Author/Authors :
GHAFFARI JAVAD نويسنده , Ghasemi Maryam نويسنده Department of Pathology, School of Medicine, Mazandaran University of Medical Sciences, Sari, IR Iran , Gohardehi Farzad نويسنده Department of primary health care, School of Medicine, mazandaran University of Medical Science, sari, Iran. , Abedian- Kenari Saeed نويسنده
Abstract :
Background: Hyper IgE syndrome (HIES) is a rare primary immune deficiency, described as Job`s syndrome characterized by increased serum levels of IgE, eczema, recurrent cutaneous and pulmonary infections. In this paper, we presented a case of Hyper IgE syndrome.Case Presentation: A 16-year-old Iranian boy presented with a one year history of skin lesions in knees and elbows was diagnosed of psoriasis disease. He had a history of recurrent infections including otitis media, pneumonia, diarrea and skin infection. Laboratory results showed increased level of total IgE and normal in other immunoglobulin. Histologic finding showed hyperkeratosis, parakeratosis of acanthotic epidermis with regular elongation of rete ridges diagnose psoriasis disorder.Conclusion: In conclusion, this is the first case of hyper IgE patient with psoriasis disorder. We addressed the important laboratory findings and actual theories explaining possible association between hyper IgE immunoglobulinemia and psoriasis disorder.
