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About 119 results

ALLMedicine™ Malignant Atrophic Papulosis Center

Research & Reviews  59 results

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 References; Chieosilapatham P, Prinyaroj N et. al.

Dec 11th, 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 8th, 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 10th, 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 ...

Degos Disease
https://emedicine.medscape.com/article/1087180-overview

Dec 9th, 2019 - Background In 1941, in an article entitled "Multiple Hautrekrosen bei Thromboangiitis obliterans," Kohlmeier described a case of a disease that has now been termed malignant atrophic papulosis (MAP) or Degos disease. Degos recognized it as a disti...

Degos Disease 
https://emedicine.medscape.com/article/1087180-print

Dec 9th, 2019 - Background In 1941, in an article entitled "Multiple Hautrekrosen bei Thromboangiitis obliterans," Kohlmeier described a case of a disease that has now been termed malignant atrophic papulosis (MAP) or Degos disease. Degos recognized it as a disti...

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Clinicaltrials.gov  59 results

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 References; Chieosilapatham P, Prinyaroj N et. al.

Dec 11th, 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 8th, 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 10th, 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 ...

Degos Disease
https://emedicine.medscape.com/article/1087180-overview

Dec 9th, 2019 - Background In 1941, in an article entitled "Multiple Hautrekrosen bei Thromboangiitis obliterans," Kohlmeier described a case of a disease that has now been termed malignant atrophic papulosis (MAP) or Degos disease. Degos recognized it as a disti...

Degos Disease 
https://emedicine.medscape.com/article/1087180-print

Dec 9th, 2019 - Background In 1941, in an article entitled "Multiple Hautrekrosen bei Thromboangiitis obliterans," Kohlmeier described a case of a disease that has now been termed malignant atrophic papulosis (MAP) or Degos disease. Degos recognized it as a disti...

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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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