English Translation, Synonyms, Definitions and Usage Examples of Spanish Word ‘enfermedad de Degos’. Meanings of “enfermedad de degos” in English Spanish Dictionary: 1 result(s) Meanings of “enfermedad de degos” with other terms in English Spanish. Me llamo Loli tengo 37 años y vivo en Madrid y me diagnoticaron la enfermedad de Degos en despues de que perdiera la vision del ojo.
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Malignant atrophic papulosis MAP is a rare, chronic, thrombo-obliterative vasculopathy characterized by papular skin lesions with central porcelain-white atrophy and a surrounding teleangiectatic rim. SRJ is a prestige metric based on the idea that not all citations are the same. Subscriber If you already have your login data, please click here. Diagnosis is based primarily on the cutaneous clinical picture that is nearly pathognomonic.
More developed lesions can imitate lichen sclerosus see this term. CiteScore measures average citations received per document published. Read this article in English.
Prognosis Idiopathic, monosymptomatic, cutaneous presentations are benign, however, systemic manifestations can develop years after the occurrence of skin lesions. Systemic lesions may affect the gastrointestinal tract and the central nervous system CNS and are potentially lethal.
Go to the members area of the website of the AEDV, https: Genetic counseling A genetic predisposition with an autosomal dominant trait has been suggested.
enfermedad de Degos – English Translation – Word Magic Spanish-English Dictionary
Previous article Next article. In early stages, histology of lesions may reveal a superficial and deep perivascular lymphocytic infiltration with distinct mucin deposition. Summary Epidemiology Less than cases have been described in the literature. Systemic manifestations are progressive and may lead to serious complications: The etiopathogenesis of the disease remains unknown. Etiology The etiopathogenesis of the disease remains unknown.
Therapeutic efforts with anticoagulants and compounds that facilitate blood perfusion, such as acetylosalicylic acid, pentoxifylline, dipyridamole, ticlodipine and heparin have achieved a partial regression of skin lesions in some individual cases. You can change the settings or obtain more information by clicking here.
Subscribe to our Newsletter. Continuing navigation will be considered as acceptance of this use. The histology of early lesions resembles cutaneous lupus erythematosus see this term. From Monday to Friday from 9 a. Are you a health professional able to prescribe ddegos dispense drugs?
All articles are subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style. Diagnostic methods Diagnosis is based primarily on the cutaneous clinical picture that is nearly pathognomonic.
Summary and related texts. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.
The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a degis for diagnosis or treatment. Additional information Further information on this disease Classification s 3 Gene s 0 Clinical signs and symptoms Publications in PubMed Other website s 7. If you are a member of the AEDV: SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.
MAP onset occurs in adults aged with skin lesions that appear initially as small erythematous papules, predominantly on the trunk and the upper extremities.
To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. A clinical inspection of the skin should be combined with additional examinations including brain magnetic resonance tomography, gastroscopy, colonoscopy, X-ray of the chest and abdominal ultrasound, in order to assess the long-term prognosis. SJR uses a snfermedad algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.
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Check this box if you wish to receive a copy of your message. Many patients have been reported to have defects in blood coagulation. As all patients may enffermedad develop the systemic, life-threatening variant, an annual follow-up is mandatory.
Idiopathic, monosymptomatic, cutaneous presentations are benign, however, systemic manifestations can develop years after the occurrence of skin lesions. It may more rarely manifest as pericarditis or in other organs such as the lungs, presenting as pleuritis.
Print Send to a friend Export reference Mendeley Statistics. Specialised Social Services Eurordis directory. Face, scalp, palms of hands and soles of feet are rarely involved.
Pemphigus Vegetans in the Inguinal Folds.
Enfermedad de Degos
More developed lesions show prominent changes in the dermoepidermal junction, with atrophy of the epidermis and an area of sclerosis in the papillary dermis. This item has received.
Disease definition Malignant atrophic papulosis MAP is a rare, chronic, thrombo-obliterative vasculopathy characterized by papular skin lesions with central porcelain-white atrophy and a surrounding teleangiectatic rim. Over several days, the center of the lesions sinks and develops a characteristic morphology: Other search option s Alphabetical list. This condition is chronic and lesions persist over years, debos throughout life. Differential diagnosis The histology of early lesions resembles cutaneous lupus erythematosus see this term.