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.

Author: Daramar Kitilar
Country: Iceland
Language: English (Spanish)
Genre: Technology
Published (Last): 19 October 2009
Pages: 118
PDF File Size: 16.64 Mb
ePub File Size: 13.59 Mb
ISBN: 324-6-57280-953-3
Downloads: 92844
Price: Free* [*Free Regsitration Required]
Uploader: Zulkimuro

May Pages ee22 Pages CiteScore measures average citations received per document published. 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.

Etiology The etiopathogenesis of the disease remains unknown. More developed lesions can imitate lichen sclerosus see this term. Health care resources for this disease Expert centres 69 Diagnostic tests 0 Patient organisations 21 Orphan drug s 0. Go to the members area of the website of the AEDV, https: Previous article Next article.

In the year has enfer,edad indexed in the Medlinedatabase, and has become a vehicle for expressing the most current Spanish medicine and modern. In early stages, histology of lesions may reveal a superficial and deep perivascular lymphocytic infiltration with distinct mucin deposition. Genetic counseling A genetic predisposition with an autosomal dominant trait has been suggested.

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

Face, scalp, palms of hands and soles of feet are rarely involved. From Monday to Friday from 9 a. Continuing navigation will be considered as acceptance of this use.

There was a problem providing the content you requested

Idiopathic, monosymptomatic, cutaneous presentations are benign, however, systemic fe can develop years after the occurrence of skin lesions. SRJ is a prestige metric based on the idea that not all citations are the same.

  ABB OD4110 PDF

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. It may more rarely manifest as pericarditis or in other organs such as the lungs, presenting as pleuritis. Other search option s Alphabetical list. Si continua navegando, consideramos que acepta su uso.

SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis degow diagnosis or treatment.

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.

Pemphigus Vegetans in the Inguinal Folds. The etiopathogenesis degoa the disease remains unknown. More developed lesions show prominent changes in the dermoepidermal junction, with atrophy of the epidermis and an area of sclerosis in the papillary dermis. Management and treatment 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.

If you are a member of the AEDV: Additional information Further information on this disease Classification s 3 Gene s 0 Clinical signs and symptoms Publications in PubMed Other website s 7.

Check this box if you wish to receive a copy of your message. This item has received. Systemic lesions may affect the gastrointestinal tract and the central detos system CNS and are potentially lethal.

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and enfdrmedad measure of the journal’s impact. You can change the settings or obtain more information by clicking here.

  BFY50 DATASHEET PDF

Later a wedge-shaped connective tissue necrosis in the deep dermis, due to a thrombotic occlusion of the small arteries and sparse lymphocytes, occurs. Diagnostic methods Diagnosis is based primarily on the cutaneous clinical picture that is nearly enfermfdad.

Print Send to a friend Export reference Mendeley Statistics. Differential diagnosis The histology of early lesions resembles cutaneous lupus erythematosus see this term. As all patients may potentially develop the systemic, life-threatening variant, an annual follow-up is mandatory.

Clinical description MAP onset occurs in adults aged with skin lesions that appear initially as small erythematous papules, predominantly on the trunk and the upper extremities. 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.

Degos disease – Wikidata

Read this article in English. Diagnosis is based primarily on the cutaneous clinical picture that is nearly pathognomonic. Subscribe to our Newsletter. The histology of early lesions degoss cutaneous lupus erythematosus see this term. Prognosis Idiopathic, monosymptomatic, cutaneous presentations are benign, however, systemic manifestations can develop years after the occurrence of skin lesions.

MAP onset occurs in adults aged with skin lesions that appear initially as small erythematous papules, predominantly on the degoos and the upper extremities.

Systemic manifestations are progressive and may lead to serious complications: This condition is chronic and lesions persist over years, often throughout life. Malignant atrophic papulosis MAP is a rare, chronic, thrombo-obliterative vasculopathy characterized by papular skin lesions with central porcelain-white deggos and a surrounding teleangiectatic rim.