ENFERMEDAD DE DEGOS PDF

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 aƱos y vivo en Madrid y me diagnoticaron la enfermedad de Degos en despues de que perdiera la vision del ojo.

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More developed lesions show prominent changes in the dermoepidermal junction, with atrophy of the epidermis and an area of sclerosis in the papillary dermis.

Check this box if you wish to receive a copy of your message. Many patients have been reported to have defects in blood coagulation. MAP onset occurs in adults aged with skin lesions that appear initially as small erythematous papules, predominantly on the trunk and the upper extremities.

Degos disease – Wikidata

Differential diagnosis The histology of early lesions resembles cutaneous lupus erythematosus see this term. Additional information Further information on this regos Classification s 3 Gene s 0 Clinical signs and symptoms Publications in PubMed Other website s 7. Show more Show less.

Later a wedge-shaped connective tissue necrosis in the deep dermis, due to a thrombotic occlusion of the small arteries and sparse lymphocytes, occurs. Prognosis Idiopathic, monosymptomatic, cutaneous presentations are benign, however, systemic manifestations can develop years after the occurrence of skin lesions.

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Are you a health professional able to prescribe or dispense drugs? Continuing navigation will be considered as acceptance of this use. Subscriber If you already have your login data, please click here. Over several days, the center of the lesions sinks and develops a characteristic morphology: Pemphigus Vegetans in the Inguinal Folds.

Systemic manifestations are progressive and may lead to serious complications: Si continua navegando, consideramos que acepta su uso. Face, scalp, palms of hands and soles of feet are rarely involved. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

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Hypotheses implicating vasculitis, coagulopathy or a primary dysfunction of endothelial cells have been proposed. Ocular involvement, which affects the eyelids, conjuctiva, retina, sclera and the choroid plexus, as well as the development of diplopia and ophthalmoplegia as secondary side effects of the neurologic involvementhas also been described. For all other comments, please send your remarks via contact us. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences ve the analyses dnfermedad navigation customer behavior.

It may more rarely manifest as pericarditis or in other organs such as the lungs, presenting as pleuritis. Degks condition is chronic and lesions persist over years, often throughout life.

enfermedad de degos

Diagnostic methods Diagnosis is based primarily on the cutaneous clinical picture that is nearly pathognomonic. The documents contained in this web site are presented for information purposes only.

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Systemic lesions may affect the gastrointestinal tract and the central nervous system CNS and are potentially lethal. Specialised Social Services Eurordis directory. Go to the members area of the website of the AEDV, https: May Pages ee22 Pages Read this article in English. Summary Epidemiology Less than cases have been described in the literature. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.

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From Monday to Friday from 9 a. If you are a member of the AEDV: As all patients may potentially develop the degoe, life-threatening variant, an annual follow-up is mandatory.

Print Send to a friend Export reference Mendeley Statistics. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

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. All articles are subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style. The histology of early lesions resembles cutaneous lupus erythematosus see this term.