Extractions: This Article Full Text (PDF) Services Similar articles in this journal Alert me to new issues of the journal Download to citation manager PubMed Articles by Bansal, A. Tuesday, October 26, 2004 4:15 PM - 5:45 PM Erica Grabscheid, MD Noah Scheinfeld, MD Mark Rosen, MD, FC and Arvind Bansal, MD Beth Israel Medical Center, New York, NY INTRODUCTION: Malignant atrophic papulosis (MAP), also known distinctive vasculopathy. It is characterized by narrowing and occlusion of the lumen by intimal proliferation and thrombosis, which leads to ischemia and infarction in the involved organ systems. Its rarity and rapidly fatal course make the disease a difficult diagnostic and therapeutic challenge. CASE PRESENTATION: A 38-year-old man was admitted to the hospital with a rash, vomiting and shortness of breath. Five years previously, he developed multiple papular, cutaneous lesions that were distributed mainly on his chest. The skin biopsy revealed morphea. Over
Extractions: Vol. 114 No. 11, November 1978 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Stahl D Hou-Jensen K Contact me when this article is cited D. Stahl, K. Thomsen and K. Hou-Jensen On electron microscopy of the endothelial cells of a patient with cutaneous and CNS symptoms of malignant atrophic papulosis, paramyxovirus-like particles could be seen in the cytoplasm. These particles were interpreted as degenerative changes that were due to ischemia. Coagulation studies showed increased thrombocyte aggregation, and treatment with the platelet-suppressive drugs, aspirin and dipyridamole, was instituted. This
Extractions: Vol. 112 No. 11, November 1976 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Howsden SM Freeman RG Contact me when this article is cited S. M. Howsden, S. J. Hodge, J. H. Herndon and R. G. Freeman
Degos Patients Support Network Website Forum For Professionals A case of malignant atrophic papulosis successfully treated with nicotine patches.SIR , malignant atrophic papulosis (Degos disease) is a rare disorder of http://www.degosdisease.com/foruminfo/forpros/research/dermatology2003exert.htm
Extractions: @import url(default.css); Online Health Information Back to Health Library Print This Page Email to a Friend Degos Patients Support Network This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site. Online. The above information was "verified" as correct on the date at the end of each entry. Since American Self-Help Group Clearinghouse's database is extensive but staffing is limited and information for these organizations can change, it is not possible to keep every entry in American Self-Help Group Clearinghouse database completely current and accurate. Please check with the organizations listed for the most current information. For additional information on self-help groups, please visit the American Self-Help Group Clearinghouse web site at http://www.mentalhelp.net/selfhelp
DermIS / Main Menu / DOIA / Malignant Atrophic Papulosis / Info information on the diagnosis malignant atrophic papulosis If you are apatient with malignant atrophic papulosis , please complete our http://dermis.multimedica.de/doia/diagnose.asp?zugr=d&lang=e&diagnr=447800&topic
WebMD With AOL Health - Index Degos Disease (malignant atrophic papulosis) Shc Degos Patients SupportNetwork Degos Disease (malignant atrophic papulosis) Shc http://aolsvc.health.webmd.aol.com/hw/index/index-all-D.asp
Entrez PubMed malignant atrophic papulosis (MAP), or Degos syndrome, is a rare disorder ofunknown etiology. It is characterized by a deep subcutaneous vasculopathy http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
Entrez PubMed We report a 7month-old girl with malignant atrophic papulosis (Degos disease).She also showed spontaneous aggregation of platelets. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=2
Dorlands Medical Dictionary malignant atrophic papulosis, an often fatal disease occurring most often in men,characterized by endovasculitis of the skin, gastrointestinal tract, http://www.merckmedicus.com/pp/us/hcp/thcp_dorlands_content.jsp?pg=/ppdocs/us/co
The American Journal Of Dermatopathology - UserLogin malignant atrophic papulosis, first described by Kölmeier in 1941 as a cutaneous Characteristic histopathologic findings of malignant atrophic papulosis http://www.amjdermatopathology.com/pt/re/ajderm/fulltext.00000372-199908000-0001
The American Journal Of Dermatopathology - UserLogin malignant atrophic papulosis (Degos disease) involving three Feuerman EJ,Dollberg L, Salvador O. malignant atrophic papulosis with mucin in the http://www.amjdermatopathology.com/pt/re/ajderm/fulltext.00000372-200104000-0000
Health Library - Degos Disease (malignant atrophic papulosis) and information for persons withDegos disease (aka malignant atrophic papulosis) a rare disease. http://yalenewhavenhealth.org/library/healthguide/en-us/SelfHelp/topic.asp?hwid=
Print Manager Degos Disease (malignant atrophic papulosis). Table of Contents. Degos Disease (MalignantAtrophic Papulosis). This information is provided as a resource http://yalenewhavenhealth.org/WebApps/PrintFriendly/PrintManager.aspx?URL=/libra
