ALLMedicine™ Malignant Atrophic Papulosis Center
Research & Reviews 25 results
The American Journal of Gastroenterology; Wang H, Zhang X
Jun 3rd, 2021 - A Case of Malignant Atrophic Papulosis With Multiple Complications.|2021|Wang H,Zhang X,|
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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...
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...
Annals of Diagnostic Pathology; Moran EJ, Lapin WB et. al.
Jun 9th, 2020 - Malignant atrophic papulosis (Degos disease) is an unusual thrombotic microangiopathy of uncertain etiology. The disease characteristically involves the skin and internal organs, with nervous system involvement more common in children. We present ...
BMJ Case Reports; Saha BK, Beegle S
Dec 11th, 2019 - This case demonstrates chronic fibrosing pleuritis, as a rare pulmonary aetiology for mortality in patients with Degos disease or malignant atrophic papulosis (MAP). Knowledge of this unusual complication will help physicians identify this entity ...
News 1 results
Liu CM, Harris RM et. al.
Malignant atrophic papulosis (MAP), or Degos syndrome, is a rare disorder of unknown etiology. It is characterized by a deep subcutaneous vasculopathy resulting in atrophic, porcelain-white papules.