1.
Indian J Dermatol Venereol Leprol
;
2019 Sep; 85(5): 559-564
Article
| IMSEAR
| ID: sea-192513
2.
An. bras. dermatol
;
90(2): 283-284, Mar-Apr/2015. graf
Article
Dans Anglais
| LILACS
| ID: lil-741079
Sujets)
Animaux , Humains , Souris , Activation des macrophages/immunologie , Macrophages/immunologie , Terminologie comme sujet , Recommandations comme sujet , Facteur de stimulation des colonies de granulocytes et de macrophages/immunologie , Facteur de stimulation des colonies de macrophages/immunologie , Recherche
3.
An. bras. dermatol
;
89(3): 521-522, May-Jun/2014. graf
Article
Dans Anglais
| LILACS
| ID: lil-711606
Résumé
Degos disease, also known as malignant atrophic papulosis, is a rare occlusive vasculopathy of unknown etiology characterized by infarcts in the dermis, gastrointestinal tract, central nervous system, and other organs. It is characterized by papules, which become umbilicated and evolve with a depressed porcelain-white central area, with an erythematous halo with telangiectasias. Histological findings include wedge-shaped dermoepidermal necrosis and blood vessel thrombosis. Approximately 50-60% of patients with systemic symptoms die within 2-3 years, most due to gastrointestinal perforation. We report a typical case, with lethal outcome, in a 45-year-old woman.