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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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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
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
Uncommon Causes Of Stroke - Cambridge University Press KohlmeierDegos disease (malignant atrophic papulosis) Serge Blecic and JulienBogousslavsky; 22. Inflammatory bowel disease Alexander Lossos; 23. http://books.cambridge.org/0521771455.htm
Extractions: Medicine 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. An excellent sorce book for anyone interested in stroke. Neuroradiology, reviewing Stroke Syndromes, first edition
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
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
Extractions: Home Skin conditions 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. 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: 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).
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
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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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
Extractions: 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
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
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
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
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
Extractions: Clinical Resources by Topic: Cardiovascular Disorders Thromboangiitis Obliterans Clinical Resources Emergency Radiology Pathology Genetics ... Miscellaneous Resources See also: Chapter 317: The Vasculitis Syndromes Table of contents Braunwald-Heart Disease: A Textbook of Cardiovascular Medicine 6th Ed.-2001 (MD Consult): Table of contents Medical Library subscription INFO Ruddy: Kelly's Textbook of Rheumatology 6th Ed.-2001 (MD Consult):
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/
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
Extractions: 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).
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
