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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Later a wedge-shaped connective tissue necrosis in the deep dermis, due to a thrombotic occlusion of the small arteries and sparse lymphocytes, occurs. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.
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.
Face, scalp, palms of hands and soles of feet are rarely involved. As all patients may potentially develop the systemic, life-threatening variant, an annual follow-up is mandatory. 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.
Diagnostic methods Diagnosis is based primarily on the cutaneous clinical picture that is nearly pathognomonic. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and deos measure of the journal’s impact.
The etiopathogenesis of the disease remains unknown. Go to the members area of the website of the AEDV, https: Additional information Further information on this disease Classification s 3 Gene s 0 Clinical signs and symptoms Publications in PubMed Other website s 7.
Prognosis Idiopathic, monosymptomatic, cutaneous presentations are benign, however, systemic manifestations can develop years after the occurrence of skin lesions. If you are a member of the AEDV: Genetic counseling A genetic predisposition with an autosomal dominant trait has been suggested. Hypotheses implicating vasculitis, coagulopathy or a primary dysfunction of endothelial cells have been proposed. Subscriber If you already have your login data, please click here.
The documents contained in this web site are presented for information purposes only. MAP onset occurs in adults aged with skin lesions that appear initially as small erythematous papules, predominantly on the trunk and the upper extremities.
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Systemic lesions may affect the gastrointestinal enfermead and the central nervous system CNS and are potentially lethal. 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. Etiology The etiopathogenesis of the disease remains unknown. Check this box if you wish to receive a copy of your message.
More developed lesions show prominent changes in the dermoepidermal junction, with atrophy of the epidermis and an area of sclerosis in the papillary dermis. Only comments written in English can be processed. Read this article in English. Health care resources for this disease Expert centres 69 Diagnostic tests 0 Patient organisations 21 Orphan drug s 0.
Previous article Next article. More developed lesions can imitate lichen sclerosus see this term. From Monday to Friday from 9 a.
This item has received. Print Send to a friend Export reference Mendeley Statistics. In the year has been indexed in the Medlinedatabase, and has become a vehicle for expressing the most current Spanish medicine and modern.
This condition is chronic and lesions persist over years, often throughout life. Systemic manifestations are progressive and may lead to serious enfermedadd