Uncommon Causes Of Stroke - Cambridge University Press KohlmeierDegos disease (malignant atrophic papulosis) Serge Blecic and JulienBogousslavsky; 22. Inflammatory bowel disease Alexander Lossos; 23. http://www.cambridge.org/uk/catalogue/catalogue.asp?isbn=0521771455
Degos . Rare Disorders . Conditions Diseases . Health + forum for patients with Degos disease (malignant atrophic papulosis), theirfamilies and carers and medical advisers. + MD, JD, FAAD. http://www.thema-gute-gesundheit.de/Health|DE-6404-6640|Conditions,and,Diseases|
VASCULITIC SYNDROMES malignant atrophic papulosis (DEGO S DISEASE) is a very rare, lethal cutaneous and Degos R. malignant atrophic papulosis Br J Dermatol 1979;l002l35. http://www.edae.gr/vasculitis-chaidemenos.htm
Extractions: HELLENIC ASSOCIATION DERMATOLOGY-VENEREOLOGY VASCULITIC SYNDROMES: AN APPROACH TO THEIR MANAGEMENT by G.Ch.Chaidemenos, MD State Hospital for Skin and Venereal Diseases, Thessaloniki, Greece. "Vasculitic syndromes" is an all-encompassing term comprising the conditions with vascular inflammation and implying different aetiologic factors but common clinical ana pathologic features. The unaware reader is much embarrassed because several specialties (i.e. dermatologists, dermatopathologists, rheumatologists) use radically different terminology and clinical taxonomy. In order to prevent further confusion, the first disease to deal with in this chapter, is the vasculitis the dermatologist usually encounters in private office or mediCal Center Clinics. NECROTIZING VASCULITIS Also called allergic, hypersensitivity or leukocytoclastic vasculitis or angiitis (from the Greek áããåßïí=lumen) is characterized clinically by palpable purpura often coupled or followed by urticarial, nodular or ulcerative lessons. Fibrinoid necrosis of small vessel walls and leukocytoclasis of the inflammatory cells, in and around the post capillary venular wall, is the histological hallmark of the syndrome. The answer to the question "How should a patient with necrotizing vasculitis be managed?" is not an easy one. Well-experienced authorspropose the following sequence of therapy: Antihistamines, indomethacin plus antihistamines, colchicine, dapsone or hydroxychloroquine, systemic corticosteroids plus azathioprinel1. This approach indicates the relative risk-factors of each treatment modality and what is the best sequence to follow from an idealistic point of view. In every day practice however, dermatologists use much more easily oral corticosteroids, at least for their suppressing effect on the constitutional symptoms.
Fleshandbones Bookshop malignant atrophic papulosis (KohlmeierDegos disease)(ES Roach). Chapter 15.Fibromuscular dysplasia of the cephalic arterial system (BA Sandok). http://www.fleshandbones.com/bookshop/title.cfm?ISBN=0444905030
Extractions: Veterans Home - Quick Links from A to Z - - A - Allergy and Clinical Immunology Ambulatory Surgery Center Anatomical Sciences Anesthesiology Audio Visual Services - B - Biochemistry and Cell Biology Biomedical Engineering Biophysics Biotechnology Breast Care Center Burn Center - C - Cancer Clinical Trials Cancer Prevention Division Cardiology Cell Culture and Hybidoma Facility Center for Cancer Genetics Center for Developmental Genetics Center for Infectious Diseases Centers for Molecular Medicine and Biology Learning Laboratories Center for Structural Biology Children's Dentistry Clinical Lab Sciences Program Comprehensive Epilepsy Center CODY Center for Autism and Developmental Disabilities Cystic Fibrosis Center Cytotechnology Program - D - Dental Medicine Dermatology Dietetic Internship Program - E - Emergency Medicine Endocrinology Fellowship Program Endodontics Epilepsy Center - F - Faculty Senate Family Medicine Flow Cytometry - G - Gastroenterology General Clinical Research Center General Dentistry General Medicine and Geriatrics Gynecologic Oncology Gynecology - H - Health Care Policy and Management Program Health Science Program Heart Center Hematology Hematology and Oncology Fellowship Program Hepatology HIV Treatment - I - Infectious Diseases Internal Medicine and Divisions
Plastics6 malignant atrophic papulosis is rare vasculitis in young M F. multiple red papules210 mm progressing to porcelain white atrophic depressed center http://mail.ml.usoms.poznan.pl/eyemanual/plastics6.htm
Extractions: Amyloidosis Necrobiotic Xanthogranuloma xanthomatous firm lid nodules that ulcerate and progress associated w/conjunctival hyperemia, uveitis, episcleral plaques infiltrative orbital masses w/restrictive motility 80% show paraproteinemia, usually multiple myeloma IgG monoclonal gammopathy, hyperlipidemia, neutropenia Dx: bx w/granulomas in all layers of skin with Touton/FB giant cells Rx : excision, local steroid inj, phasmapheresis, immunosuppressives Acanthosis Nigricans benign pigmented papillomas of epithelium brown velvety hyperkeratotic plaques, symmetric and rarely generalized most commonly in axilla, neck, genitalia, but can be hands, mouth, and eyes no increase in melanin benign: AD, childhood, puberty, without CA pseudo form : w/obesity, endocrine abnl incl insulin resistance, polycystic ovaries malignant form: Xeroderma Pigmentosa rare, AR, defective DNA repair mech, UV damage
GLOBALink - Citations > 24/OCT/2003 A Case of malignant atrophic papulosis Successfully Treated With Nicotine Patches.Kanekura, T., Uchino, Y., Kanzaki, T. British Journal of Dermatology. http://www.globalink.org/33946.shtml
IPS - Uncommon Causes Of Stroke 21. KohlmeierDegos disease (malignant atrophic papulosis) Serge Blecic and JulienBogousslavsky 22. Inflammatory bowel disease Alexander Lossos http://www.ips.com.pl/cgi-bin/opisy.cgi?0521771455&D
Bulletin Of Dermatology And Venerology - Abstracts ¹3 2000 Degos malignant atrophic papulosis. This case report describes clinical andpathohistological features of a Key words papulosis, malignant, atrophic. http://www.mediasphera.aha.ru/dermatol/2000/3/e3-00ref.htm
Extractions: Clinico-immunological evaluation of therapeutic efficiency of leukinferon in patients with Kaposis sarcoma The objective of this study was to evaluate effects of leukinferon on the general clinical condition and immune status of 40 patients with Kaposis sarcoma. It has been demonstrated that treatment with leukinferon results in a reduced frequency of side effects caused by prospidine therapy. Leukinferon produces good therapeutic effect in patients receiving low doses of prospidine and may be recommended for monotherapy of Kaposis sarcoma in elderly subjects to whom the latter product is contraindicated. Results of the study show that the inclusion of leukinferon in the combined therapy of Kaposis sarcoma leads to a considerable improvement of the initially abnormal levels of immunocompetent and phagocytizing cells.
KoreaMed - Basic Search A case of malignant atrophic papulosis (Degos disease). J Korean Pediatr Soc.1991 Dec;34(12)17241729. Korean. 6, Pai KS, Chung YM, Namgung R, Lee C, http://www.koreamed.org/SearchBasic.php?QY=J Korean Pediatr Soc [JTI] AND 1991 [
Papulosis, Malignant Atrophic Base de données sur les maladies rares et les médicaments orphelins. http://www.orpha.net/static/GB/papulosis.html
WebMD With AOL Health - Degos Disease Degos Syndrome; DegosKohlmeier Disease; Kohlmeier-Degos Disease; malignant AtrophicPapulosis. Disorder Subdivisions. None. General Discussion http://aolsvc.health.webmd.aol.com/hw/heart_disease/nord991.asp
Extractions: You are in Condition Centers Choose a Topic All Conditions ADD/ADHD Allergies Alzheimer's Arthritis Asthma Back Pain Bipolar Disorder Cancer Cholesterol Management Dental Health Depression Epilepsy Eye Health Heart Disease Heartburn/GERD Hypertension Infertility Men's Conditions Migraines/Headaches Multiple Sclerosis Pain Management Sexual Health Stroke Weight Management Women's Conditions 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.
NORD - National Organization For Rare Disorders, Inc. Degos Syndrome; DegosKohlmeier Disease; Kohlmeier-Degos Disease; malignant AtrophicPapulosis. Disorder Subdivisions. General Discussion http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Degos Disease
Medicine 2001 Publications - Cardiff University Chave, T., Varma, S., Patel, G., and Knight, A., 2001, malignant atrophicpapulosis (Degos disease) clinicopathological correlations, JEADV 154345. http://www.cardiff.ac.uk/research/publications/pubs/year2001/medipubs2001.html
Extractions: Search: Contact Us A-Z Index Cymraeg Home ... Mathematics Medicine* Music Nursing and Midwifery* Optometry and Vision Sciences Pharmacy ... Welsh Research Ali, M. S., Harmer, M., Vaughan, R. S., Dunne, J., and Latto, I. P., 2001, Cerebral oxygenation measured by spatially resolved spectroscopy (NIRO-300) does not agree with jugular bulb oxygen saturation in patients undergoing warm coronary artery bypass surgery., Canadian Journal of Anaesthesia Dingley, J., King, R., Hughes, L., Terblanche, C., Mahon, S., Hepp, M., Youhana, A., and Watkins, A., 2001, Exploration of xenon as a potential cardiostable sedative: a comparison with propofol after cardiac surgery, Anaesthesia Foy, J ., 2001, Gabapentin in post herpetic neuralgia: a randomised double blind placebo controlled study., Pain Vaughan, R ., 2001, Pain relief after thoracotomy., British Journal of Anaesthesia Zatman, T. F., Hall, J. E., and Harmer, M ., 2001, Gastric residual volume in children: a study comparing efficiency of erythromycin and metoclopramide as prokinetic agents, Br J Anaesth Anderson, R. A., Jones, C. J., and Goodfellow, J
