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[The benign form of malignant atrophic papulosis (Köhlmeier-Degos disease)]. 2018

Carolin Haas, and Tanja von Braunmühl, and Thomas Herzinger
Klinik und Poliklinik für Dermatologie und Allergologie, Ludwig-Maximilians-Universität München, Frauenlobstr. 9-11, 80337, München, Deutschland. Carolin.Blatner@med.uni-muenchen.de.

UI MeSH Term Description Entries
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D012867 Skin The outer covering of the body that protects it from the environment. It is composed of the DERMIS and the EPIDERMIS.
D054853 Malignant Atrophic Papulosis Variously described as a vasculopathy, endovasculitis, or occlusive arteriopathy, this condition occurs in a benign cutaneous form and a lethal multiorgan systemic variant. It is characterized by a narrowing and occlusion of the lumen of small to medium-sized blood vessels, leading to ischemia and infarction in the involved organ systems. The etiology and pathophysiology are unknown. Degos Disease,Kohlmeier-Degos Disease,Degos Syndrome,Degos's Malignant Atrophic Papulosis,Erythrokeratoderma en cocardes,Papulosis, Malignant Atrophic,Atrophic Papuloses, Malignant,Atrophic Papulosis, Malignant,Disease, Degos,Disease, Kohlmeier-Degos,Malignant Atrophic Papuloses,Papuloses, Malignant Atrophic,Syndrome, Degos

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