based on the characteristic appearance of the skin lesions. A skin biopsy may also be performed to confirm the diagnosis and rule out other conditions. The biopsy will typically show an accumulation of mucin in the dermis, the middle layer of the skin.

Treatment[edit | edit source]

Treatment for papular mucinosis is primarily aimed at managing the symptoms and improving the appearance of the skin. This may include the use of topical corticosteroids, retinoids, or other medications to reduce inflammation and slow the production of mucin. In severe cases, systemic therapy with medications such as methotrexate or cyclophosphamide may be necessary.

See also[edit | edit source]

References[edit | edit source]

Papular mucinosis Resources
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Contributors: Prab R. Tumpati, MD