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Abstract

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.

Keywords

Hyper IgE syndrome tumours lymphoid

Article Details

How to Cite
I B, E., S A, B., & D, M. (2000). Development of Non-Hodgkin’s Lymphoma in a Child with Hyper-Ige Syndrome. Sultan Qaboos University Medical Journal, 2(1), 65–67. Retrieved from https://journals.squ.edu.om/index.php/squmj/article/view/1197