Relato de Caso

Eosinophilic fasciitis

Publicado em: 2016

Autores

  • Elisa Baranski Lamback
    Hospital Federal da Lagoa - Rio de Janeiro (RJ), Brazil.
  • Fernanda Simões Seabra Resende
    Hospital Regional da Asa Norte (HRAN) - Brasília (DF), Brazil.
  • Thiara Cristina Rocha Lenzi
    Escola Superior de Ciências da Saúde (ESCS) - Brasília (DF), Brazil.

Resumo

Eosinophilic fasciitis is a rare sclerodermiform syndrome of unknown etiology. It is characterized by the thickening of the muscular fascia and subcutaneous tissue, with a variable infiltration of eosinophils. Peripheral eosinophilia, poly or monoclonal hypergammaglobulinemia and increased erythrocyte sedimentation rate can be seen. Clinical features begin acutely, with local edema and a painful and symmetrical stiffening of the limbs, progressing rapidly to fibrosis, which can limit joint movements. Some cases have a history of strenuous physical exercise or trauma. The diagnosis is confirmed by a deep skin biopsy. Glucocorticoids in high doses is the treatment of choice. We report a typical eosinophilic fasciitis case with peripheral eosinophilia and dramatic response to pulse therapy with methylprednisolone.

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