ArticleAnais brasileiros de dermatologia
Acral papular mucinosis: a new case of this rare entity.
Article in Anais brasileiros de dermatologia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- [Flesh-coloured hyperkeratotic papules on the dorsae of the hands].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2020Article
- A rare case of acral persistent papular mucinosis.Clinical case reports · 2020Article
- Lichen myxedematosus: a rare group of cutaneous mucinosis.Anais brasileiros de dermatologia · 2019Review
- Acral persistent papular mucinosis with pruritic skin lesions.Anais brasileiros de dermatologiaArticle
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5 authors.
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Abstract
Acral persistent papular mucinosis (APPM) is a rare subtype of localized lichen myxedematosus. It consists of small papules localized exclusively on the back of the hands, wrists and extensor aspects of distal forearms with no other clinical or laboratory manifestations. The lesions tend to persist and may increase slowly in number. Histologically, hematoxylin-eosin and Alcian blue staining demonstrate mucin accumulation in the upper reticular dermis with separation of collagen fibers as a result of hyaluronic acid deposition. Treatment is rarely necessary due to the absence of symptoms. We present a 27-year-old healthy woman with asymptomatic papules on her upper extremities, which adequately meet clinical and pathological criteria of acral papular mucinosis.
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