Pathology Of The Skin: With Clinical Correlations, 2nd Ed Reticulate pigmented anomaly of the flexures(Dowlingdegos disease) 2.32.Pseudoxanthoma elasticum (Grijnblad-Strandberg syndrome) 2.33. http://www.hanilmed.com/division/titleimg/patholoy/63.html
Extractions: This dualistic approach which formed the basis for the first edition has been expanded in the second edition, which includes over 3000 colour pictures that extensively illustrate each entity. The text is substantially enlarged, aiming to provide a completely comprehensive text including over 100 new entities, more dermatological rarities with relevant histology, and increased AIDS-related skin pathology. In addition to conventional histopathology and immunofluorescence, greater space has been devoted to Immunohistochemistry and, when appropriate, to the application of molecular biological techniques. The reference lists have not only been updated, they have been greatly expanded and all references are now cited in the text. It is hoped that this new approach will provide an invaluable resource for literature in dermatopathology. The second edition has taken more than three years to write. If, as hoped, it is of help to pathologists when faced with difficult or unusual conditions, then the time will have been well spent.
JAMA -- Page Not Found Incredibly thorough, the book also covers more extraordinary causes of stroke,such as Kohlmeierdegos disease, pseudoxanthoma elasticum, progeria, and http://jama.ama-assn.org/issues/v287n12/ffull/jbk0327-4.html
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Browsing Health Conditions And Diseases D Category Dandy Walker Syndrome De Lange Syndrome Deafblindness Deafness degos diseaseDementia Dengue Fever Depersonalization Disorder Depression Dercum Disease http://www.uksprite.com/search/search/Health/Conditions_and_Diseases/D/
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Open Directory - Health: Conditions And Diseases: D 9); Deafness@ (116); degos disease@ (4); Dementia@ (60); Dengue Fever@(10); Depersonalization Disorder@ (9); Depression@ (269); Dercum http://www.mptdo.com/Health/Conditions_and_Diseases/D/
Developmental And Genetic Diseases Lumbosacral agenesis; Maceration; Mal de Meleda; Malignant atrophicpapulosis (degos disease); MardenWalker syndrome; Marfan syndrome; http://www.gfmer.ch/Selected_images/Developmental_genetic_diseases.htm
A Listing Of Disorders Darier Disease. De Barsy Syndrome. De Santis Cacchione Syndrome. degos disease.Dejerine Sottas Disease. Depression. Dercum Disease. Dermatomyositis. Devic Disease. http://medschool.umaryland.edu/BTBank/Family/Disorders_D.htm
Extractions: University of Maryland, Baltimore D Dandy Walker Malformation Darier Disease De Barsy Syndrome De Santis Cacchione Syndrome Degos Disease Dejerine Sottas Disease Depression Dercum Disease Dermatomyositis Devic Disease Dextrocardia with Situs Inversus Diabetes, Insulin Dependent Diaphragmatic Hernia Diastrophic Dysplasia Diencephalic Syndrome DiGeorge Syndrome Dilatation of the Pulmonary Artery, Idiopathic DOOR Syndrome Down Syndrome Dracunculosis Drash Syndrome Duane Syndrome Dubin Johnson Syndrome Dubowitz Syndrome Duhring Disease Duodenal Atresia or Stenosis Dyggve Melchior Clausen Syndrome Dysautonomia, Familial Dyschondrosteosis Dyskeratosis Congenita Dyslexia Dysphonia, Chronic Spasmodic Dysplasia, Epiphysealis Hemimelica Dysplasia, Fibrous Dysplastic Nevus Syndrome Dystonia Dystonia, Blepharospasm Dystonia, Torsion Dystrophy, Asphyxiating Thoracic Dystrophy, Myotonic
Clinical Case cells (Fig.1), the pericytes and the macrophages descibedfot he erythematous lupusas it also shows the cylinders mentioned in the Case 2 (degos disease). http://www.dermocosmos.com/ingles/Clinical_Cases/solen3.htm
Extractions: rd CLINICAL CASE This is a progressive dermatomyositis in a child, with its clinical features; muscular pain when walking or when being palpated, difficulties in climbing stairs, in combing the hair, in eating, etc. with typical and also progressive cutaneous signs of periorbital erythemas that slightly appear in some other spots, turn to purple with reticular livedo and zones with white atrophia. The laboratory findings confirm the muscular affection and the histopathology is quiet recognizable for its leucocytic vasculitis. It is also very aggressive considering the emarkable epifdermic lesion we can observe and that let us think, at the very beginning, to a viral infection. Electronic microscopy puts into relief, once again, the intracytoplasmic tubuloreticular structures of the enothelial cells (Fig.1), the pericytes and the macrophages descibedfot he erythematous lupus as it also shows the cylinders mentioned in the Case 2 (Degos Disease). The first time those cylinders were detected was in a dermatomyositis (Fig.2). They were then found again in the Degos Disease, in the T cells leucemia and in AIDS. There is certainly an etiopathologic explanation for this phenomenon as far as the structures are themselves a degeneration of the endopasmic reticle with a strong predominance in some diseases, in certain cells, at some stage of evolution. These ultrastructural markers should not be neglected during viral investigations. Fig.1
Dowling-Degos´ Disease Beim Verarbeiten des URL ist ein Fehler aufgetreten. Bitte klicken Sie hier um zur Startseite zurückzukehren. http://www.dermis.net/bilddb/diagnose/englisch/i009605.htm
PaperChase Search Page (custom) An atypical paediatric case of malignant atrophic papulosis (Kohlmeierdegosdisease). degos'disease who died as a result of intestinal involvement. http://www.paperchase.com/docs/R1603/F205201/B16.htm
Extractions: A new case of malignant atrophic papulosis (Kohlmeier-Degos disease) is reported. Vascular symptoms began at 17 months of age with cerebral ischaemia and progressive involvement of fingers and toes with torpid ulcers and apical necrotic amputations. At 6 years of age he developed chronic intestinal ischaemia with malabsorption and a new cerebral attack; in spite of Top of Abstract anti-aggregant therapy the disease progressed and he died 7 months after diagnosis from a third cerebral ictus. Since the typical skin lesions of the disease were absent, the diagnosis was made on the basis of a pathological pattern of an occluded biopsied artery. The elder brother presents clinical and instrumental vascular involvement without cutaneous lesions and could be slightly affected.
Extractions: Quelques aspects de la contribution de Robert Degos à la Dermatologie Jean CIVATTE Robert Degos est et restera une des grandes figures de la dermatologie non seulement française mais mondiale: en ce dixième anniversaire de sa mort il n'est que juste de s'en souvenir. Une façon d'évoquer sa mémoire consiste à rappeler, sinon toutes, du moins les princiales affections qu'il a décrites ou dont il a précisé les cadres nosologiques. Certaines maladies portent à juste titre son nom. La principale est la papulose atrophiante maligne. Elle est née le 12 février 1942. Cette évolution fatale est rapportée par les mêmes auteurs le 21 mai 1942 sous le titre "dermatite papulo-squameuse atrophiante (Epilogue)": cette appellation est donc, pour l'instant, conservée pour cette affection qui comporte les mêmes altérations histologiques sur la peau et l'intestin et qui fait discuter, mais pour l'éliminer, un lupus érythémateux aigu, en particulier du fait de l'absence de fièvre. En 1948, R.Degos,J.Delort et R.Tricot présentent devant la Société Médicale des Hôpitaux de Paris un travail sur ce même sujet avec, comme titre, "papulose atrophiante maligne (syndrome cutanéo-intestinal mortel)". Ils utilisent à nouveau ce nom, qui est désormains unaninement accepté, dans un article publié en 1952 dans les Annales de Dermatologie dans lequel ils rappellent leur observation, celle de Tzanck, Civatte et Sidi, et citent un cas présente en juin 1950 par F.P.Merklen et F.Cottenot qu'ils rapprochent du leur, mais sans l'y assimiler faute de renseignements suffisants. Depuis, le nom de maladie de Degos, ou Degos's disease ou syndrome dans la littérature anglo-saxonne, est adopté partout.
Robert Degos (1904-1987) several dermatoses, genodermatose en cocardes in 1947, clear cells acanthoma in1962 and especially malignant atrophiant papulosis (degos' disease) in 1942. http://www.bium.univ-paris5.fr/sfhd/biographies/degos_eng.htm
Extractions: Interne des Hôpitaux de Paris in 1926, Degos was appointed in 1934 as assistant at the Saint-Louis dermatological department headed by Gougerot, Professor of Dermatology whom he succeeded in 1951. For 25 years, Degos was fulfilling all the major responsabilities of French dermatology: General Secretary of the French Society of Dermatology, Professor of Dermatology, Chief Editor of the Annales de dermatology and author of a great textbook (Dermatologie) regarded as the bible of the french speaking dermatologists untill his last up-to-date edition in 1981. Degos described several dermatoses, genodermatose en cocardes in 1947, clear cells acanthoma in 1962 and especially malignant atrophiant papulosis (Degos' disease) in 1942. Back
Skin And Connective Tissue Diseases link/s Search PUBMED for Skin diseases All Review Therapy Diagnosis;degos' disease Malignant Atrophic Papulosis U. of Iowa; http://www.ohsu.edu/cliniweb/C17/C17.html
Dorlands Medical Dictionary degos' disease, syndrome (De·gos' disease, syndrome) (dschwagomacrz¢) Robertdegos, French dermatologist, born 1904 malignant atrophic papulosis. http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS
Extractions: Jean CIVATTE Robert Degos est et restera une des grandes figures de la dermatologie non seulement française mais mondiale: en ce dixième anniversaire de sa mort il n'est que juste de s'en souvenir. Une façon d'évoquer sa mémoire consiste à rappeler, sinon toutes, du moins les princiales affections qu'il a décrites ou dont il a précisé les cadres nosologiques. Certaines maladies portent à juste titre son nom. Cette évolution fatale est rapportée par les mêmes auteurs le 21 mai 1942 sous le titre "dermatite papulo-squameuse atrophiante (Epilogue)": cette appellation est donc, pour l'instant, conservée pour cette affection qui comporte les mêmes altérations histologiques sur la peau et l'intestin et qui fait discuter, mais pour l'éliminer, un lupus érythémateux aigu, en particulier du fait de l'absence de fièvre. En 1948, R.Degos,J.Delort et R.Tricot présentent devant la Société Médicale des Hôpitaux de Paris un travail sur ce même sujet avec, comme titre, "papulose atrophiante maligne (syndrome cutanéo-intestinal mortel)". Ils utilisent à nouveau ce nom, qui est désormains unaninement accepté, dans un article publié en 1952 dans les Annales de Dermatologie dans lequel ils rappellent leur observation, celle de Tzanck, Civatte et Sidi, et citent un cas présente en juin 1950 par F.P.Merklen et F.Cottenot qu'ils rapprochent du leur, mais sans l'y assimiler faute de renseignements suffisants. Depuis, le nom de maladie de Degos, ou Degos's disease ou syndrome dans la littérature anglo-saxonne, est adopté partout.
Segundo Ejemplar De La Revista Translate this page Malignant atrophic papulosis (degos' disease) involving three generationsof a family. Endoscopic and hystopatologic features of degos' disease. http://www.svcir.org/svc/revistas/5/Artic-2.html
D Disseminated Superficial Actinic Porokeratosis, 757335, 11. Donohue syndrome,259803, 5. Dowlingdegos´ disease, 9605, 2. Drug Eruption, 693010, 21. http://www.medik.sk/fotoar/koza/d.html
