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: Akinojar Shaktigrel
Country: Mauritania
Language: English (Spanish)
Genre: Career
Published (Last): 27 July 2007
Pages: 42
PDF File Size: 4.4 Mb
ePub File Size: 19.76 Mb
ISBN: 151-9-96022-852-3
Downloads: 2322
Price: Free* [*Free Regsitration Required]
Uploader: Dajora

Hypotheses implicating vasculitis, coagulopathy or a primary dysfunction of endothelial cells have been proposed. More ds lesions can imitate lichen sclerosus see this term. Print Send to a friend Export reference Mendeley Statistics. 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.

In early stages, histology of lesions may reveal a superficial and deep perivascular lymphocytic infiltration with enfermecad mucin deposition. Diagnosis is based primarily on the cutaneous clinical picture that is nearly pathognomonic. 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.

Term Bank – enfermedad de degos – Spanish English Dictionary

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. Go to the members area of the website of the AEDV, https: Differential diagnosis The histology of early lesions resembles cutaneous lupus erythematosus see this term. Diagnostic methods Diagnosis is based primarily on the cutaneous clinical picture that is nearly pathognomonic.

  INCORRECT PDEOBJECT TYPE PDF

As all patients may potentially develop the systemic, life-threatening variant, an annual follow-up is mandatory.

enfermedad de degos

Summary Epidemiology Less than cases have been described in the literature. All articles enfermeead subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style. Subscriber If you already have your login data, please click here. More developed lesions show prominent changes in the dermoepidermal junction, with atrophy of the epidermis and an area of sclerosis in the papillary dermis.

SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

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. Previous article Next article.

Enfermedad de Degos

Show more Show less. For all other comments, please send your remarks via contact us. In the year has engermedad indexed in the Medlinedatabase, and has become a vehicle for expressing the most current Spanish medicine and modern. The documents contained in this web site are presented for information purposes only. Continuing navigation will be considered as acceptance of this use.

The etiopathogenesis of the disease remains unknown. Specialised Enfermexad Services Eurordis directory.

enfermedad de Degos – English Translation – Word Magic Spanish-English Dictionary

Over several days, the center of the lesions sinks and develops a characteristic morphology: 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. Idiopathic, monosymptomatic, cutaneous presentations are benign, however, systemic manifestations can develop years after the occurrence of skin lesions.

  BUV24 DATASHEET PDF

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.

Subscribe to our Newsletter. Systemic lesions may affect the gastrointestinal tract and the central nervous system CNS and are potentially lethal. Si continua navegando, consideramos que acepta su uso. MAP onset occurs in adults aged with skin lesions that appear initially as small erythematous papules, predominantly on the trunk and the upper extremities.

Additional information Further information on this disease Classification s 3 Gene s 0 Clinical signs and symptoms Publications in PubMed Other website s 7. Etiology The etiopathogenesis of the disease remains unknown.

This condition is chronic and lesions persist over years, often throughout life.

Systemic manifestations are progressive and may lead to serious complications: If you are a member of the AEDV: Many patients have been reported to have defects in blood coagulation. The material is ee no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.

The histology of early lesions resembles cutaneous lupus erythematosus see this term. Later a wedge-shaped connective tissue necrosis in the deep dermis, due to a thrombotic occlusion of the small arteries degoa sparse lymphocytes, occurs.