Abstract
Recurrent pneumonia with cavitation leading to pneumatoceles, secondary fungal infections, and hemoptysis are major causes of mortality and morbidity in patients with hyper-IgE syndrome. Prevention and aggressive treatment of pneumonia in these patients are essential to prevent further lung damage, but treatment may be delayed because the classic signs/symptoms of infection such as fever, chills, or rigors may be lacking. Early imaging to identify infection is essential for diagnosis and treatment. The mainstay of therapy is continuous, full-dose daily trimethoprim-sulfamethoxazole and commonly fungal coverage. Because hyper-IgE syndrome is a progressive disease, patients' condition may worsen despite compliance with prophylactic therapy.
Original language | English |
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Pages (from-to) | 1054-1058 |
Number of pages | 5 |
Journal | Journal of Allergy and Clinical Immunology: In Practice |
Volume | 4 |
Issue number | 6 |
DOIs | |
State | Published - 1 Nov 2016 |
Keywords
- Aspergilloma
- Eczema
- Immunodeficiency
- STAT3
- hyper-IgE syndrome