Iranian Journal of Allergy, Asthma and Immunology (Apr 2019)

A Rare Case of Hyper IgE Syndrome with Vocal Cords Involvement

  • Samin Sharafian,
  • Masoud Movahedi,
  • Arash Kalantari,
  • Nima Parvaneh,
  • Mohammad Gharagozlou

DOI
https://doi.org/10.18502/ijaai.v18i2.926
Journal volume & issue
Vol. 18, no. 2

Abstract

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Hyperimmunoglobulin E syndrome (HIGE) is considered as a phagocytic or a newly classified complex and heterogeneous primary immunodeficiency disease with symptoms such as increased levels of immunoglobulin E, eczema, and, recurrent lung and skin infections. In this paper, we have presented a rare case of this syndrome. A 9-year-old Iranian girl presented with a history of pruritic maculopapular rash who was eventually diagnosed as a case of HIGE. In her recent admission, she had dysphonia, stridor and huge cauliflower cutaneous lesions on her neck, finger and vocal cords, which did not respond to intravenous antibiotics, and ultimately required surgical removal.

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