Hyperimmunoglobulin E-recurrent infection syndrome in a patient with juvenile dermatomyositis
The Korean Journal of Internal Medicine
;
: 95-98, 1999.
Article
Dans Anglais
| WPRIM
| ID: wpr-125505
ABSTRACT
A 13-year-old girl presented with multiple skin abscesses. She was diagnosed as having juvenile dermatomyositis (DM) at the age of 7 years. She had suffered from recurrent skin infections, atypical pruritic dermatitis and pneumonia since the age of 8 years. Bacteriologic and fungal cultures for skin abscesses and oral mucosa were positive S. aureus and C. albicans, respectively. Chemotactic defect in peripheral blood neutrophils was observed. The level of serum IgE was markedly elevated, and anti-S.aureus specific IgE was found. A diagnosis of hyperimmunoglobulin E-recurrent infection syndrome (HIE) was made and she was successfully treated with surgical drainage and antibiotics. To our knowledge, this is the first case report of HIE in a patient with juvenile dermatomyositis.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Infections à staphylocoques
/
Staphylococcus aureus
/
Immunoglobuline E
/
Adolescent
/
Dermatomyosite
/
Syndrome de Job
Limites du sujet:
Femelle
/
Humains
langue:
Anglais
Texte intégral:
The Korean Journal of Internal Medicine
Année:
1999
Type:
Article
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