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Bol. Asoc. Méd. P. R ; 92(4/8): 59-62, Apr.-Aug. 2000.
Artigo em Inglês | LILACS | ID: lil-411272

RESUMO

The hypereosinophilic syndrome (HES) is a heterogeneous disease characterized by sustained eosinophilia for a period of at least six months with evidence of organ involvement. Its manifestations range from a benign disorder not requiring any therapy to an aggressive, malignant variety refractory to common treatments. Diverse therapies have been used, including steroids, hydroxyurea, and chemotherapy, with variable responses. Recently alpha-interferon therapy has been shown effective in this disorder. Of the various prognostic factors, elevated serum immunoglobulin E (IgE) levels is considered among the most favorable, with most patients presenting with a [quot ]benign[quot ] disorder, not requiring therapy. We describe a patient presenting with an aggressive variant of HES despite having elevated IgE levels. The patient had a dramatic and lasting response to alpha-interferon


Assuntos
Humanos , Masculino , Adulto , Antineoplásicos/uso terapêutico , Interferon-alfa , Síndrome Hipereosinofílica/tratamento farmacológico , Imunoglobulina E/sangue , Resistência a Medicamentos , Síndrome Hipereosinofílica/sangue , Síndrome Hipereosinofílica/diagnóstico
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