ALLMedicine™ Degos Disease Center
Research & Reviews 52 results
Clinical and Experimental Dermatology; Narang I, Chohan B et. al.
Jun 30th, 2021 - Degos disease with renal cell carcinoma.|2021|Narang I,Chohan B,Bleiker TO,|
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Orphanet Journal of Rare Diseases; Lu JD, Sachdeva M et. al.
May 8th, 2021 - Degos disease is a rare vascular disorder with a cutaneous-limited form, benign atrophic papulosis (BAP), and a systemic variant, malignant atrophic papulosis (MAP). Despite the poor prognosis of MAP, no study has established features associated w...
Journal of the European Academy of Dermatology and Venere... Kim PJ, Lytvyn Y et. al.
Apr 30th, 2021 - Degos disease (atrophic papulosis) is a rare vasculopathy with cutaneous and systemic manifestations. Although potentially fatal, the characteristics of and treatments for Degos disease variants are not adequately described. We conducted a systema...
International Journal of Dermatology; Stephan C, Kurban M et. al.
Dec 29th, 2020 - Dowling-Degos disease is a rare autosomal dominant genodermatosis. It is characterized by acquired reticulate hyperpigmentation over the flexures, comedone-like follicular papules, and pitted perioral scars that usually develop during adulthood. M...
The Journal of Dermatology; Chieosilapatham P, Prinyaroj N et. al.
Dec 12th, 2020 - Cytomegalovirus causes a myriad of clinical features, potentially affecting any organ system, significantly increasing morbidity and even mortality. Vascular endothelial cell infection by cytomegalovirus has been implicated in the development of v...
News 1 results
Sep 10th, 2015 - The differential diagnosis for a patient with purpuric/necrotic skin lesions should be broad and include vasculitis (eg, inflammatory, antineutrophil cytoplasmic antibody positive, septic), hypercoagulopathy (eg, antiphospholipid syndrome, antith.