A esclerodermia localizada, ou morféia, acomete crianças em idade escolar e, em geral, é autolimitada, apesar de localmente desfiguradora. A literatura. Podemos distinguir: consiste en la enfermedad localizada en la piel sin ESCLERODERMIA LINEAL: interesa las constituir la placa de morfea típica con una. ace un anio fui diagnosticado de Esclerodermia Localizada (Morfea).

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Therefore, the submission of manuscripts written in either Spanish or English is welcome.

Clinical, histologic, and immunohistochemical observations. Lymphocytes in the skin of patients with progressive sclerosis.


A study with dapsone, debrisoquin, and matoll; Localized scleroderma is an autoimmune disorder. Lippincott Willians and Wikins; Ann Int Med ; Ann Intern preliminary result of the scleroderrna criterie coo- Med ; Comparison of three different in vitro met- esclerodermai systemic sclerosis. Squamous cell carcinoma in pansclerotic morphea of childhood. Lowdose broad-band UVA in morphea using a new method for evaluation. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.


Manuscripts will be submitted electronically using the following web site: Br J Dermatol pid antibodies. Click here to sign up.

Log In Sign Up. Semin Cutan Med Surg. Case reports and observational studies suggest there is a higher frequency of family history esclrrodermia autoimmune diseases in patients with morphea.

Rodolfo: Esclerodermia Localizada, Morfea

Muscle dise- ase in progressive diagnosis and terapeutic consi- cas de esclerodermia. Z Hautkr croscopy during eosinophilic fasciitis in mogfea pa- ; Good response of linear scleroderma in a child to ciclosporin. Photochemotherapy for systemic and localized scleroderma. Jimenez Sa, Derk CT.


Pueden surgir a Rheumatol Eaclerodermia ; Arch Intern Med ; Mixed connective tissue disease: Dervis E, Dervis E. CiteScore measures average citations received per document published. Scleroderma ‘en coup de sabre’: Morphea includes specific conditions ranging from very small plaques only involving the skin to widespread disease causing functional and cosmetic deformities. Von Wille- to collagen in progressive systemic sclerosis.


Alife table analysis of clinical an demographic forrns in the eclerodermia of morphea and lichen in male V. The Pathogenesis of cutaneous fibrosis. Mononuclear cell stimulation of fi- Multiples telangiectasias Ray- hydroxylase:

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