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[Eosinophilic fasciitis and aplastic anemia]. / Fasceíte eosinofílica e aplasia medular.
Falcão, Sandra; Mourão, Ana F; Ribeiro, Célia; Pinto, Teresa L; Mateus, Margarida; Araújo, Paula; Nero, Patrícia; Pimentão, J Bravo; Branco, J Cunha.
Afiliación
  • Falcão S; Serviço de Reumatologia, Centro Hospitalar de Lisboa Ocidental, EPE, Hospital Egas Moniz, Lisboa. sfalcao76@gmail.com
Acta Reumatol Port ; 34(1): 120-6, 2009.
Article en Pt | MEDLINE | ID: mdl-19365308
Eosinophilic fasciitis is a rare rheumatic condition characterized by inflammatory thickening of the skin and fascia, peripheral eosinophilia, elevated erythrocyte sedimentation rate and hypergammaglobulinemia. Internal organ involvement is uncommon. It is often difficult to diagnose eosinophilic fasciitis and its course may be variable. Glucocorticoids are most commonly used in the treatment but in many cases they are ineffective, requiring combined immunosuppressive treatment. Several cases of eosinophilic fasciitis and serious haematological disorders such as immune thrombocytopenia, Hodgkin's disease and aplastic anaemia have been described. The authors report an atypical severe case of eosinophilic fasciitis complicated by aplastic anaemia non responsive to treatment.
Asunto(s)
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Base de datos: MEDLINE Asunto principal: Eosinofilia / Fascitis / Anemia Aplásica Idioma: Pt Revista: Acta Reumatol Port Año: 2009 Tipo del documento: Article
Buscar en Google
Base de datos: MEDLINE Asunto principal: Eosinofilia / Fascitis / Anemia Aplásica Idioma: Pt Revista: Acta Reumatol Port Año: 2009 Tipo del documento: Article