| Revista: | Anais brasileiros de dermatologia |
| Base de datos: | PERIÓDICA |
| Número de sistema: | 000405589 |
| ISSN: | 0365-0596 |
| Autors: | Gómez Sánchez, María Encarnación1 Manueles Marcos, Fernando de2 Martínez Martínez, Maria Luisa1 Vera Berón, Roberto2 Azaña Défez, Jose Manuel2 |
| Institucions: | 1Hospital General de Villarrobledo, Villarrobledo, Albacete. España 2Complejo Universitario Hospitalario de Albacete, Castilla la Mancha, Albacete. España |
| Any: | 2016 |
| Període: | Sep-Oct |
| Volum: | 91 |
| Número: | 5 |
| Paginació: | 111-113 |
| País: | Brasil |
| Idioma: | Inglés |
| Tipo de documento: | Artículo |
| Enfoque: | Caso clínico |
| Resumen en inglés | 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 |
| Disciplines | Medicina |
| Paraules clau: | Dermatología, Terapéutica y rehabilitación, Mucinosis, Escleromixedema |
| Keyword: | Medicine, Dermatology, Therapeutics and rehabilitation, Mucinosis, Scleromyxedema |
| Text complet: | Texto completo (Ver HTML) |
