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About 119 results

ALLMedicine™ Malignant Atrophic Papulosis Center

Research & Reviews  59 results

Pairing and comparing nine diseases with Degos Disease (Malignant Atrophic Papulosis): ...
https://www.ncbi.nlm.nih.gov/pubmed/19281715
Dermatology Online Journal; Scheinfeld N

Mar 13th, 2009 - Degos disease is a poorly defined condition that encompasses cutaneous and systemic findings that overlap with a large number of other rheumatologic and coagulation disorders. Comparisons are made herein with 9 conditions that share findings and p...

Benign atrophic papulosis (Köhlmeier-Degos disease): the wedge-shaped dermal necrosis c...
https://doi.org/10.1111/jdv.14355
Journal of the European Academy of Dermatology and Venere... Zouboulis CC, Theodoridis A et. al.

May 25th, 2017 - Atrophic papulosis is a rare thrombo-occlusive disease, characterized by the appearance of multiple atrophic porcelain-white skin papules, with a surrounding erythematous rim, which are histologically consisting of wedge-shaped necrosis of the der...

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.

Benign Atrophic Papulosis (Degos Disease) With Lymphocytic Vasculitis and Lichen Sclero...
https://doi.org/10.1097/DAD.0000000000000847
The American Journal of Dermatopathology; Kim E, Motaparthi K

Feb 28th, 2017 - Degos disease manifests as 2 distinct clinical variants, malignant atrophic papulosis and benign atrophic papulosis, which are distinguished by the presence or absence of systemic disease. Both forms feature cutaneous involvement typified by eryth...

Opioid associated intravenous and cutaneous microvascular drug abuse (skin-popping) mas...
https://www.ncbi.nlm.nih.gov/pubmed/26437280
Dermatology Online Journal; Magro CM, Toledo-Garcia A et. al.

Oct 5th, 2015 - In 2012, a nephrologist reported the development of a multiorgan thrombotic syndromic complex resembling thrombotic thrombocytopenic purpura (TTP) in patients who were abusing long acting oxymorphone hydrochloride; all patients had hemolytic anemi...

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Clinicaltrials.gov  59 results

Pairing and comparing nine diseases with Degos Disease (Malignant Atrophic Papulosis): ...
https://www.ncbi.nlm.nih.gov/pubmed/19281715
Dermatology Online Journal; Scheinfeld N

Mar 13th, 2009 - Degos disease is a poorly defined condition that encompasses cutaneous and systemic findings that overlap with a large number of other rheumatologic and coagulation disorders. Comparisons are made herein with 9 conditions that share findings and p...

Benign atrophic papulosis (Köhlmeier-Degos disease): the wedge-shaped dermal necrosis c...
https://doi.org/10.1111/jdv.14355
Journal of the European Academy of Dermatology and Venere... Zouboulis CC, Theodoridis A et. al.

May 25th, 2017 - Atrophic papulosis is a rare thrombo-occlusive disease, characterized by the appearance of multiple atrophic porcelain-white skin papules, with a surrounding erythematous rim, which are histologically consisting of wedge-shaped necrosis of the der...

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.

Benign Atrophic Papulosis (Degos Disease) With Lymphocytic Vasculitis and Lichen Sclero...
https://doi.org/10.1097/DAD.0000000000000847
The American Journal of Dermatopathology; Kim E, Motaparthi K

Feb 28th, 2017 - Degos disease manifests as 2 distinct clinical variants, malignant atrophic papulosis and benign atrophic papulosis, which are distinguished by the presence or absence of systemic disease. Both forms feature cutaneous involvement typified by eryth...

Opioid associated intravenous and cutaneous microvascular drug abuse (skin-popping) mas...
https://www.ncbi.nlm.nih.gov/pubmed/26437280
Dermatology Online Journal; Magro CM, Toledo-Garcia A et. al.

Oct 5th, 2015 - In 2012, a nephrologist reported the development of a multiorgan thrombotic syndromic complex resembling thrombotic thrombocytopenic purpura (TTP) in patients who were abusing long acting oxymorphone hydrochloride; all patients had hemolytic anemi...

see more →

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.

see more →