ALLMedicine™ Degos Disease Center
Research & Reviews 69 results
Journal of the European Academy of Dermatology and Venere... Zouboulis CC, Theodoridis A et. al.
Jun 25th, 2022 - Although the merely cutaneous, benign form of the extremely rare disease atrophic papulosis (Köhlmeier-Degos disease) may occasionally develop into the systemic, malignant form with time, it is unclear whether it exhibits any systemic characterist...
Journal of the European Academy of Dermatology and Venere... Kaleta KP, Jarienė V et. al.
May 26th, 2022 - Atrophic papulosis is a very rare vascular disease of unknown pathogenesis, mostly described by case reports. To assess demographic data and prognosis in patients with atrophic papulosis. A single-centre study was performed on a series of 105 pati...
Annals of Diagnostic Pathology; Magro C, Shapiro L
May 20th, 2022 - Kohlmeier-Degos Disease is a unique thrombotic microvascular and arteriopathic vasculopathy that is highly selective in the organs it targets. It invariably involves the skin and can be a purely cutaneous process. It affects both the microvasculat...
Orphanet Journal of Rare Diseases; Sattler SS, Magro CM et. al.
Apr 22nd, 2022 - Kohlmeier-Degos (K-D) disease is a rare obliterative vasculopathy that can present as a benign cutaneous form or with potentially malignant systemic involvement. The gastrointestinal tract is most frequently involved in systemic disease and mortal...
Journal of Cardiothoracic Surgery; Tadokoro Y, Kitamura T et. al.
Apr 3rd, 2022 - Degos disease, also known as malignant atrophic papulosis, is characterised by cutaneous manifestations due to chronic thrombo-obliterative vasculopathy. There have been reports of the rare late-onset Degos disease complicated by constrictive peri...
News 3 results
Spyros M. Siscos, MD, Jace Rickstrew, MD et. al.
Jul 7th, 2021 - The Diagnosis: Dowling-Degos Disease Histopathology demonstrated elongation of the epidermal rete ridges with increased basal pigmentation, suprapapillary epithelial thinning, dermal melanophages, and a mild lymphocytic infiltrate (Figure). Given.
Santana D. VanDyke, MD, Darren J. Guffey, MD et. al.
Jun 14th, 2021 - The Diagnosis: Degos Disease The pathophysiology of Degos disease (malignant atrophic papulosis) is unknown. 1 Histopathology demonstrates a wedge-shaped area of dermal necrosis with edema and mucin deposition extending from the papillary dermis to.
Shen Z, Chen L et. al.
Feb 1st, 2011 - No abstract available.