Cryptococcal meningitis in a child with hyperimmunoglobulin E syndrome

B. ‐Z Garty, B. Wolacfr, S. Ashkenazi, Y. Weisman, A. Rachmel, M. Nitzan

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

A 13‐year‐old boy with hyperimmunoglobulin E (hyper‐IgE) syndrome presented with headache, blurred vision, photophtobia and bilateral papilledema due to cryptococcal meningitis. Treatment with amphotericin B, and S‐fluorocytosine for several weeks and repeated lumbar punctures did not reduce the intracranial pressure, and a myeloperitoneal shunt was performed. The child was maintained on fluconazole for an additional six months. Patients with hyper‐IgE syndrome are at increased risk of opportunistic fungal infections such as cryptococcal meningitis.

Original languageEnglish
Pages (from-to)175-177
Number of pages3
JournalPediatric Allergy and Immunology
Volume6
Issue number3
DOIs
StatePublished - Aug 1995
Externally publishedYes

Keywords

  • cryptococcal meningitis
  • hyperimmunoglobulin E syndrome

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