Dorlands Medical Dictionary Degos disease, syndrome (De·gos disease, syndrome) (dschwagomacrz¢) RobertDegos, French dermatologist, born 1904 malignant atrophic papulosis. http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS
Degos Patients Support Network Website | Forum For Professionals A case of malignant atrophic papulosis successfully treated with nicotine patches. 2Drucker CR. malignant atrophic papulosis response to antiplatelet therapy. http://www.degosdisease.com/forum/forpros/research/dermatology2003exert.htm
Extractions: British Journal of Dermatology 2003 Excerpt SIR , Malignant atrophic papulosis (Degos' disease) is a rare disorder of unknown cause, which is characterized by thrombotic vasculopathy affecting the skin, gastrointestinal tract, central nervous system, and occasionally other organs. It is often lethal because of gastrointestinal involvement. The cutaneous lesions consist of characteristic papules with porcelain-white central atrophy and telangiectatic borders. Similar lesions are seen on the serosal surface of the gastrointestinal tract; perforation of the tract is the most frequent cause of death. Treatments that have been tried for this disorder include antiplatelet therapy (aspirin and dipyridamole), 1,2 fibrinolytic therapy (phenformin and ethyloestrenol), 3 anisoylated plasminogen streptokinase activator and urokinase. 4 However, there is no really satisfactory treatment. 4 We describe a woman with this disorder whose skin lesions and gastrointestinal symptoms were treated successfully with nicotine patches.
Degos Patients Support Network Website | Information | For Professionals malignant atrophic papulosis (MAP), Papulosis Atrophicans Maligna (PAM ), Degosdisease, KohlmeierDegos disease Morbus Kohlmeier-Degos (MKD) an Overview. http://www.degosdisease.com/information/forpros/diagnosing-degos/patientsovervie
Extractions: Chairman of the Department of Dermatology at the University Medical Center Benjamin Franklin , Berlin , Germany . NB This paper is mainly intended to inform patients. Medical terms are used intentionally and then explained in brackets to help patients learn these concepts in order, for example, to understand doctors' reports and scientific literature. The text in italics contains very detailed knowledge and is mainly intended for physicians. Patients may wish to leave out these passages when reading this paper. Introduction Papulosis atrophicans maligna/ malignant atrophic papulosis (MAP) is a rare disease which was first described by Kohlmeier in 1941 (1) and, in the same year, by Degos, who documented it as a separate entity (2). There have been 130 cases described in literature to date. Clinical Presentation It is the characteristic skin changes caused by MAP which are diagnostic indicators.
Malignant Atrophic Papulosis Of Degos rare disorders message board. malignant atrophic papulosis of Degos. Re malignantatrophic papulosis of Degos Miguel González 075302 10/04/00 (0) http://www.healthboards.com/rare-disorders/743.html
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Re: Malignant Atrophic Papulosis Of Degos Re malignant atrophic papulosis of Degos. In Reply to malignant atrophic papulosisof Degos posted by Judith Calder on November 05, 1999 at 113326 http://www.healthboards.com/rare-disorders/1335.html
Extractions: **** Menu **** Home Acne ADD Addiction Addison's Disease Aging Issues AIDS Allergies ALS Alternative Medicine Alzheimer's Anemia Arthritis Asthma Autism Back Problems Bowel Disorders Cancer Caregivers Carpal Tunnel Syndrome Cerebral Palsy Children's Health Chronic Fatigue Common Cold Cosmetic Surgery Cystic Fibrosis Dental Problems Depression Diabetes Digestive Disorders Disabilities Down Syndrome Eating Disorders Epilepsy Fibromyalgia Foot Problems General Health Gulf War Syndrome Headaches Hearing Disorders Heart Disorders Hepatitis Herpes High Blood Pressure High Cholesterol HIV/AIDS Immune Disorders Infectious Diseases Infertility Inner Ear Disorders Irritable Bowel Kidney Disorders Leukemia Lupus Lyme Disease Menopause Men's Health Mental Health Multiple Sclerosis Muscular Dystrophy Myositis Neuromuscular Diseases Neuropathy Osteoporosis Pain Management Parkinson's Polio Pregnancy Rare Disorders Reflex Sympathetic Dystrophy Restless Leg Syndrome Sexual Health Sexually Transmitted Diseaases SIDS Sleep Disorders Smoking Cessation Spinal Cord Disorders Stroke Thyroid Disorders TMJ Disorder Tuberculosis Viagra Weight Loss Women's Health Message Boards on Health Related Topics Click Here to Visit our Sponsor
Extractions: Background This rare disease is important because a skin biopsy may be the first clue to the diagnosis. Patients classically develop multiple skin papules that evolve to have a dimpled appearance with a porcelain white center. This is the clue to the underlying disease which can affect the gastrointestinal tract and central nervous system and may lead to death. The skin biopsy places the pathologist at the center of the diagnostic evaluation. OUTLINE Epidemiology Disease Associations Pathogenesis Laboratory/Radiologic/Other Diagnostic Testing ... Internet Links Köhlmeier-Degos' disease INCIDENCE Rare DISEASE ASSOCIATIONS CHARACTERIZATION Familial cases Rare PATHOGENESIS CHARACTERIZATION Unknown-has been considered a vasculitis, mucinosis, or thrombotic disorder No circulating immune complexes, anti-endothelial cell antibodies, or anticardiolipin antibodies identified ENDOVASCULITIS Some consider a primary endothelial cell defect with secondary thrombosis leading to infarctive changes LUPUS VARIANT
Entrez PubMed Click here to read malignant atrophic papulosis in an infant. We report a7month-old girl with malignant atrophic papulosis (Degos disease). http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra
Entrez PubMed malignant atrophic papulosis (Degos disease) clinical review. Aproposof a case Article in French Sibillat M, Avril MF, Charpentier http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra
Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Degos disease is a rare systemic disorder that affects small and medium sized arteries, causing them to become blocked (occlusive arteriopathy). Degos disease usually progresses through two stages. During the first stage, characteristic skin lesions appear that may last for a period of time ranging from weeks to years. The second stage of Degos disease is most frequently characterized by lesions in the small intestine, but other organs may also be affected. Major symptoms may include abdominal pain, diarrhea, and/or weight loss. Intestinal lesions may break through the wall of the bowel (perforation), a potentially life-threatening complication. The exact cause of Degos disease is unknown. Digestive Disease National Coalition
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Blackwell Synergy - Cookie Absent CASE REPORT. malignant atrophic papulosis in an infant. Summary. We reporta 7month-old girl with malignant atrophic papulosis (Degos disease). http://www.blackwell-synergy.com/links/doi/10.1046/j.1365-2133.2002.04677.x/abs/
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Extractions: Philip M. Parker, INSEAD. Atrophic Definition: Atrophic . Relating to or characterized by atrophy; "atrophic arthritis". Source: WordNet 1.7.1 Specialty definitions using "atrophic" Bordetella bronchiseptica bronchiseptica Pasteurella multocida Poikiloderma Congenitale ... Top Commercial Usage: Atrophic Domain Title Source: compiled by the editor from various references ; see credits. Top Non-Fiction Usage: Atrophic Subject Topic Quote Dentures causing ulceration of the atrophic mucosa over the mandible can initiate ORN. Spontaneous ORN can also occur without any obvious injury to the irradiated mandible. ( references Source: compiled by the editor from ICON Group International, Inc. ; see credits. Top Usage Frequency: Atrophic Atrophic " is generally used as an adjective (general or positive) approximately 100.00% of the time. " Atrophic " is used about 75 times out of a sample of 100 million words spoken or written in English. Its rank is based on over 700,000 words used in the English language. Some parts-of-speech are not covered due to the samples used by the British National Corpus. (note: percents less than one-hundredth of one percent have been omitted)
JW Dermatology -- Sign In Summary and Comment. No Antiphospholipid or Anti Endothelial-CellAntibodies in malignant atrophic papulosis. Malignant atrophic http://dermatology.jwatch.org/cgi/content/full/1995/1201/10
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Degos Disease. Degos disease, also known as malignant atrophic papulosis is a rare disorder. Degosdisease, also known as malignant atrophic papulosis is a rare disorder. http://www.betterhealth.vic.gov.au/bhcv2/bhcarticles.nsf/pages/Degos_disease?ope