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         Degos Disease:     more detail
  1. Case of the month. (Practice Trends).(diagnosing Degos' disease): An article from: Skin & Allergy News by Nancy Walsh, 2003-06-01
  2. Derm diagnosis.(Degos disease): An article from: Family Practice News by Nancy Walsh, 2003-06-01
  3. Textbook of Malignant Haematology by Laurent Degos, David C Linch, et all 1999-01-01
  4. Dermatologie (French Edition) by Robert Degos, 1976

81. Diseases Database Disease, Symptom, Sign, Etc Alphabetical Index : D Diseases Da
syndrome see Grey platelet syndrome Deflazacort Degenerative Degenerative disc diseasesee Intervertebral disc herniation degos' disease Dehydrated hereditary
http://www.diseasesdatabase.com/sieve/disease_index_d.asp
Diseases Database [Previous page] [Search] [Index] [Feedback]
Diseases Database disease, symptom, sign, etc alphabetical index : D
D-glycerate kinase deficiency
D-Glyceric aciduria see D-glycerate kinase deficiency
D-lactic acidosis

D-Moramide see Dextromoramide
see Stavudine
Dacarbazine

Daclizumab

Dacrocystitis
...
Dacryoadenitis

Dactinomycin see Actinomycin D
Dactylitis
Dactylolysis spontanea see Ainhum Dactylysis spontanea see Ainhum Dalmatian hypouricemia Dalteparin see Low molecular weight heparin Danaparoid sodium Danazol Dancing eyes-dancing feet syndrome see Opsoclonus myoclonus syndrome Dandruff see Seborrhoeic dermatitis Dandy-Walker syndrome Danon disease see Glycogenosis type 2b Danthron see Dantron Dantrolene Dantron Dapiprazole ... Dapsone Darbepoetin alfa see Erythropoietin Darier's disease see Keratosis follicularis (congenital) Darier's sign Darier-White disease see Keratosis follicularis (congenital) Darifenacin Daunorubicin Davidson disease see Congenital microvillous atrophy Dazoxiben DDAVP see Antidiuretic hormone DDC see Zalcitabine DDI see Didanosine de Grouchy syndrome type 1 see Deletion of short arm of chromosome 18 de Grouchy syndrome type 2 see Deletion of long arm of chromosome 18 De Lange syndrome de Morsier syndrome see Septo-optic dysplasia de Morsier-Gauthier syndrome see Kallmann syndrome De Quervain's tenosynovitis De Quervain's thyroiditis De Sanctis-Cacchione syndrome see Xeroderma pigmentosum group D de Vaal disease see Reticular dysgenesis Deafness see Hearing loss Dean-Barnes syndrome see Variegate porphyria Debrancher enzyme deficiency see Glycogenosis type 3 Debrisoquine Debrisoquine metabolism deficiency Decarboxycystine

82. Diseases Database Disease, Symptom, Sign, Etc Alphabetical Index : M Diseases Da
Male pattern baldness Male pseudohermaphroditism see Ambiguous genitalia (malegenotype) Malignant atrophic papulosis see degos' disease Malignant fibrous
http://www.diseasesdatabase.com/sieve/disease_index_m.asp
Diseases Database [Previous page] [Search] [Index] [Feedback]
Diseases Database disease, symptom, sign, etc alphabetical index : M
Machado-Joseph Azorean disease
Machupo virus see Bolivian hemorrhagic fever
MacLeod's syndrome

Macro-orchidism see Testicular enlargement
Macroamylasaemia

Macrocephaly see Megencephaly
Macrocytic red blood cell see Macrocytosis (erythrocyte)
Macrocytosis (erythrocyte)

Macroglossia

Macrogyria see Pachygyria
Macrolides
Macromastia see Breast hypertrophy Macroorchidism see Testicular enlargement Macrophage migration inhibitory factor Macrosomia Macrostomia ... Macrothrombocytosis Macular atrophy, Jadassohn type see Anetoderma Macular atrophy, Schweninger-Buzzi type see Anetoderma Macular hole Macular pucker see Epiretinal membrane Macular star see Hard retinal exudate Maculopapular rash Maculopathy Maculopathy, age related see Senile macular retinal degeneration Madelung's deformity Madura foot see Mycetoma Madurella mycetomi Mafenide Maffucci syndrome see Dyschondroplasia Magnesium hydroxide Magnesium levels low (plasma or serum) see Hypomagnesemia Magnesium levels raised (plasma or serum) see Hypermagnesaemia Magnesium oxide Magnesium salts Magnesium sulfate Maidenhair tree see Gingko biloba Majewski syndrome see Short rib-polydactyly syndrome type 2 Major histocompatibility complex class I deficiency Major tranquilizers see Antipsychotic agents Malabsorption syndrome Maladie de Roger Malakoplakia ... Malathion Malattia leventinese see Doyne's honeycomb choroiditis Malayan filariasis see Brugia malayi Male > Female see Incidence in males greater than females Male infertility Male pattern baldness Male pseudohermaphroditism

83. Roche Lexikon Medizin (4. Aufl.) - Degos*-Delort*-Tricot* Syndrom
Translate this page degos*-Delort*-Tricot* Syndrom. engl. degos' disease. Papulosis atrophicansmaligna. Verwandte Themen. Papulosis. Roche Lexikon Medizin
http://www.gesundheit.de/roche/ro05000/r7348.html
Degos*-Delort*-Tricot* Syndrom engl.: Degos' disease
Papulosis atrophicans maligna

Verwandte Themen Papulosis

84. Nature Publishing Group
References. 1 degos L. Do we treat a disease or a patient? A subtle differencewith dramatic consequences. The Hematology Journal 1 2 71, 2000; MEDLINE.
http://www.nature.com/cgi-taf/DynaPage.taf?file=/thj/journal/v2/n3/full/6200109a

85. Zebra Card TH-011: Axillary Freckling
(), Ultrastructure of early pigmentary changes in Dowling-degos' disease.Grosshans E, Geiger JM, et al. J Cutan Pathol 1980 Apr;7(2)77-87.
http://www.zebracards.com/TH-011.html
Zebra Cards Update Thorax
TH-011 Nav Axillary freckling Differential Diagnosis Top Nav neurofibromatosis 1 Discussion not available online Top Nav Erratum in printed version Top Nav Last page of the article in Arch Dis Child is 307, not 310. Update Comments Top Nav
  • Incorrectly identifies inguinal freckling as the Crowe sign. Crowe briefly mentions perineal freckling in his paper, but never inguinal freckling. [
  • Briefly discusses two rare forms of neurofibromatosis that involve mosaicism. A parent may have the NF mutation only in cells of his or her germ line, and, because of this mosaicism, appear clinically unaffected. Similarly, the NF mutation may occur during embryogenesis, so only a portion of the patient's body is affected. This is most easily noticed in diseases with cutaneous manifestations, such as neurofibromatosis 1. [
  • There is another condition in which skin pigmentation may change with stress. Patients with Addison disease lose the hyperpigmentation characteristic of that disorder because of their equally characteristic edema. The pigmentation rapidly reappears, however, when they become dehydrated with the onset of an Addisonian crisis. [p. 94] [
Footnotes in Print Edition Top Nav Axillary freckling as a diagnostic aid in neurofibromatosis.

86. Skin Signs Of Systemic Disease
diethylstilbestrol, and isoniazid (INH). Differential diagnosis confluentand reticulated papillomatosis, Dowlingdegos' disease;
http://www.clevelandclinicmeded.com/diseasemanagement/dermatology/skinsigns/skin
Published July 1, 2002
Sharon J.
Longshore, MD
Department of
Dermatology
Kenneth J.
Tomecki, MD
Department of
Dermatology
Print Chapter
The Cleveland Clinic Foundation The skin is often a window to systemic disease. By appreciating cutaneous manifestations of systemic diseases the internist can better determine the appropriate diagnosis, therapy, or need for referral to a dermatologist. This chapter contains a concise review of common dermatoses and cutaneous disorders specific to the subspecialties of internal medicine. In each section a brief description of the disorder is followed by an abbreviated list of differential diagnoses and therapeutic options.
Common Benign
Cutaneous Disorders
Skin Disease and Internal Cancer
Skin Diseae and Cardiovascular Disease ...
References
COMMON BENIGN
CUTANEOUS DISORDERS Seborrheic dermatitis (Figure 1)
is a common, chronic, superficial inflammatory disease of the scalp, face, and central chest. Erythematous, often greasy, plaques favor hair-bearing areas. Pruritus of the scalp is common. Disease in infants is commonly known as cradle cap.

87. FSU College Of Medicine - Vision
In the late twentieth century, the welltrained physician is equipped to treat degos’disease but not shoulder pain, eosiniphilic fasciitis but not the much
http://med.fsu.edu/vision.asp
Select One About the College Administration Blackboard Calendar Departments Health Affairs Medical Library Meet the Faculty Medical Education Regional Campuses Student Life Home Search: About the College Mission Vision History ... Directions
Vision
The FSU College of Medicine will lead the nation in preparing compassionate physicians to deliver the highest quality 21st Century patient-centered medicine to communities of greatest need.
THE FUTURE OF MEDICAL EDUCATION:
THE FLORIDA STATE UNIVERSITY
COLLEGE OF MEDICINE Myra M. Hurt, Ph.D.
Associate Dean, College of Medicine
Preamble In an article from the New England Journal of Medicine entitled The Ecology of Medical Care written by a group of researchers in the departments of Preventative Medicine, Medicine, and Biostatistics at the University of North Carolina, the following is reported: in a population of 1000 adults (age sixteen or older), 750 will experience an episode of illness in a particular month; of these, 250 will consult a physician; 9 of these will be hospitalized, and 1 will be referred to a university medical center. The focus of medical textbooks is that 1 case (in the metaphorical sense) that makes to it to the university medical center. The year the article was written was 1961 (NEJM, 1961, 265:885). The focus of medical education in academic medical centers today is largely the same.

88. Untitled
Included in Series 4 are research materials on diabetes and skin diseases associatedwith diabetes, including degos' disease, necrobiosis lipoidica diabeticorum
http://www.collphyphil.org/FIND_AID/hist/histgwb1.htm
MSS 2/0257-01 Acc. 1992-039 BINKLEY, GEORGE W. (1904-1974) Papers, 1930-1974 Biographical George Webster Binkley, dermatologist and Professor of Dermatology, was born in Canton, Ohio, on 24 January 1904. He was the son of Emmaus Arthur and Della Baker Binkley. In 1930, he married Kathryn Sensenig. Binkley died in Hendersonville, North Carolina, on 2 April 1974. George W. Binkley graduated from the Western Reserve University School of Medicine in 1930. He interned at St. Luke's Hospital in Cleveland and at Highland Hospital in Oakland, California, from 1931 to 1932. In 1933, Binkley began a residency in dermatology at University Hospitals in Cleveland and at Cleveland City Hospital. In 1937, after completing his residency, Binkley began a private practice and became an instructor in Dermatology at Western Reserve University School of Medicine. Eventually, Binkley became Professor of Dermatology and Syphilology and in 1970 became Professor Emeritus of Dermatology. In addition, Binkley served as a consultant at several hospitals in Cleveland, including University Hospitals, Rainbow Hospital, and Benjamin Rose Hospital. Binkley, who specialized in skin diseases associated with diabetes, published numerous articles and contributed a chapter to Diabetes Mellitus: Theory and Practice (1970). He was a member of numerous medical and dermatological societies, including the American Dermatological Association, the American Academy of Dermatology, and the American Society of Dermatopathology. Binkley also was a member of the Cleveland Dermatological Society and at one time served as president of this organization. Scope and contents The papers of George W. Binkley, spanning 1930 to 1974, document his career as a dermatologist, professor, and frequent contributor to dermatological publications; the collection also provides evidence of Binkley's special interest in skin diseases associated with diabetes. Included in the collection are personal papers, correspondence, records of Binkley's involvement in various professional organizations, his research materials on diabetes, and samples of his essays and speeches. Series 1 contains Binkley's personal papers; present are records of his military service, certifications by various medical boards, and faculty and hospital appointments. Also present is Binkley's curriculum vitae, his bibliography, biographical information, and miscellaneous certificates. Binkley's correspondence is contained in Series 2. Present are incoming letters and autograph drafts or carbon copies of Binkley's outgoing letters. Included are requests for reprints, permissions to use photographs, and correspondence with various medical journals. Binkley corresponded with other dermatologists and often made queries about their research findings and theories; correspondents include dermatologists Alfred W. Kopf, Raul Fleischmajer, J. E. Jelinek, and Beno Michel. Series 3 contains materials pertaining to Binkley's membership in various professional organizations. Included are records of Binkley's involvement in the Division of Education and Communication (DECOM) of the American Academy of Dermatology's National Program for Dermatology. Present are meeting agendas, summaries of projects, memoranda, correspondence, and a roster of task forces. Also welldocumented is Binkley's participation in four annual meetings (1970-1973) of the American Society of Dermatopathology; present are programs, registration information, membership rosters, by laws, correspondence, abstracts of papers, and notes taken by Binkley at presentations. Included in Series 4 are research materials on diabetes and skin diseases associated with diabetes, including Degos' Disease, necrobiosis lipoidica diabeticorum, scleredema, and idiopathic hemochromatosis. Present are clippings, essays, and reprints of articles, all of which are heavily annotated by Binkley. Also present are Binkley's notes, correspondence, bibliographies, case studies, and photographs. Binkley might have assembled these materials while researching and preparing to write his chapter on "Skin in Diabetes" in Diabetes Mellitus: Theory and Practice. Works on dermatology, by Binkley and Herbert Z. Lund, are contained in Series 5. Present are essays by Binkley and materials relating to "Skin in Diabetes", his contribution to Diabetes Mellitus: Theory and Practice, edited by Max Ellenberg and Harold Rifkin. Included is correspondence with Ellenberg and Rifkin about the publication of the book, and drafts and page proofs of Binkley's chapter. Also present are two printed works by Lund: Tumors of the Skin (1957) and Melanotic Tumors of the Skin (1961). Binkley has annotated both works. Provenance The papers of George W. Binkley were donated to the Historical Collections of the Library of the College of Physicians of Philadelphia by his wife, Kathryn S. Binkley, on 8 August 1974. The collection was processed and catalogued in 1992. 1930-1974 3 boxes and 1 oversize folder (1.25 linear ft.) 4/27/1992 wvg MSS 2/0257-01 Acc. 1992-039 BINKLEY, GEORGE W. (1904-1974) Papers, 1930-1974 Box Ser. 1 1 PERSONAL PAPERS, 1930-1974. 1. Military service 1930 Jan. 21-1953 May 1 (1 folder) 1930-1953 2. Graduation program and alumni certificate 1930 June 12 (1 folder) 1930 OV 3. Ohio State Medical Board Certificate 1930 July 8 (1 folder) 1930 4. Certification information 1. California Board of Medical Examiners 1932-1967 (1 folder) 1932-1967 2. Ohio State Medical Board 1969-1970 (1 folder) 1969-1970 3. North Carolina Board of Medical Examiners 1970-1974 (1 folder) 1970-1974 5. Faculty and hospital appointments 1. Correspondence 1933 Mar. 30-1968 July 1 (1 folder) 1933-1968 2. Forms 1951 Jan. 29-1973 May 1 (1 folder) 1951-1973 6. Miscellaneous certificates 1935 July 1-1942 Jan. 30 (3 folders) 1935-1942 7. Curriculum vitae and biographical information 1940 Apr. 3-1973 Apr. (1 folder) 1940-1973 8. Proofs from medical directories 1945-1961 (1 folder) 1945-1961 9. Bibliography 1955 Jan. (1 folder) 1955 10. Clippings and notes on pollution 1970 (1 folder) 1970 2 CORRESPONDENCE, 1947-1973. 1. 1947 Apr. 16-1959 Feb. 25 (1 folder) 1947-1959 2. 1960 Apr. 29-1970 May 13 (2 folders) 1960-1970 3. 1965 Jan. 25-1968 May 20 (1 folder) 1965-1968 4. 1970 Jan. 14-1973 May 8 (2 folders) 1970-1973hBox Ser. 1 3 PROFESSIONAL ORGANIZATIONS, 1937-1974. 1. American Medical Association 1. Membership cards 1950, 1970-1974 (1 folder) 1950-1974 2. Memorial to H. N. Cole 1966 Oct. 11 (1 folder) 1966 3. Miscellaneous 1937-1971 (1 folder) 1937-1971 2. American Dermatological Society Membership information 1948 May 14-1970 (1 folder) 1948-1970 2 3. Academy of Medicine of Cleveland Membership information and constitution and by laws 1954-1973 (1 folder) 1954-1973 4. American Academy of Dermatology 1. Correspondence and membership information 1969 June 20-1974 (1 folder) 1969-1974 2. Reports of National Program for Dermatology 1971 Summer 1972 Spring (1 folder) 1971-1972 3. Division of Education and Communication (DECOM) 1971 Dec. 10-1973 Sept. 11 (1 folder) 1971-1973 5. American Society of Dermatopathology 1. Annual meeting, 1970 1968 Nov. 1-1970 Dec. 4 (1 folder) 1968-1970 2. Annual meeting, 1971 1971 June 8-Dec. 3 (1 folder) 1971 3. Annual meeting, 1972 1972 Feb. 28-Dec. 3 (1 folder) 1972 4. Annual meeting, 1973 1973 Apr. 19-Dec. 6 (1 folder) 1973 6. Ohio State Medical Association Membership cards and correspondence 1971-1973 (1 folder) 1971-1973 Box Ser. 2 4 DIABETES RESEARCH, 1939-1971. 1. Diabetes mellitus 1939-1971 (6 folders) 1939-1971 2. Malignant atrophic papulosis (Degos' Disease) 1942-1970 (3 folders) 1942-1970 3. Necrobiosis lipoidica diabeticorum (N.L.D.) 1948-1966 (1 folder) 1948-1966 3 4. Scleredema 1961-1969 (3 folders) 1961-1969 5. Idiopathic hemochromatosis 1967-1968 (1 folder) 1967-1968 6. Miscellaneous 1960-1968 (2 folders) 1960-1968 5 WORKS ON DERMATOLOGY, 1938-1970. 5.1 Works by Binkley 1. Miscellaneous essays and speeches 1938 Oct. 31 and [n.d.] (1 folder) 1938 2. "Skin in Diabetes" (Binkley's chapter in Diabetes Mellitus: Theory and Practice) 1. Correspondence 1967 May 15-1971 Jan. 13 (1 folder) 1967-1971 2. Typescript drafts 1968 Apr. 1970 Nov. (2 folders) 1968-1970 3. Page proofs [ca. 1971] (1 folder) [ca.1971] 5.2 Works by Herbert Z. Lund 1. Tumors of the Skin by Herbert Z. Lund 1957 Oct. (1 folder) 1957 2. Melanotic Tumors of the Skin by Herbert Z. Lund and Jane Merrill Kraus 1961 Nov. (3 folders) 1961 1930-1974 3 boxes and 1 oversize folder (1.25 linear ft.) 4/27/1992 wvg

89. Skin Signs And Systemic Disease - Information For Patients
Home Patient information Skin signs and systemic disease. Skinsigns and systemic disease. The skin may reflect signs of systemic
http://www.dermnetnz.org/contents/systemic.html
Home Patient information
Skin signs and systemic disease
The skin may reflect signs of systemic diseases, useful for diagnosis, or suffer from a complication of disease or its treatment. Here are links to pages about the dermatological manifestations of non-infectious internal diseases: immune, autoimmune and rheumatic diseases; genetic, metabolic, endocrine and nutritional states; internal malignancy; haematological diseases; and drug eruptions. Acute febrile neutrophilic dermatosis
Angioedema

Behcet's disease

Chilblains
...
Xeroderma pigmentosum

If you have any concerns with your skin or its treatment, see a dermatologist for advice.
New Zealand Dermatological Society.
Last updated 30 March 2003.

90. 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

91. 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

92. EmailPinoy Web Directory
13); Klinefelter Syndrome@ (13); KluverBucy Syndrome@ (3); Kohlmeier-Degosdisease@ (4); Krabbe disease@ (3). Conditions and diseases
http://search.emailpinoy.com/cgi-bin/webpod.cgi/Health/Conditions_and_Diseases/K
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  • 93. SpringerLink: Der Hautarzt - Abstract Volume 52 Issue 8 (2001) Pp 734-737
    Translate this page A 71-year-old male patient presented with malignant atrophic papulosis (Köhlmeier-Degosdisease). He developed multiple distinctive cutaneous lesions.
    http://link.springer-ny.com/link/service/journals/00105/bibs/1052008/10520734.ht
    Der Hautarzt
    ISSN: 0017-8470 (printed version)
    ISSN: 1432-1173 (electronic version) Table of Contents Abstract Volume 52 Issue 8 (2001) pp 734-737
    farbbildkasuistik
    Diagnose, Therapie, Verlauf
    C. Vicktor, U. Schultz-Ehrenburg
    Dermatologische Klinik des Klinikum Buch, Berlin
    Zusammenfassung Abstract Keywords Article in PDF format (179 KB) Online publication: July 25, 2001
    SpringerLink Helpdesk

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