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 can imitate lichen sclerosus see this term. If you are a member of the AEDV: Differential diagnosis The histology of early lesions resembles cutaneous lupus erythematosus see this term. 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.

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Degos disease – Wikidata

Subscriber If you already have your login data, please click here. Clinical description MAP onset occurs in adults aged with skin lesions that appear initially as small erythematous papules, predominantly on the trunk and the enermedad extremities. Disease definition Malignant atrophic papulosis MAP is a rare, chronic, thrombo-obliterative vasculopathy characterized by papular skin lesions with central dgos atrophy and a surrounding teleangiectatic rim.

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In the year has been indexed in the Medlinedatabase, and has become a vehicle for expressing the most current Spanish medicine and modern.

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Idiopathic, monosymptomatic, cutaneous presentations are benign, however, systemic manifestations can develop years after the occurrence of skin lesions. No effective treatment for the systemic manifestations has been established, however, subcutaneous treprostinil has been tested successfully in one case with intestinal and CNS manifestations.

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enfermedad de degos

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. This condition is degox and lesions persist over years, often throughout life. Si continua navegando, consideramos que acepta su uso. Check this box if you wish to receive a copy of your message.

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Many patients have been reported to have defects in blood coagulation. 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.

Face, scalp, palms of hands and soles of feet are re involved.

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MAP onset occurs in adults aged with skin lesions that appear initially as efnermedad erythematous papules, predominantly on the trunk and the upper extremities. Later a wedge-shaped connective tissue necrosis in the deep dehos, due to a thrombotic occlusion of the small arteries and sparse lymphocytes, occurs. The degks contained in this web site are presented for information purposes only. Other search option s Alphabetical list. Over several days, the center of the lesions sinks and develops a characteristic morphology: Systemic lesions may affect the gastrointestinal tract and the central nervous system CNS and are potentially lethal.

Print Send to a friend Export reference Mendeley Statistics. More developed lesions show prominent changes in the dermoepidermal junction, with atrophy of the epidermis and an area of sclerosis in the papillary dermis. The etiopathogenesis of the disease remains unknown.

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It may more rarely manifest as pericarditis or in other organs such as the lungs, presenting as pleuritis. This item has received.

SRJ is a prestige metric based on the idea that not all citations are the same. Diagnosis is based primarily on the cutaneous clinical picture that is nearly pathognomonic.

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

In early stages, histology of lesions may reveal a superficial and deep perivascular lymphocytic infiltration with distinct mucin deposition. Systemic manifestations are progressive and may lead to serious complications: Diagnostic methods Diagnosis is based primarily on the cutaneous clinical picture that is nearly pathognomonic.

Enfermedad de Degos

Go to the members area of the website of the AEDV, https: Degoa implicating vasculitis, coagulopathy or a primary dysfunction of endothelial cells have been proposed. Only comments written in English can be processed. Show more Show less. Subscribe to our Newsletter. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Etiology The etiopathogenesis of the disease remains unknown.