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Malignant Atrophic PapulosisLegal notice  


Other terms
Atrophic Papuloses, Malignant,Atrophic Papulosis, Malignant,Malignant Atrophic Papuloses,Papuloses, Malignant Atrophic,Papulosis, Malignant Atrophic,Erythrokeratoderma en cocardes,Degos Syndrome,Syndrome, Degos,Degos Disease,Disease, Degos,Kohlmeier-Degos Disease,Disease, Kohlmeier-Degos,Kohlmeier Degos Disease

Description
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.



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Legal notice
The U.S. National Library of Medicine is the creator, maintainer, and provider of the data above.
The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
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