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81. Segundo Ejemplar De La Revista
disease. Endoscopy, 1991; 23231-233 . kohlmeier-degos´disease with primary intestinal manifestation.
http://www.svcir.org/svc/revistas/5/Artic-2.html
REVISTA VALENCIANA DE CIRUGIA
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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.

82. 1st International Meeting On Degos Disease
dermatology, pathology, neurology, diseases of the gastrointestinal tract, papulosis atrophicans maligna, kohlmeierdegos-Delort-Tricot syndrome,
http://mediconf.de/recstitl/23000104.HTM
MediConf
World Calendar of Medical Events
1st International Meeting on Degos Disease dermatology, pathology, neurology, diseases of the gastrointestinal tract, Degos disease, DD, malignant atrophic papulosis, papulosis atrophicans maligna, Kohlmeier-Degos-Delort-Tricot syndrome, lethal cutaneous and gastrointestinal arteriolar thrombosis For details on this meeting and more meetings in the same field visit our Medical Specialty Calendar MediConf lists over 10000 future events including conferences, workshops, seminars, symposia and exhibitions in the fields of medicine, healthcare, pharmacology, and biotechnology. Every medical specialty is included, from allergy to zoonoses. MediConf is an excellent source of information for healthcare professionals and the pharmaceutical industry worldwide.
Tel: +49-511-443330, Fax: +49-511-442770, E-mail: mediconf@aol.com

83. Wisepress Ltd Stroke Syndromes
Takayasu s Arteritis; 49. Eales disease and GroenbladStrandberg disease; 50.kohlmeier-degos disease; 51. Fabry disease; 52. Behcet s disease; 53.
http://www.wisepress.co.uk/xt_find_product.asp?name=0521453976&mscssid=J7W308BDU

84. The American Journal Of Dermatopathology - UserLogin
Progressive arterial occlusive disease (kohlmeierdegos) a frequently fatalcutaneosystemic disorder. New Engl J Med 1967; 276195-201.
http://www.amjdermatopathology.com/pt/re/ajderm/fulltext.00000372-200104000-0000
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85. Baylor Neurology Case Of The Month
Inflammatory, Behcet’s disease (20 to 25 % of Arabic patients with CVT), Wegener sgranulomatosis, Cogan s syndrome, kohlmeierdegos syndrome,
http://www.bcm.edu/neurol/challeng/pat45/summary.html
Patient #45
Summary and Discussion
S. Tummala, M.D.
Diagnosis: Intracranial Hypertension due to Sigmoid Sinus Thrombosis CASE SUMMARY: The 6 year old boy described in this case, whose clinical symptoms included only headache without papilledema or focal neurological signs, had isolated intracranial hypertension documented by increased opening pressure at lumbar puncture. Substantial clinical improvement in symptoms was observed following the lumbar puncture, as is frequently observed in cases of intracranial hypertension. However, the age and gender of the patient are somewhat atypical in many series of patients with idiopathic intracranial hypertension (pseudotumor cerebri), and the rapid onset of symptoms (over a few days) also raised a concern that the elevated CSF pressure might be secondary to an identifiable cause. MRI and MRV imaging showed evidence of thrombosis of the sigmoid sinus on one side, with normal drainage of the remaining venous system, and no evidence of venous infarction. No evidence of systemic vascular occlusions was evident on the history and general examination. DISCUSSION: The earliest description of cerebral vein and dural sinus thrombosis is attributed to Ribes in 1825. The true incidence of this disorder is unknown, as many cases are asymptomatic or difficult to distinguish from benign symptoms. However, evidence of cerebral vein or sinus thrombosis was documented in 9 percent of 182 consecutive autopsies, with a 2:1 female preponderance. Furthermore, sinovenous thrombosis was diagnosed in 3.75 percent of a pediatric population undergoing angiography. These data suggest that the

86. Kohlmeier Degos Disease
Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes
http://www.amershamhealth.com/medcyclopaedia/medical/Volume IV 1/KOHLMEIER DEGO

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87. Browse By Letter K
Kohler s disease (Volume III 1) Kohler s disease (Volume VII) Kohlmeier degosdisease Kohn, pores of Kommerell diverticulum Konno procedure
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88. What Is Degos? - DegosDisease.com
Kohlmeier Degos disease. Kohlmeier disease. Degos - Kohlmeier disease.Degos disease. Degos syndrome. Erythrokeratoderma en cocardes
http://www.degosdisease.com/information/forpatients/whatisdegos.htm
Degos Disease
What is Degos?
Degos Diesease seems to be a disease of the blood vessels - a thrombotic vasculopathy Cells in the linings of the walls of the medium and small veins and arteries under the skin swell when they become inflamed. This causes the blood flow to be restricted. Where this happens, spots (lesions) appear on the skin. They are small and red, slightly raised.. As they develop, the centre becomes dry and white (atrophic). Sometimes the spots itch. You can see some typical lesions in the picture inset on the left and at the following site:
http://tray.dermatology.uiowa.edu/Degos01.htm
In some people, the disease stays at this stage and other symptoms do not develop. We know of one patient who was diagnosed in 1973 and is still well and working full-time. Be aware that information on some sites is inaccurate . You will read statistics and numbers which might scare you - but they are often based on projections and on published case reports. There are lots of Degos patients whose cases haven’t been written up and who are alive and well. There are also lots of confident assertions which just aren’t true! For example: “This disease affects mainly young men” - not in our experience! Or “The lesions don’t appear on the soles of the feet” - wrong again! Percentages and actual numbers can’t be right, as no-one has compared living patients until now. Take it all with a pinch of salt and add

89. Kohlmeier – Degos Disease
Browse entry words starting with 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, Other characters, Kohlmeier – degos disease,. Print
http://amersham-health.org/medcyclopaedia/volume IV 1/KOHLMEIER DEGOS DISEASE.A

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90. Recurrent Pleural Effusions In Systemic Malignant Atrophic Papulosis (Kohlmeier-
Its rarity and rapidly fatal course make the disease a difficult Intrathoracicmanifestations of Degos’ disease (malignant atrophic papulosis).
http://meeting.chestjournal.org/cgi/content/abstract/126/4/982S
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Pleural Diseases
Tuesday, October 26, 2004 4:15 PM - 5:45 PM
Erica Grabscheid, MD Noah Scheinfeld, MD Mark Rosen, MD, FC and Arvind Bansal, MD Beth Israel Medical Center, New York, NY INTRODUCTION: Malignant atrophic papulosis (MAP), also known distinctive vasculopathy. It is characterized by narrowing and occlusion of the lumen by intimal proliferation and thrombosis, which leads to ischemia and infarction in the involved organ systems. Its rarity and rapidly fatal course make the disease a difficult diagnostic and therapeutic challenge. CASE PRESENTATION: A 38-year-old man was admitted to the hospital with a rash, vomiting and shortness of breath. Five years previously, he developed multiple papular, cutaneous lesions that were distributed mainly on his chest. The skin biopsy revealed morphea. Over

91. Medical Academic Website. +15.500 Journals, Congresses, Powerpoint Presentations
smlaigne syndrome Kocher lorenz fracture Koerner s septum Kohler s disease (VOLUMEIII 1) Kohler s disease (VOLUME VII) Kohlmeier degos disease Kohn, pores of
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Kaposi's sarcoma, genitourinary

92. The World Diseases A 2 Z Names By Countrylinks And Dr Impex
Klinefelter Syndrome. Kohlmeier Degos disease. Krabbe disease. L. Lactose Intolerance.LangerGiedion Syndrome. Laryngitis. Larynx Cancer
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93. Dmoz.fr Health Conditions And Diseases K
disease@ (3)
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94. Goatee.org - The UK Site For Goatees - Anaconda - Shaving
12); Klinefelter Syndrome@ (11); KluverBucy Syndrome@ (3); Kohlmeier-Degosdisease@ (5); Krabbe disease@ (3). Featured Sites K Items
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95. Recurrent Pleural Effusions In Systemic Malignant Atrophic Papulosis (Kohlmeier-

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96. Underwood School PTO - Notices
a 5 year old Newton Corner boy who, this fall lost his battle with KohlmeierDegosdisease, a very rare disorder of the blood vessels.
http://www.underwoodschoolpto.org/Topics/Topic.cfm?TopicName=Notices

97. Health/Conditions And Diseases/Rare Disorders/Degos -- The Doctors Lounge(TM)
Ask the doctor. Get free medical consultation and advice. Choose a medicalspecialist and post your question! Doctors in all medical fields are available.
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