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About 65 results

ALLMedicine™ Malignant Atrophic Papulosis Center

Research & Reviews  25 results

A Case of Malignant Atrophic Papulosis With Multiple Complications.
https://doi.org/10.14309/ajg.0000000000001322
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,|

Degos-like lesions as a cutaneous manifestation of cytomegalovirus infection: A rare an...
https://doi.org/10.1111/1346-8138.15717
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...

Degos disease: A radiological-pathological correlation of the neuroradiological aspects...
https://doi.org/10.1016/j.anndiagpath.2020.151545
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 ...

Chronic pleuritis leading to severe pulmonary restriction: a rare complication of Degos...
https://doi.org/10.1136/bcr-2019-232759
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 ...

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News  1 results

Lesions Resembling Malignant Atrophic Papulosis in a Patient With Progressive Systemic Sclerosis
https://www.mdedge.com/dermatology/article/67207/lesions-resembling-malignant-atrophic-papulosis-patient-progressive
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.

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