Extractions: Lorne Sheldon Label, M.D., M.B.A., F.A.A.N BOOKS/CHAPTERS/PUBLICATIONS BOOKS Lorne S. Label, M.D. Editor in Chief - "Injuries and Disorders of the Head and Brain". Mosby - Year Book Inc. 1997 Chapters PUBLICATIONS Label, Lorne S., Localization of a Subthalamic Locomotor Center, AMSA-UTMB, National Student Research Forum, University of Texas Medical Branch, 1976, p.37. Presented May 1976 Label, Lorne S., Batts, Donald H., Transverse Myelitis Due to Duck Embryo Vaccine, Report of a Case of Review of the Literature. [Archives of Neurology, July 1982, pp. 426-430] Label, Lorne S., Tandan, R., Albers, James, Polyradiculopathy and Hypoglycorrhacia in Malignant Atrophic Papulosis (Kohlmeir-Degos Disease). Neurology V32, No. 3 A152, 1983
Vasculitis Degos Disease is a rare disease, also known as malignant atrophic papulosis, initiallypresenting as a skin condition characterised by red papules with white http://omni.ac.uk/browse/mesh/C0042384L0042384.html
Extractions: low graphics broader: Vascular Diseases other: Angioneurotic Edema Arteriovenous Malformations Cerebrovascular Disorders Hemorrhoids ... Varicose Veins narrower: Behcet's Syndrome Mucocutaneous Lymph Node Syndrome Thromboangiitis Obliterans Vasculitis This interactive tutorial on vasculitis, a group of diseases that causes blood vessels to become inflamed, has been produced by the Patient Education Institute, and made available on the Web by the National Library of Medicine MEDLINEplus service. The tutorial provides background information on vasculitis and covers causes, clinical signs and symptoms, diagnosis, and treatment. Viewing this tutorial requires Flash plug-in. Vasculitis Teaching Materials Patient Education Degos disease This is the Web site of the Degos Patients Support Network. Degos Disease is a rare disease, also known as malignant atrophic papulosis, initially presenting as a skin condition characterised by red papules with white centres, and telangiectasia. Serious (possibly fatal) gastrointestinal and neurologic symptoms usually follow. This Web site brings together what little is know about the condition, providing information for patients and clinicians on symptoms, diagnosis treatment and prognosis. Vasculitis Thromboangiitis Obliterans
Ulcererende Dermatosen waarbij vaak voorkomt (vasculitis, panniculitis, periarteritis nodosa, erythema induratum(Bazin) 2, malignant atrophic papulosis 3, calciphylaxis 4), en http://www.huidziekten.nl/woundcare/ddulcera/dermatosen.htm
Extractions: Ulcererende huidziekten Er bestaan een aantal huidziekten die gepaard gaan met ulceratie als eerste of enige symptoom Daarnaast bestaan er een aantal huidziekten waarbij vaak voorkomt (vasculitis, panniculitis, periarteritis nodosa, erythema induratum (Bazin) [2], malignant atrophic papulosis [3], calciphylaxis [4]), en huidziekten waarbij ulceratie soms kan optreden (sclerodermie, lichen planus, necrobiosis lipoidica, persistant insect bites, lymfoedeem, lipoedeem, erythromelalgia [5], perniosis (chilblains), hemangioma, Stewart Bluefarb syndrome) [6]. Indeling: - pyoderma gangrenosum - parapemphigus e.a. bulleuze dermatosen, - ziekte van Degos (papulosis atrophicans maligna) - erythema exsudativum multiforme - erythema induratum (Bazin), erythema elevatum diutinum - m. Behçet, morbus Paget - heftige contactallergie - ulceratieve lichen planus, sarcoidose, SLE en CDLE, keratosis actinica - insectenbeten - panniculitis, vetnecrose / pancreatic fat necrosis
Index - A To Z Âå¾Ç¹Ï®ÑÀ] - °ê»Ú«p¥Í°·±d¶é°Ï - 24Drs.com and Injuries symptomtopic Male Turner Syndrome nord MaleBC shc Malignant AppendicalTumor nord malignant atrophic papulosis nord Malignant Carcinoid http://www.24drs.com/Health_Guide/health.asp?who=4115.21640
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).
AusMedSites - The Doctors' Reference Site - D Degos disease malignant atrophic papulosis Dementia Care Resources DentalPractice Management Software Dept Health Aged Care Dept of Health http://www.drsref.com.au/ausmedsite.html
Extractions: Research Papers Anstey AV. Photomedicine: Lessons from the Smith-Lemli-Opitz syndrome. J Photochemistry Photobiology 2001; 62: 123-7 Azurdia RM, Anstey AV, Rhodes LE. High cholesterol diet improves the photosensitivity in Smith-Lemli-Opitz syndrome. Br J Dermatol 2001; 144: 143-5 Chave T A, Varma S, Patel G K, Knight A G .Malignant atrophic papulosis (Degos' disease): clinicopathological correlations. JEADV 2001; 15: 43-45. Chowdhury M M U, Chakrabarti A, Prais L, Foulds I S. Occupational allergic contact dermatitis caused by 5,7-dichloro-4(4-fluorophenoxy) quinolone (quinoxyfen). Contact Dermatitis 2001; 45: 119-20. Chowdhury M M U, Motley R J. Treatment of acrodermatitis continua of Hallopeau with oral propylthiouracil and methotrexate. Clin Exp Dermatol 2001; 26: 657-60. Chowdhury M M U, Statham B N. Allergic contact dermatitis from dibutyl phthalate and benzalkonium chloride in Timodine®. Contact Dermatitis 2002; 46: 57.
Extractions: Research Papers ANSTEY AV. Drug reactions and the skin. Medicine 2000; 28: 12: 63-64. CHAVE TA, CHOWDHURY MMU, HOLT PJA. Recalcitrant necrobiotic xanthogranuloma responsive to pulsed oral dexamethasone and maintenance prednisolone. Br J Dermatol 2001; 144: 158-61. CHAVE TA, FINLAY AY, KNIGHT AG - On behalf of the All Wales Dermatology Audit Committee. Thalidomide usage in Wales: the need to follow guidelines. Br J Dermatol 2001; 144: 310-315. CHAVE T, VARMA S, LOGAN R, HOLT PJA. A papillary lesion on the foreskin. Arch Dermatol 2001; 137: 815-20 (off-centre). CHAVE TA, VARMA S, PATEL GK, KNIGHT AG. Malignant atrophic papulosis (Degos' disease): clinicopathological correlations. J Eur Acad Dermatol Venereol 2001; 15: 43-45. CHOWDHURY MMU. The management of psoriasis in primary care. Prescriber 2000; 11(18): 99-107.
Full List Of Skin Conditions BCell 1; Lymphoma - Cutaneous B-Cell 2; Lymphoma - Cutaneous B-Cell3; malignant atrophic papulosis; Malignant Melanoma 1; Malignant http://www.herbaltherapy.net/list_of_skin_conditions.htm
Extractions: "We are living in the NU trition- AGE " Home Full List of Skin Conditions Click on links below to find more information about each condition More Useful Links Dermatology pictures Internet Dermatology Society's Global Lectures Dermatology E-Mail List Services World Wide Dermatology Bulletin Board Helpful Newsgroups: alt.support.skin-diseases alt.support.skin-diseases.psoriasis alt.support.psoriasis Not too pretty.org This site goes into the many products on the market that can be very harmful to you and your children giving us even more reasons to go with all natural ingredients (remember just because a product states "all-natural" doesn't mean it is, always look at the ingredient listing). Click here About Us Testimonies Awards ... Contact Us
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
Contents Of VOLUME 4; NUMBER 2 (OCTOBER) 1997 Sathish Pai B, MD, DVD, CR Srinivas, MD. malignant atrophic papulosis(Degos disease) Report of a rapidly fatal ease. Mostafa http://www.geocities.com/HotSprings/Spa/8355/vol_4_2.html
Extractions: Contents of VOLUME 4; NUMBER 2 (OCTOBER) 1997 Contents Page Histopathology of Cutaneous Leishmaniasis Darius R. Mehregan, MD, David A. Mehregan, MD, Amir H. Mehregan, MD Dyslipidemia Marwan Ramadan, FACRyP, Mohamed Osman Abdel-Rahman, MB FRC Path., Mahmoud A l Zyoud, MD,Amna Mohamed Mohamed Sharif, MRCP, DDS A spectrum of Skin diseases in Dammam Central Hospital (DCH) Eastern Province (EP) Kingdom of Saudi Arabia (K.S.A.). Part one. Dr. Mohammed Mohy El-Din Selim, Dr. Sami Mohammed A 1 Soghair, Dr. Nafeesa Kamel, Dr. Sameeha Arafat House dust allergy in atopic dermatitis patients in Jeddah, Saudi Arabia Obaid Bin-Obaid, MD A cytological study of macrophages in cutaneous leishmaniasis Shahriar Dabiri, MD, Simin Shamsi-Meymandi*, MD, Mohsen Bashiri, MS, Faramarz Soleimani, MSc. Inflammatory linear verrucose epidermal nevus A promising treatment case report Salim Abdul Rahman Al-Harmozi, MBBCh, MSc Mohammed Mohy El-Dine Selim, MD Dermabrasion and cryotherapy in the treatment of verrucous Nevus - a case report Sathish Pai B, MD, DVD, C.R. Srinivas, MD
Connective Tissue Disease Diseases 22 more Diseases All Review Therapy Diagnosis Degos Disease malignant atrophic papulosis U. of Title Abstract http://health-megasite.com/articles/14/connective-tissue-disease.html
Arch Dermatol -- Abstracts: Muller And Landry 112 (3): 357 malignant atrophic papulosis (Degros disease). SA Muller and M. Landry. Twowomen had malignant atrophic papulosis that affected the skin only. http://archderm.ama-assn.org/cgi/content/abstract/112/3/357
Extractions: Vol. 112 No. 3, March 1976 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Muller SA Landry M Contact me when this article is cited S. A. Muller and M. Landry Two women had malignant atrophic papulosis that affected the skin only. Immunologic studies showed normal amounts of serum immunoglobulins and complement and normal delayed hypersensitivity skin test results. Fibrinolysis autografts showed complete loss of fibrinolysis within the lesions but normal fibrinolysis in uninvolved skin. Histopathologic studies showed moderate inflammatory infiltration consisting of lymphocytes in addition to the typical cone-shaped regions of necrobiosis. Large amounts
Arch Dermatol -- Abstracts: Howsden Et Al. 112 (11): 1582 , Contact me when this article is cited. malignant atrophic papulosis ofDegos. Report of a patient who failed to respond to fibrinolytic therapy. http://archderm.ama-assn.org/cgi/content/abstract/112/11/1582
Extractions: Vol. 112 No. 11, November 1976 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Howsden SM Freeman RG Contact me when this article is cited S. M. Howsden, S. J. Hodge, J. H. Herndon and R. G. Freeman
GASNet Anesthesiology: Contents M - R Papulosis. Köhlmeier Degos Disease (malignant atrophic papulosis). ParamyotoniaCongenita. Paramyotonia Congenita (Eulenberg Syndrome). Paralysis. http://www.gasnet.org/pediatric-syndromes/m2r_br.php
Extractions: 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
