41. Degos Disease (Malignant Atrophic Papulosis), Eastern Carolina Degos Disease (malignant atrophic papulosis) University Health Systems ofEastern Carolina serves tarboro, ahoskie, edento, winsor, maxhead, dear county, http://www.uhseast.com/175550.cfm

Health News Health Library Health Topics Healthy Living ... Nutrition Self-Help Resources Information about national and local self-help organizations and support groups. Degos Disease (Malignant Atrophic Papulosis) 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. Degos Patients Support Network Online. Mutual support, encouragement and information for persons with Degos disease (aka malignant atrophic papulosis) a rare disease. Forums for patients and medical professionals. E-MAIL: judithcalder@degosdisease.com WEBSITE: dedosdisease.com VERIFIED: 9/14/2004 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

42. Malignant Atrophic Papulosis. Report Of A Case With Multiple Ophthalmic Findings Indian J Ophthalmol, Official scientific journal of the All India OphthalmologicalSociety (AIOS) http://www.ijo.in/article.asp?issn=0301-4738;year=2003;volume=51;issue=3;spage=2

43. Blackwell Synergy - Cookie Absent Progressive systemic sclerosis with malignant atrophic papulosis. Lesionsresembling malignant atrophic papulosis in a patient with dermatomyositis. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1468-3083.2004.01181.x

Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

44. Blackwell Synergy - Cookie Absent Painful penile ulceration in a patient with malignant atrophic papulosis Six cases of malignant atrophic papulosis (Degos disease) occurring in one http://www.blackwell-synergy.com/doi/abs/10.1111/j.1468-3083.2005.01227.x

Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

45. Degos Disease We report a 7month-old girl with malignant atrophic papulosis (Degos disease) . Degos disease, or malignant atrophic papulosis, is a rare obstructive http://www.thedoctorsdoctor.com/diseases/degos_disease.htm

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 EPIDEMIOLOGY CHARACTERISTICS SYNONYMS Malignant Atrophic Papulosis Köhlmeier-Degos' disease INCIDENCE Rare AGE Usually 4-6th decades Malignant atrophic papulosis in an infant. Torrelo A, Sevilla J, Mediero IG, Candelas D, Zambrano A. Department of Dermatology, Hospital del Nino Jesus, Menendez Pelayo 65, 28009 Madrid, Spain. Br J Dermatol. 2002 May;146(5):916-8. Abstract quote We report a 7-month-old girl with malignant atrophic papulosis (Degos' disease). She also showed spontaneous aggregation of platelets. A good clinical response was obtained by treatment with aspirin and dipyridamole.

46. Cancer And Scleroderma By The International Scleroderma Network (ISN) malignant atrophic papulosis (MAP) or Degos Syndrome. Lesions resembling malignantatrophic papulosis in a patient with progressive systemic sclerosis http://www.sclero.org/medical/symptoms/associated/cancer/a-to-z.html

www.sclero.org So you'd like to learn more about scleroderma? an Amazon guide by Shelley Ensz, ISN President Our site menu requires pop-ups and javascript enabled. About the ISN Join/Donate Languages Medical Scleroderma Experts Symptoms Newsroom Message Board Support Stories Support Groups SWA Sites to Surf! Hope on Horizon ISN Gift Shop Email ISN ISN Medical

47. Scleroderma Medical News April 2005 Lesions resembling malignant atrophic papulosis in a patient with progressivesystemic sclerosis. malignant atrophic papulosis (MAP), or Degos syndrome, http://www.sclero.org/news/medical/2005/04-apr.html

www.sclero.org So you'd like to learn more about scleroderma? an Amazon guide by Shelley Ensz, ISN President Our site menu requires pop-ups and javascript enabled. About the ISN Join/Donate Languages Medical Scleroderma Experts Symptoms Newsroom Message Board Support Stories Support Groups SWA Sites to Surf!

48. Eastern Mediterranean Health Journal, Vol. 6 No. 1, Degos Disease In A 24-year-o Degos disease (malignant atrophic papulosis) is a rare disease that affects skinand the gastrointestinal, ocular and central nervous systems. http://www.emro.who.int/Publications/EMHJ/0601/25.htm

Eastern Mediterranean Health Journal Back to Health Journal page Health Journal back issues Home Degos disease in a 24-year-old Jordanian male R.M. Al-Smadi, F. Abu-Jamous and I. Omeish Volume 6, Issue 1, 2000, Page 194-196 Introduction Degos disease (malignant atrophic papulosis) is a rare disease that affects skin and the gastrointestinal, ocular and central nervous systems. The disease is characterized by papules that develop porcelain-white centres and telangiectatic borders. The etiology of the disease is unknown; however, the immediate cause may lie in impaired endothelial function or abnormal coagulation (fibrinolytic activity). Viral causes have been implicated. Histopathological findings are wedge-shaped areas of dermal necrosis covered by markedly atrophic malpighian layers and collagen with a smudged appearance. Complications of the disease include peritonitis, intestinal perforation and, less frequently, cerebral infarction. There is no effective treatment; however, antiplatelet therapy may be beneficial for patients in whom platelet aggregation is impaired. Prognosis is poor when systemic involvement is found, but seems to be good in benign forms.

49. ILDS - ICD10 malignant atrophic papulosis of Degos. I77.800, Papulosis, malignant atrophic.I78.010, Angiomatosis Osler Weber Rendu. I78.010 http://web.ilds.org/icd10_list.php?VIEW=1&START_CODE=I74.4&START_EXT=10

50. Karger Publishers 15 Kanekura T, Uchino U, Kanzaki T A case of malignant atrophic papulosissuccessfully treated with nicotine patches. Br J Dermatol 2003;149660662. http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=

51. Köhlmeier-Degos Syndrome (www.whonamedit.com) malignant atrophic papulosis, malignant papulosis atrophicans, malignantpapulosis with atrophy; papulosis atrophicans maligna, http://www.whonamedit.com/synd.cfm/3466.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Köhlmeier-Degos syndrome Also known as: Degos’ disease Degos-Delort-Tricot syndrome Köhlmeier's syndrome Thrombangitis cutaneo-intestinalis disseminata Köhlmeier-Degos Synonyms: Arteriolar cutaneo-gastrointestinal thrombosis, atrophic dermatitis papulosquamosa¸ atrophic pulosquamous dermatitis, clear cell acanthema syndrome, cutaneointestinal mortal syndrome, cutaneomuco-intestinal syndrome; dermatitis papulosquamosa atrophicans, disseminated endangitis, fatal cutaneointestinal syndrome, malignant atrophic papulosis, malignant papulosis atrophicans, malignant papulosis with atrophy; papulosis atrophicans maligna, thromboangiitis cutaneo-intestinalis disseminata, ulérythème porcelainé en gouttes (French). Associated persons: Robert Degos Joseph Delort W. Köhlmeier

52. Intrathoracic Manifestations Of Degos' Disease (malignant Atrophic Papulosis) -- Degos disease (malignant atrophic papulosis) is a rare multisystemic diseasewith characteristic cutaneous lesions, abdominal symptoms and often rapidly http://www.chestjournal.org/cgi/content/abstract/73/1/79

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Order Full text via Infotrieve Submit a response Alert me when this article is cited Alert me when eLetters are posted ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Pierce, R. N. Articles by Smith, G. J. ARTICLES Intrathoracic manifestations of Degos' disease (malignant atrophic papulosis) RN Pierce and GJ Smith Degos' disease (malignant atrophic papulosis) is a rare multisystemic disease with characteristic cutaneous lesions, abdominal symptoms and often rapidly fatal course. Our review of the reported intrathoracic involvement in the more than 60 reported cases of Degos' disease suggests that pleuritis and pericarditis are manifestations of the underlying pathophysiologic process. Seventeen of these reported cases were said to

53. CNS Involvement In Malignant Atrophic Papulosis (Kohlmeier-Degos Disease): Vascu CNS involvement in malignant atrophic papulosis (KohlmeierDegos disease)vasculopathy and coagulopathy. DK Dastur, BS Singhal and HJ Shroff http://jnnp.bmjjournals.com/cgi/content/abstract/44/2/156

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Dastur, D. K. Articles by Shroff, H. J. Journal of Neurology, Neurosurgery, and Psychiatry, 1981, Vol 44, 156-160 PAPERS CNS involvement in malignant atrophic papulosis (Kohlmeier-Degos disease): vasculopathy and coagulopathy DK Dastur, BS Singhal and HJ Shroff The clinical features in a 42 year old man with malignant atrophic papulosis with CNS involvement are described. They included mental dysfunction, paraesthesiae, weakness of left limbs, with pyramidal tract

54. JW Dermatology -- Sign In malignant atrophic papulosis (Degos disease) is a rare, Malignant atrophicpapulosis appears both clinically and histologically to be a disorder of http://dermatology.jwatch.org/cgi/content/full/1995/1201/10

Physician-authored summaries and The New England Journal of Medicine Please sign in for full text All customers have full-text access to the Journal Watch publication(s) to which they have a subscription. Other registered users have access to Journal Watch Online content older than six months and may request e-mail notification of current contents. Subscribers and Registered Users User Name Password If you are a subscriber using Journal Watch Online for the first time you must activate and choose a password Remember my user name and password. Forgotten your password? If you do not use cookies sign in here (After you click the 'Sign In' button you may have to wait for several seconds. Thank you for your patience.) First-Time Users and Other Visitors To subscribe click here. If you would like free e-mail notification of current content and/or free access to all content older than 6 months register here If you would like full access to Journal Watch Online for 7 days for $19

55. ?050427 Translate this page malignant atrophic papulosis in an infant. Br J Dermatol, 2002, 146 916-918 . malignant atrophic papulosisresponse to antiplatelet therapy. http://www.wanfangdata.com.cn/qikan/periodical.Articles/zhpf/zhpf2005/0504/05042

56. Myelomalacia And Hypoglycorrhachia In Malignant Atrophic Papulosis -- Label Et A Myelomalacia and hypoglycorrhachia in malignant atrophic papulosis A 25year-oldman with the skin lesions of malignant atrophic papulosis had clinical http://www.neurology.org/cgi/content/abstract/33/7/936

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Correspondence: Submit a response Alert me when this article is cited Alert me when Correspondence are posted ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Label, L. S. Articles by Albers, J. W. ARTICLES Myelomalacia and hypoglycorrhachia in malignant atrophic papulosis LS Label, R Tandan and JW Albers A 25-year-old man with the skin lesions of malignant atrophic papulosis had clinical and electrodiagnostic evidence of a multifocal asymmetric myelomalacia or polyradiculopathy in association with elevated CSF protein and hypoglycorrhachia. Autopsy findings included widespread infarctions and necrosis of brain, brainstem, and spinal cord. The combined clinical and laboratory findings were similar to those seen in systemic lupus erythematosus, sarcoidosis, or meningeal carcinomatosis. Thus, malignant

57. Malignant Atrophic Papulosis (Kohlmeier-Degos Disease) In Childhood -- Horner Et malignant atrophic papulosis (KohlmeierDegos disease) is reported for the firsttime with pathologic verification of central nervous system involvement in http://www.neurology.org/cgi/content/abstract/26/4/317

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Correspondence: Submit a response Alert me when this article is cited Alert me when Correspondence are posted ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by Horner, F. A. Articles by Choi, B. H. ARTICLES Malignant atrophic papulosis (Kohlmeier-Degos disease) in childhood FA Horner, GJ Myers, DA Stumpf, BJ Oseroff and BH Choi Malignant atrophic papulosis (Kohlmeier-Degos disease) is reported for the first time with pathologic verification of central nervous system involvement in a child. The disease began in infancy with rare recurring skin lesions; the child died at the age of 7, after progressive neurologic deterioration. Diagnosis was suspected clinically and confirmed by biopsy of a typical skin lesion. Recognition of this disorder by its dermatologic

58. MAL – MEA malignant atrophic papulosis http//directory.ansme.com/health/168.html.malignant atrophic papulosis http//my.webmd.com/content/healthwise/30/7398 http://www.healthmednet.com/MAL-MEA.htm

59. Dermatomyositis - November 1, 2001 - American Family Physician Hypertrichosis Malignant erythema Urticaria/urticarial vasculitis Partiallipodystrophy malignant atrophic papulosis (Degos disease) Zebralike striping http://www.aafp.org/afp/20011101/1565.html

Advanced Search AAFP Home Page Journals Vol. 64/No. 9 (November 1, 2001) Dermatomyositis RIC ANTHONY KOLER, MAJ, MC, USA, Fox Army Health Center, Redstone Arsenal, Alabama ANDREW MONTEMARANO, MAJ, MC, USA, Walter Reed Army Medical Center, Washington, D.C. Dermatomyositis is an idiopathic inflammatory myopathy with characteristic skin manifestations. Although the disorder is rare, with a prevalence of one to 10 cases per million in adults and one to 3.2 cases per million in children, early recognition and treatment are important ways to decrease the morbidity of systemic complications. An association with other connective tissue disorders (overlap syndrome) and malignancy make this diagnosis particularly important to primary care physicians. Patient management includes careful evaluation for underlying malignancy and liberal use of physical therapy, antihistamines, sunscreen and oral corticosteroids. Poor prognostic indicators include poorly responsive disease, delay in diagnosis and the presence of malignancy. The therapeutic goal is to maintain function and prevent or minimize sequelae. (Am Fam Physician 2001;64:1565-72.) A patient information handout on dermatomyositis and polymyositis, written by the authors of this article, is provided on the

60. AJNR -- Sign In Page Summary Degos disease, or malignant atrophic papulosis, Degos disease (alsoknown as malignant atrophic papulosis or KohlmeierDegos disease) is a rare http://www.ajnr.org/cgi/content/full/26/3/646

HOME HELP FEEDBACK SUBSCRIPTIONS ... SEARCH QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This item requires a subscription to American Journal of Neuroradiology Online. Full Text Nervous System Involvement in Degos Disease Amato et al. AJNR Am J Neuroradiol. This Article Abstract Figures Only Full Text (PDF) ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Amato, C. Articles by Moschini, M. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password? Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 7 days for US$10.00 Pay for Admission - You may access all content in American Journal of Neuroradiology Online (from the computer you are currently using) for 7 days for US$25.00.

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 3     41-60 of 98    Back | 1  | 2  | 3  | 4  | 5  | Next 20