RESUMO

We describe 8 children with hyper-IgE syndrome who had papulopustular eruption on the face and scalp in the first year of life. Seven of the 8 patients had persistent peripheral eosinophilia and 3 had leukocytosis noted before diagnosis. Skin biopsy specimens in 6 patients revealed spongiosis and perivascular dermatitis and/or folliculitis with a predominance of eosinophils. Two patients had bone fractures and osteopenia. Recurrent pneumonia occurred in 6 children and pneumatoceles in 5. The diagnosis of hyper-IgE syndrome was made an average of 18 months after the onset of the initial papulopustular eruption. These findings may lead to earlier recognition of the disease and institution of appropriate treatment.

Assuntos

Eczema/etiologia , Síndrome de Job/complicações , Antibacterianos/uso terapêutico , Biópsia , Diagnóstico Diferencial , Eczema/diagnóstico , Eczema/tratamento farmacológico , Feminino , Humanos , Imunoglobulina E/sangue , Lactente , Bem-Estar do Lactente , Recém-Nascido , Síndrome de Job/diagnóstico , Síndrome de Job/tratamento farmacológico , Masculino , Recidiva , Pele/patologia , gama-Globulinas/uso terapêutico