الملخص
This paper reports development of non-Hodgkin’s lymphoma in a 7'/2-year-old patient with hyper IgE syndrome. This rare primary immunodeficiency syndrome is characterized by markedly elevated serum IgE levels, chronic atypical dermatitis and serious recurrent infections. Laboratory features include exceptionally high levels of IgE, near normal levels of IgG, IgA, IgM, with pronounced eosinophilia.
بيانات النشر
- المعرّف الرقمي
- 10.18295/2075-0528.2150
- المجلة
- مجلة جامعة السلطان قابوس الطبية, 2(1), 65-67
- الناشر
- جامعة السلطان قابوس
- وصول مفتوح
- وصول مفتوح ذهبي
- الترخيص
- CC BY-ND 4.0
اقتبس هذه المقالة
APA 7
B, E. I., A, B. S., & Muirhead (2025). Development of Non-Hodgkin's Lymphoma in a Child with Hyper-Ige Syndrome. Sultan Qaboos University Medical Journal, 2(1), 65-67. https://doi.org/10.18295/2075-0528.2150
MLA 9
B, Elnour I., et al. "Development of Non-Hodgkin's Lymphoma in a Child with Hyper-Ige Syndrome." Sultan Qaboos University Medical Journal, vol. 2, no. 1, 2025, pp. 65-67. https://doi.org/10.18295/2075-0528.2150.
شيكاغو (المؤلف–التاريخ)
B, Elnour I., Bamanikar S. A, and Muirhead. 2025. "Development of Non-Hodgkin's Lymphoma in a Child with Hyper-Ige Syndrome." Sultan Qaboos University Medical Journal 2 (1): 65-67. https://doi.org/10.18295/2075-0528.2150.
هارفارد
B, E. I., A, B. S. and Muirhead (2025) 'Development of Non-Hodgkin's Lymphoma in a Child with Hyper-Ige Syndrome', Sultan Qaboos University Medical Journal, 2(1), pp. 65-67. doi:10.18295/2075-0528.2150.
فانكوفر
B EI, A BS, Muirhead. Development of Non-Hodgkin's Lymphoma in a Child with Hyper-Ige Syndrome. Sultan Qaboos University Medical Journal. 2025;2(1):65-67. doi:10.18295/2075-0528.2150
IEEE
E. I. B, B. S. A, and Muirhead, "Development of Non-Hodgkin's Lymphoma in a Child with Hyper-Ige Syndrome," Sultan Qaboos University Medical Journal, vol. 2, no. 1, pp. 65-67, 2025, doi: 10.18295/2075-0528.2150.