papular mucinosis

Frequently, all three forms are regarded as papular mucinosis.

Another form, acral persistent papular mucinosis is regarded as a separate entity.

Papular mucinosis may be divided into several types or variants:

Papular mucinosis is chronic and may be progressive.

Papular mucinosis affects adults of both sexes equally and appears between ages 30 and 80.

Papular Mucinosis, Dermatology Online Journal Vol.

Self-healing papular mucinosis is a skin condition caused by fibroblasts producing abnormally large amounts of mucopolysaccharides, and may present in adult and juvenile forms.

Localized and disseminated cases are called papular mucinosis or lichen myxedematosus while generalized, confluent papular forms with sclerosis are called scleromyxedema.

Papular mucinosis (also known as "Scleromyxedema," "Generalized lichen myxedematosus," and "Sclerodermoid lichen myxedematosus") is a rare skin disease.

Acral persistent papular mucinosis is a skin condition caused by fibroblasts producing abnormally large amounts of mucopolysaccharides, characterized by bilaterally symmetrical, flesh-colored papules localized to the hands and wrists.

Papular mucinosis of infancy (also known as "Cutaneous mucinosis of infancy") is a skin condition caused by fibroblasts producing abnormally large amounts of mucopolysaccharides, characterized by skin-colored or translucent papules.