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Title: [Angioendotheliomatosis proliferans systematizata]. Author: Schley G, Kauffold D, Guse E, Slucka S, Jeschke M. Journal: Hautarzt; 2001 Nov; 52(11):1030-4. PubMed ID: 11757458. Abstract: Angioendotheliomatosis proliferans systematisata comprises two different entities; a malignant and benign (reactive) form. The more common malignant form with a fatal prognosis should be termed intravascular or angiotropic lymphoma and is a multifocal systemic disease, which affects especially the small and middle-sized blood vessels of the skin and central nervous system. Reactive angioendotheliomatosis is a benign disease, often associated with an infectious disease (predominantly with subacute bacterial endocarditis). We report a 38-year-old woman with a reactive angioendotheliomatosis and a 68-year-old man diagnosed as having the rare T-cell type of intravascular lymphoma.[Abstract] [Full Text] [Related] [New Search]