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61. Köhlmeier - Degos Disease
Köhlmeier Degos disease. Malignant Atrophic Papulosis. Pericarditis, pleuraleffusions; Restrictive pulmonary disease; Cerebral edema, increased ICP.
http://www.gasnet.org/pda/pediatric-syndromes/kohlmeier-degos.html
Malignant Atrophic Papulosis
  • Occlusive vasculitis Multiple cutaneous, GI, CNS infarcts Porcelain papules with atrophic scaring Pericarditis, pleural effusions Restrictive pulmonary disease Cerebral edema, increased ICP
Introduction Contents

62. Baylor Neurology Case Of The Month
CVT), Wegener s granulomatosis, Cogan s syndrome, kohlmeierdegos syndrome, systemiclupus erythematosus, polyarteritis nodosa, sarcoidosis, Crohn’s disease.
http://www.bcm.tmc.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

63. 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 this article,
http://www.amershamhealth.com/medcyclopaedia/medical/Volume IV 1/KOHLMEIER DEGO
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Kohlmeier degos disease, rare vasculitis characterized by skin lesions as well as malabsorption, bowel ischaemia and perforation.
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The Encyclopaedia of Medical Imaging Volume IV:1
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64. Browse By Letter 'K'
smlaigne syndrome Kocher lorenz fracture Koerner s septum Kohler s disease (VOLUMEIII 1) Kohler s disease (VOLUME VII) Kohlmeier degos disease Kohn, pores of
http://www.amershamhealth.com/medcyclopaedia/medical/indexk.asp
Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Entry words starting with K
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K edge

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65. Degos Patients Support Network Website | Information | For Professionals
Barabino A, Pesce F, Gatti R An atypical paediatric case of malignantatrophic papulosis (Kohlmeier Degos disease). Eur J Pediatr
http://www.degosdisease.com/information/forpros/diagnosing-degos/synonyms_relate
Special Concerns:
  • Patients with isolated skin lesions may develop systemic disease after many years and should receive regular follow-up care. Aizawa H, Takase Y, Inoue K: [An autopsy case of Degos disease with neurological symptoms neuropathological observations and increased platelet aggregation]. Rinsho Shinkeigaku 1992 Jan; 32(1): 23-9 [Medline]
  • Assier H, Chosidow O, Piette JC: Absence of antiphospholipid and anti-endothelial cell antibodies in malignant atrophic papulosis: a study of 15 cases. J Am Acad Dermatol 1995 Nov; 33(5 Pt 1): 831-3 [Medline]
  • Atchabahian A, Laisne MJ, Riche F: Small bowel fistulae in Degos' disease: a case report and literature review. Am J Gastroenterol 1996 Oct; 91(10): 2208-11 [Medline]
  • Barabino A, Pesce F, Gatti R: An atypical paediatric case of malignant atrophic papulosis (Kohlmeier- Degos disease). Eur J Pediatr 1990 Apr; 149(7): 457-8 [Medline]
  • Barlow RJ, Heyl T, Simson IW: Malignant atrophic papulosis (Degos' disease)diffuse involvement of brain and bowel in an African patient. Br J Dermatol 1988 Jan; 118(1): 117-23 [Medline]
  • Barriere H: [Malignant atrophying papulosis (Degos' disease) (author's transl)]. Ann Dermatol Venereol 1978 Aug-Sep; 105(8-9): 733-9

66. K In Health > Conditions And Diseases
Klinefelter Syndrome@ (12); KluverBucy Syndrome@ (4); Kohlmeier-Degosdisease@ (5); Krabbe disease@ (3). This category in other languages
http://ilectric.com/glance/Health/Conditions_and_Diseases/K/
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67. EMedicine - Malignant Atrophic Papulosis : Article Excerpt By: Hemant Pande, MD
Synonyms, Key Words, and Related Terms MAP, kohlmeierdegos syndrome, Degosdisease, vascular occlusive disorders, thromboangiitis obliterans.
http://www.emedicine.com/med/byname/malignant-atrophic-papulosis.htm
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Excerpt from Malignant Atrophic Papulosis
Synonyms, Key Words, and Related Terms: MAP, Kohlmeier-Degos syndrome, Degos disease, vascular occlusive disorders, thromboangiitis obliterans
Please click here to view the full topic text: Malignant Atrophic Papulosis
Background: Kohlmeier described a case of malignant atrophic papulosis (MAP) as a form of thromboangiitis obliterans in 1941. It was recognized as a distinct clinical entity by Degos in 1942, hence the name. Pathophysiology: MAP is a multisystem disorder involving the small-caliber blood vessels. The disease 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. MAP is different from other vasculitides in that inflammation is not a prominent component of the disease. MAP may involve the gastrointestinal and genitourinary tracts, central and peripheral nervous systems, skin, heart, lungs, eyes, pancreas, adrenals, and kidneys. The disease involves the skin alone in 37% of cases. The gastrointestinal tract is involved in about 50% of cases. Frequency:
  • Internationally: This is a rare disease, with fewer than 150 cases reported. Most of the cases are sporadic, although members of the same family reportedly have been affected.

68. :: Ez2Find :: Degos
Disorders (354) Web Sites, Degos disease Site Info - Translate- Open New Window Email group to share information and support.
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69. Sjukdom, Sjukdomslista På Engelska, Michel Tandläkare Ta Hand Om Dig
KleineLevin Syndrome. Kleptomania. Klinefelter Syndrome. Kohlmeier Degos disease.Krabbe disease. L. Lactose Intolerance. Langer-Giedion Syndrome. Laryngitis.
http://www26.brinkster.com/privtand/sjuk.htm
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70. Malabsorption Syndromes
develop. Whipple s disease; Lymphoma4. Kohlmeier Degos (primary progressivearterial occlusive disease). E. Cardiovascular disorders
http://enotes.tripod.com/malabsorption.htm
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TOC
GI MALABSORPTION SYNDROMES Suspected in pts with persistent weight loss despite a more than adequate caloric intake. A. Inadequate digestion
  • Postgastrectomy steaorrhea
  • Deficiency or inactivation of pancreatic lipase
    a. Exocrine pancreatic insufficiency (1) Chronic pancreatitis (2) Pancreatic carcinoma (3) Cystic fibrosis (4) Pancreatic resection
    b. Ulcerogenic tumor of the pancreas (Zollinger Ellison syndrome) B. Reduced intestinal bile salt concentration
  • Liver disease
    a. Parenchymal liver disease b. Cholestases (intrahepatiac or extrahepatic)
  • Abnormal bacterial proliferation in the small bowel
    a. Afferent loop stasis b. Strictures c. Fistula d. Blind loops e. Multiple diverticula of the small bowel f. Hypomotility states (diabetes, scleroderma; intestinal pseu obstruction
  • Interrupted enterohepatic circulation of bile salts a. Ileal resection b. Ileal inflammatory disease (Crohn's regional ileitis)
  • Drug induced (by sequestration or precipitation of bile salts) a. Alcohol b. Cholestyramine c. Calcium carbonate d. Neomycin
  • 71. Fablis Directory For /Health/Conditions_and_Diseases/K
    KleineLevin Syndrome@; Kleptomania@; Klinefelter Syndrome@; Kohlmeier-Degosdisease@; Krabbe disease@. This category needs an editor.
    http://directory.fablis.com/guide/Health/Conditions_and_Diseases/K
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    72. Wuup.de - /Health/Conditions_and_Diseases/K
    Kohlmeier-Degosdisease@; Krabbe disease@. Letztes Update 2003-11-04 115949.
    http://wuup.de/index.php/Health/Conditions_and_Diseases/K

    73. Degos From Linkspider UK Health Directory
    Degos disease Personal account and message board. Doctor s DoctorDegos disease - Synonyms, appearance and prognosis. Degos disease
    http://linkspider.co.uk/Health/ConditionsandDiseases/RareDisorders/Degos/
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    74. Directory
    KleineLevin Syndrome@; Kleptomania@; Klinefelter Syndrome@; Kohlmeier-Degosdisease@; Krabbe disease@. Search K at Juppyn Search Search
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    75. K Search, K Sites At B2bYellowpages.com
    Klinefelter Syndrome@ (12); KluverBucy Syndrome@ (4); Kohlmeier-Degosdisease@ (4); Krabbe disease@ (3). This category in other languages
    http://b2byellowpages.com/web.cgi/Health/Conditions_and_Diseases/K/
    Find search results for K at b2bYellowpages.com. Your K source. List Your Business Advertising Sponsorships Needs and Leads ... Log in ACCURATE WEB SEARCH:
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  • 76. Publications Of Dr Björck
    Bjorck S, Johansson SL, Aurell M. Acute renal failure caused by a rapidlyprogressive arterioocclusive syndromeKohlmeier-Degos disease?
    http://kidney.med.gu.se/Ref/Bjorck.htm
    Staffan Björck
    Bjorck S, Blohme G. Tidig behandling kan forbattra prognos vid diabetisk njursjukdom. Lakartidningen 1998; 95(47):5326-8 5333-4. English title: "Early treatment can improve prognosis in diabetic nephropathy" Prognosis in diabetic nephropathy has changed dramatically during the past decade, and slowing of the disease process has been made possible by intervention against specific risk factors. Nonetheless, diabetic nephropathy has become the leading cause of end stage renal disease. Early detection and prevention, or at least delaying, of disease progression have become crucial aims, and several treatment strategies designed to prevent end stage renal disease have recently been published. The common denominator of these strategies is screening for microalbuminuria in diabetic patients rather than awaiting the appearance of overt symptoms. (Lipids);

    77. Conditions And Diseases / K
    disease. KleineLevin Syndrome, Klinefelter Syndrome, Kohlmeier-Degosdisease. Help build the largest human-edited directory on the web.
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    78. Health: Conditions And Diseases: K
    Klinefelter Syndrome@ (12); KluverBucy Syndrome@ (4); Kohlmeier-Degosdisease@ (5); Krabbe disease@ (3). Warning fopen(http//205.209
    http://www.nebulasearch.com/directory/go/Health/Conditions_and_Diseases/K/
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  • 79. ILDS - ICD10
    ICD Code, Disorder. I74.410 Embolism, arterial. I77.800 Kohlmeier Degos syndrome. I80.810Mondor s disease. I80.810 Sclerosing periphlebitis of chest wall.
    http://web.ilds.org/icd10_list.php?VIEW=1&START_CODE=I74.4&START_EXT=10

    80. Katalog :  : Health : Conditions_and_Diseases : K :  - Netz-Tipp.De
    disease (*). This category in otherlanguages Danish, Dutch, German. Spanish. Jetzt chatten! Klick!
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