41. Searchalot Directory For M Turner Syndrome (6); malignant atrophic papulosis (4); Malnutrition(8); Mannosidosis (2); Marburg (6); Marfan Syndrome (39); MarieSainton http://www.searchalot.com/Top/Health/ConditionsandDiseases/M/

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42. Conditions And Diseases: M | Treasure Coast Health Disease@ (9); Madelung's Disease@ (11); Malaria@ (36); Male TurnerSyndrome@ (6); malignant atrophic papulosis@ (4); Malnutrition@ (9 http://treasurecoasthealth.com/treasurecoasthealth.php/Health/Conditions_and_Dis

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43. Segundo Ejemplar De La Revista Translate this page Bibliografia. 1.- Degos R. malignant atrophic papulosis. Malignant atrophicpapulosis (Degos' Disease) involving three generations of a family. http://www.svcir.org/svc/revistas/5/Artic-2.html

REVISTA VALENCIANA DE CIRUGIA Crta. ORIHUELA-ALMORADI, s/n 03.314 SAN BARTOLOME Telf. 677 61 66 Ext. 215 Fax. 677 60 60 E-Mail vazquez_jos@gva.es Director J.L. Vázquez Rojas Editor Coeditores Castellon: R. García Calvo Valencia: Milagros Borrego Galán Alicante: Francisco Mauri Barberá Tesorero F. Asencio Arana Consultores J. Aguiló Lucía A. Arroyo A. Baltasar Torrejón R. Calpena Rico J. Cano Ivorra C. Carbonell Antolí F. Delgado Gomis M. Diego Estevez P. Enriquez Valens S. LLedó Matoses E. Marcote Valdivieso B. Narbona Arnau J.V. Roig Vila J. Ruiz del Castillo R. Trullenque Peris Secretaria J. Sánchez Martinez ENFERMEDAD DE DEGOS: UNA CAUSA INFRECUENTE DE PERFORACION INTESTINAL MULTIPLE "ESPONTANEA" (Orihuela). Bibliografia 1.- Degos R. Malignant atrophic papulosis. Br J Dermatol 1997; 100:21-35. 2.- Mckee PH. Vascular diseases. In: Mckee PH, ed. Pathology of the skin with clinical correlations. London: Mosby-Wolfe, 1996: 5.33-5.34 3.- Katz SK, Mudd LJ, Roenigk HH. Malignant atrophic papulosis (Degos' Disease) involving three generations of a family. J Am Acad Dermatol 1997; 37:480-484.

44. THE LIGHTNING HYPERTEXT OF DISEASE. lupus erythematosus = Lupus pernio Vascular disease of the skin = Vascular disorderof skin Degos' disease = malignant atrophic papulosis Livedo reticularis http://www.pathinfo.com/cgi-bin/lh.cgi?tx=papulosis

45. Uncommon Causes Of Stroke - Cambridge University Press Kohlmeier–Degos disease (malignant atrophic papulosis) Serge Blecic and JulienBogousslavsky; 22. Inflammatory bowel disease Alexander Lossos; 23. http://books.cambridge.org/0521771455.htm

Home Catalogue Related Areas: Medicine New titles Email For updates on new titles in: Medicine Uncommon Causes of Stroke Edited by Julien Bogousslavsky, Louis R. Caplan In stock Published as a companion to the second edition of Stroke Syndromes, this comprehensive reference provides in-depth descriptions of many rare and relatively uncommon causes of stroke. Together with Stroke Syndromes, it emphasises pattern recognition in the location and diagnosis of stroke. This is the most comprehensive and authoritative text on stroke of uncommon cause. It describes various forms of angiitis, coagulation disorders, infective, paraneoplastic and metabolic disorders that may be associated with stroke, and a number of individually rare syndromes such as Eales disease, Fabry disease, and pseudoxanthoma elasticum. For all neurologists, neurosurgeons, neuroradiologists and vascular surgeons, it is a unique scientific and clinical resource. It will provide a useful reference to help physicians diagnose and treat stroke patients who do not fit well into the usual clinical categories. Reviews ‘An excellent sorce book for anyone interested in stroke.’Neuroradiology, reviewing Stroke Syndromes, first edition

46. AMEDEO: The Medical Literature Guide TORRELO A, Sevilla J, Mediero IG, Candelas D, Zambrano A. malignant atrophic papulosisin an infant. Br J Dermatol 2002; 146 9168. Abstract Related articles. http://www.amedeo.com/medicine/neo/BRJDERM.HTM

Home Guestbook FAQ Unsubscribe ... AmedeoGroup AMEDEO Internet Services: Free Journals Free Books Amedeo Neonatology Free Subscription Br J Dermatol Abstracts Retrieve all available abstracts of the following 13 articles: HTML format February 2003 Squamous cell carcinoma in a patient with non-bullous congenital ichthyosiform erythroderma. Br J Dermatol 2003; 148: 367-369.. January 2003 KONTOS AP, Ozog D, Bichakjian C, Lim HW. Congenital erythropoietic porphyria associated with myelodysplasia presenting in a 72-year-old man: report of a case and review of the literature. Br J Dermatol 2003; 148: 160-4.. Abstract Related articles December 2002 MARCHINI G, Lonne-Rahm S, Agerberth B, Gudmundsson GH. The newborn infant is protected by an innate antimicrobial barrier: peptide antibiotics are present in the skin and vernix caseosa. Br J Dermatol 2002; 147: 1127-34. Abstract Related articles October 2002 CAMPO-VOEGELI A, Mascaro JM, Casals M, Arimany JL, Amagai M, Camps A. Neonatal pemphigus vulgaris with extensive mucocutaneous lesions from a mother with oral pemphigus vulgaris. Br J Dermatol 2002; 147: 801-805.

47. Degos Disease - Information For Patients And Doctors Degos disease. Degos disease, also known as malignant atrophic papulosisis a rare disorder. It generally occurs in young Caucasian adults. http://www.dermnetnz.org/dna.degos/degos.html

Home Skin conditions Degos disease Degos disease, also known as malignant atrophic papulosis is a rare disorder. It generally occurs in young Caucasian adults. Degos disease affects the lining of the small blood vessels resulting in occlusion (blockage). The blood vessels affected include those supplying the skin, gastrointestinal tract and central nervous system. Degos scar Multiple lesions New lesions What is the cause of Degos disease? The underlying cause of the occlusion of the blood vessels in Degos disease is unknown. Three possible mechanisms are: Viral infection Disturbance in immunity Abnormality in the clotting system of blood What are its features? Skin lesions are the characteristic feature of Degos disease. The lesions are usually multiple and occur predominantly on the trunk and arms. They usually start as small red raised spots of 2-5mm in diameter. After a few days they enlarge and develop a central white spot that is depressed in comparison to the red skin around it. They heal leaving depressed porcelain-white scars. Gastrointestinal complications result from lack of blood supply to the lining of the gut and may lead to serious complications like perforation of the bowel. The usual symptoms are sudden onset of abdominal pain or gastrointestinal bleeding (vomiting blood or passing blood with the bowel motion).

48. GASNet Anesthesiology: Contents D - G Day. Riley Day Syndrome (Familial Dysautonomia). Degos. Köhlmeier - DegosDisease (malignant atrophic papulosis). Denborough. King - Denborough Syndrome. http://gasnet.med.yale.edu/pediatric-syndromes/d2g_br.php

Contents D - G - pediatric syndromes - Dandy Dandy - Walker Syndrome Danlos Ehlers - Danlos Syndrome Day Riley - Day Syndrome (Familial Dysautonomia) Degos Köhlmeier - Degos Disease (Malignant Atrophic Papulosis) Denborough King - Denborough Syndrome Dermal Hypoplasia Corlin - Goltz Syndrome (Focal Dermal Hypoplasia) Diamond Blackfan - Diamond Syndrome DiGeorge DiGeorge Syndrome Disseminated Histiocytosis Letterer - Siwe Disease (Acute Disseminated Histiocytosis) Down Down Syndrome (Trisomy 21) Drager Shy - Drager Syndrome Duchenne Duchenne Muscular Dystrophy Dwarfism Dwarfism (Osteochondrodystrophies) Dysautonomia Riley - Day Syndrome (Familial Dysautonomia) Dystrophic Epidermolysis Cockayne - Touraine Syndrome (Dystrophic Epidermolysis Bullae) Ebstein Ebstein's Anomaly Ectodermal Dysplasia Christ - Siemens - Touraine Syndrome (Anhydrotic Ectodermal Dysplasia) Edward Edward's Syndrome (Trisomy 18) EEC EEC Syndrome Ehlers Ehlers - Danlos Syndrome Eisenmenger Eisenmenger Syndrome Epidermal Necrolysis Lyell Disease (Toxic Epidermal Necrolysis) Epidermolysis Cockayne - Touraine Syndrome (Dystrophic Epidermolysis Bullae) Epidermolysis bullosa Epidermolysis Bullosa Erythema Erythema Multiforme Major (Stevens - Johnson Syndrome) Erythrodermia Ichtyosiform Erythrodermia (Harlequin fetus) Eulenberg Paramyotonia Congenita (Eulenberg Syndrome) Fabry Fabry's Disease (Lysosomal Storage Disease) Familial Familial Periodic Paralysis Fanconi Fanconi's Syndrome (Renal Tubular Acidosis) Farber Farber's Disease Favism Favism Fazio Fazio - Londe Syndrome Feil Klippel - Feil Syndrome Fragile X

49. GASNet Anesthesiology: Contents M - R Papulosis. Köhlmeier Degos Disease (malignant atrophic papulosis). ParamyotoniaCongenita. Paramyotonia Congenita (Eulenberg Syndrome). Paralysis. http://gasnet.med.yale.edu/pediatric-syndromes/m2r_br.php

Contents M - R - pediatric syndromes - Mandibular Dysostosis Treacher - Collins Syndrome (Mandibulofacial Dysostosis) Maple Syrup Maple Syrup Urine Disease (Branched Chain Ketonuria) Marble Bone Disease Albers - Schönberg Disease (Osteopetrosis, Marble Bone Disease) Marfan Marfan's Syndrome Marie Charcot - Marie - Tooth Disease Maroteaux Maroteaux - Lamy Disease McArdle McArdle Disease (Type V Glycogen Storage Disease) McCune McCune - Albright Syndrome Meckel Meckel's Syndrome MEN - Type II Sipple's Syndrome (MEN - type II) Menkes Menkes' Syndrome Merritt Kasabach - Merritt Syndrome Mikity Wilson - Mikity Syndrome Miller Miller's Syndrome Möbius Möbius Syndrome Moon Lawrence - Moon - Biedl Syndrome Morquio Morquio Syndrome (Mucopolysaccharidosis Type IV) Moschkowitz Moschkowitz Disease (Thrombotic Thrombocytopenic Purpura) Moss Gorlin - Chaudhry - Moss Syndrome Mucopolysaccharidosis Type I Hurler Syndrome (Mucopolysaccharidosis Type I) Mucopolysaccharidosis Type II Hunter's Syndrome (Mucopolysaccharidosis Type II) Mucopolysaccharidosis Type III Sanfilippo Syndrome (Mucopolysaccharidosis Type III) Mucopolysaccharidosis Type IV Morquio Syndrome (Mucopolysaccharidosis Type IV) Mucopolysaccharidosis Type V Scheie Disease (Mucopolysaccharidosis Type V) Myasthenia Gravis Myasthenia Gravis Myositis Myositis Ossificans (Fybrodysplasia Ossificans) Myotonia Myotonic Dystrophy (Steinert's Disease) Necrolysis Lyell Disease (Toxic Epidermal Necrolysis) Neonatal Ectopia Cordis Neonatal Ectopia Cordis Neurofibromatosis Neurofibromatosis (von Recklinghausen Syndrome) Nielsen

50. Departmen Of Dermatology - Weekly Activities Erythema Annulare Centrifugum and other Figurate Erythemas Granuloma Annulare -malignant atrophic papulosis (Degos Disease) - Neoplasms, Pseudoneoplasms and http://departments.aub.edu.lb/~webderm/weekly.htm

51. M Cow Disease; @ Madelung's Disease; @ Malaria; @ Male Turner Syndrome;@ malignant atrophic papulosis; @ Malnutrition; @ Mannosidosis; @ Marburg; http://www.ad.com/Health/Conditions_and_Diseases/M/

search Top Categories: MAC @ MPS III @ MRKH @ Machado-Joseph Disease ... @ Myotonic Dystrophy AD.COM Web Directory is based on ODP - Open Directory Project data. No proprietary software was used in the development of this web site. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor

52. Browsing Health Conditions And Diseases M Category Joseph Disease Macular Degeneration Mad Cow Disease Madelung's Disease MalariaMale Turner Syndrome malignant atrophic papulosis Malnutrition Mannosidosis http://www.uksprite.com/search/search/Health/Conditions_and_Diseases/M/

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53. Meckel's 4 A rare cause of perforation of two regions of the gastrointestinal tract isDegos’ disease (malignant atrophic papulosis), a rare form of arteritis. http://www.rcsed.ac.uk/journal/vol46_5/4650014.html

J.R. SAUNDERS, M.P. GRIFFITHS and S.S. KADIRKAMANATHAN Homerton Hospital, Homerton, London, UK Introduction Case report Discussion References J.R.Coll.Surg.Edinb., 46, October 2001, 311-312 Figure 1: Erect chest radiograph demonstrating free intraperitoneal gas INTRODUCTION CASE REPORT DISCUSSION It is a true diverticulum (consisting of all intestinal layers) and is due to the persistence of the vitellointestinal duct. It is present in approximately two percent of the population with a male: female ratio of 2:1 and approximately 20% may contain ectopic gastric mucosa. However, we believe that we are the first to report such a combination of conditions causing perforation in the proximal and distal end of the small bowel. Figure 2: REFERENCES 1. Meckel JF. Arch Physiol Surg Gynecol Obstet Br J Surg 4. Mechat F, Zerouali ON. Non-traumatic perforation of the small intestine. Journal de Chirugie Nippon Geka Gakkai Zasshi j.r.saunders@mds.qmw.ac.uk

54. Plastics6 ectopia lentis, familial RD. Dego's syndrome. malignant atrophic papulosisis rare vasculitis in young M F. multiple red papules 210 http://mail.ml.usoms.poznan.pl/eyemanual/plastics6.htm

Department of Ophthalmology and Visual Sciences The Online Eye Manual / Occuloplastics VI. Systemic Necrobiotic Xanthogranuloma Acanthosis Nigricans Xeroderma Pigmentosa Porphyria ... 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

55. NORD - National Organization For Rare Disorders, Inc. Copyright 1994, 1999, 2000 Synonyms of Degos Disease Degos Syndrome; DegosKohlmeierDisease; Kohlmeier-Degos Disease; malignant atrophic papulosis. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Degos Disease

56. Florida State University College Of Medicine Digital Library contents Buerger Disease (Thromboangiitis Obliterans) Access document;malignant atrophic papulosis Access document. CliniWeb Homepage http://fsumed-dl.slis.ua.edu/clinical/cardiology/cardiovascular/pvd/arterial/thr

Clinical Resources by Topic: Cardiovascular Disorders Thromboangiitis Obliterans Clinical Resources Emergency Radiology Pathology Genetics ... Miscellaneous Resources See also: Cardiovascular Clinical Procedure Resources General Cardiovascular Disorders Clinical Resources Arterial Disorder Prevention and Screening Resources Thromboangiitis Obliterans Patient/Family Resources Harrison's Principles of Internal Medicine 15th Ed.-2001: Table of contents Medical Library subscription INFO Chapter 248: Vascular Diseases of the Extremities Table of contents Arterial Disorders: Access document Thromboangiitis Obliterans: Access document Chapter 317: The Vasculitis Syndromes Table of contents Definition: Access document Classification of Vasculitic Syndromes: Access document Pathophysiology and Pathogenesis: Access document Approach to the Patient: Access document Thromboangiitis Obliterans (Buerger's Disease): Access document Braunwald-Heart Disease: A Textbook of Cardiovascular Medicine 6th Ed.-2001 (MD Consult): Table of contents Medical Library subscription INFO Chapter 41 - Peripheral Arterial Diseases: Access document Vasculitis: Access document Ruddy: Kelly's Textbook of Rheumatology 6th Ed.-2001 (MD Consult):

57. M Website Results :: Linkspider UK Male Turner Syndrome@ (6); malignant atrophic papulosis@ (4); Malnutrition@(8); Mannosidosis@ (2); Marburg@ (6); Marfan Syndrome@ (39 http://www.linkspider.co.uk/Health/ConditionsandDiseases/M/

M Websites from Linkspider UK Keyword: M Linkspider UK Directory M Search for Directory Tree: Top Health Conditions and Diseases : M (0) Add URL Advertise Here! Personalize Amazon ... Myotonic Dystrophy

58. Postgraduate Medicine: Return Of The Painful Leg Ulcers cyanotic macules, painful nodules resembling vasculitic lesions, subungual splinterhemorrhages, blue toe syndrome, malignant atrophic papulosis, and porcelain http://www.postgradmed.com/issues/2002/04_02/puzzles_answer.htm

Return of the painful leg ulcers Ysabel M. Bello, MD; Tania J. Phillips, MD VOL 111 / NO 4 / APRIL 2002 / POSTGRADUATE MEDICINE Return to question The answer Antiphospholipid-antibody syndrome A ntiphospholipid-antibody syndrome (APS) is a multisystem disorder characterized by arterial or venous thrombosis, thrombocytopenia, recurrent fetal loss, and persistently elevated levels of antiphospholipid antibodies (1). Antiphospholipid antibodies are a heterogeneous group of circulating autoantibodies that includes anticardiolipin and anti-beta -glycoprotein I antibodies, which react with phospholipid-protein complexes, and lupus anticoagulants, which interfere with phospholipid-dependent coagulation reactions (2). APS may occur as either a primary disorder or a secondary disorder associated with (1) an underlying systemic disorder, including immunologic disease (most commonly systemic lupus erythematosus [SLE]), cancer, hematologic disease, infection, and neurologic disease, or (2) use of specific drugs (eg, procainamide hydrochloride, chlorpromazine hydrochloride and other phenothiazine derivatives, phenytoin, quinidine, streptomycin sulfate, clozapine) (1,2). Studies of patients with lupus anticoagulants have found that 50% of patients had SLE, while the remainder had various aforementioned disorders (1). Anticardiolipin antibodies are elevated in the presence of a diverse group of infectious agents, including HIV, whereas lupus anticoagulant in patients with HIV infection occurs more commonly with opportunistic infections and tends to disappear when the infection is treated (1).

59. Volume 96, Number 12, December 2001 PérezMateo , and JF Horga. 3462 malignant atrophic papulosis Presentingas Gastroparesis ILP Beales. 3463 Cryptosporidium parvum in http://www-east.elsevier.com/ajg/issues/9612/ajg1201toc.htm

Table of Contents December 2001 Volume , Number Editorials Endoscopic Ultrasound and Pancreatic Cysts: A Sticky Situation! L. V. Hernandez and M. S. Bhutani Cholesterol Crystal Embolization: More Common Than We Thought? J. M. Lawson What Happened to Drug Trials in Ulcerative Colitis? Problems, PPARs, Placebos, and (Possible) Progress A. Kornbluth What's New in GI Delayed Gastric Emptying Should Not Hold Up Antireflux Surgery J. S. Thompson Stapling Away the Pain of Hemorrhoids J. S. Thompson Prefundoplication Esophageal Manometry: Is It Necessary? J. K. DiBaise Clinical Reviews Diagnosis of Celiac Sprue R. J. Farrell and C. P. Kelly A Medical Uncertainty Principle A. Sonnenberg Original Contributions ESOPHAGEAL, GASTROESOPHAGEAL REFLUX DISEASE The Effect of Sildenafil on Lower Esophageal Sphincter and Body Motility in Normal Male Adults P.-L. Rhee J. G. Hyun J. H. Lee Y.-H. Kim H. J. Son J. J. Kim S. W. Paik J. C. Rhee , and K. W. Choi Detection of Incomplete Lower Esophageal Sphincter Relaxation With Conventional Point-Pressure Sensors A. Staiano and R. E.

60. Malignant Atrophic Papulosis (Degos Disease) Selected medical images OMIM malignant atrophic papulosis (Degos disease)Degos disease; Degos' Disease; malignant atrophic papulosis; http://www.gfmer.ch/Genetic_diseases/Malignant_atrophic_papulosis/Malignant_atro

Geneva Foundation for Medical Education and Research Home About Search Medical education ... OMIM Malignant atrophic papulosis (Degos disease) Degos disease Degos' Disease Malignant Atrophic Papulosis Sources DermIS - Dermatology Internet Service (Germany) New Zealand DermNet University of Iowa (US) Print this page Edited by Aldo Campana, March 13, 2003

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