Degos' disease, otherwise known as "malignant atrophic papulosis," is a rare condition characterized by typical cutaneous lesions. Its involvement of the gastrointestinal (GI) tract is usually associated with a poor prognosis. We report a case of Degos' disease with GI involvement, which ultimately caused peritonitis, sepsis, and death, despite all treatment measures. A 59-year old woman was admitted to our hospital with acute generalized abdominal pain. The patient had presented initially with multiple skin lesions 2 years earlier, and even with surgery for small-bowel perforation 10 months before this admission, Degos' disease had not been diagnosed. Explorative laparotomy revealed multifocal, ischemic changes in the small bowel with perf...
Copyright © 2011 Jakob Burcharth et al. This is an open access article distributed under the Creativ...
Abstract Degos ' disease (malignant atrophic papulosis) is an occlusive arteriopathy involving ...
A case of acute abdomen disease caused by abdominal angiostrongyliasis is reported. A 42-year-old ot...
Degos disease, also known as malignant atrophic papulosis, is a rare occlusive vasculopathy of unkno...
We report the case of a 20-year-old woman with one-year history of asymptomatic pink papules on the ...
Atrophic papulosis (Kohlmeier\u2013Degos disease or Degos disease) is a rare occlusive arteriopathy ...
Background: Degos disease is a very rare syndrome with a rare type of multisystem vasculopathy of un...
Degos` disease or malignant atrophic papulosis is a rare vasculopathy characterized by the presence ...
No abstract.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/34313/1/20393_ftp.pd
A 30-year-old woman was referred to our unit because of the presence of erythematous papules that ha...
Degos' disease (DD) also known as malignant atrophic papulosis is considered to be a disorder of abn...
Abstract Background Degos disease is a rare vascular ...
Degos\u27 disease or malignant atrophic papulosis is a rare disseminated occlusive vasculopathy affe...
Objective. Involvement of the gastrointestinal (GI) tract is a rare complication of granulomatosis w...
Malignant atrophic papulosis (MAP) is a rare, obliterating vasculopathy affecting multiple systems, ...
Copyright © 2011 Jakob Burcharth et al. This is an open access article distributed under the Creativ...
Abstract Degos ' disease (malignant atrophic papulosis) is an occlusive arteriopathy involving ...
A case of acute abdomen disease caused by abdominal angiostrongyliasis is reported. A 42-year-old ot...
Degos disease, also known as malignant atrophic papulosis, is a rare occlusive vasculopathy of unkno...
We report the case of a 20-year-old woman with one-year history of asymptomatic pink papules on the ...
Atrophic papulosis (Kohlmeier\u2013Degos disease or Degos disease) is a rare occlusive arteriopathy ...
Background: Degos disease is a very rare syndrome with a rare type of multisystem vasculopathy of un...
Degos` disease or malignant atrophic papulosis is a rare vasculopathy characterized by the presence ...
No abstract.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/34313/1/20393_ftp.pd
A 30-year-old woman was referred to our unit because of the presence of erythematous papules that ha...
Degos' disease (DD) also known as malignant atrophic papulosis is considered to be a disorder of abn...
Abstract Background Degos disease is a rare vascular ...
Degos\u27 disease or malignant atrophic papulosis is a rare disseminated occlusive vasculopathy affe...
Objective. Involvement of the gastrointestinal (GI) tract is a rare complication of granulomatosis w...
Malignant atrophic papulosis (MAP) is a rare, obliterating vasculopathy affecting multiple systems, ...
Copyright © 2011 Jakob Burcharth et al. This is an open access article distributed under the Creativ...
Abstract Degos ' disease (malignant atrophic papulosis) is an occlusive arteriopathy involving ...
A case of acute abdomen disease caused by abdominal angiostrongyliasis is reported. A 42-year-old ot...