Cryptococcal Meningoencephalitis in a Patient with Hyper IgM Syndrome Due to CD40 Deficiency: Case Report and Literature Review
Maram Al-Banyan1, Abdulhadi Alqahtani1, Farrukh Sheikh1, Agha M. Rehan Khaliq2, Hasan Al Rayes1, Ashraf Al-Tarifi1, Bandar Al-Saud1 & Rand K. Arnaout2 Show affiliations
- King Faisal Specialist Hospital and Research Centre, Saudi Arabia
- Alfaisal University, Saudi Arabia
American Journal of Infectious Diseases, Volume 15, Issue 1, pp. 24–28 · doi.org/10.3844/ajidsp.2019.24.28
Abstract
Hyper-IgM syndrome (HIGM) due to CD40 deficiency is a very rare form of combined immunodeficiency with increased susceptibility to opportunistic infections. Cryptococcus is an opportunistic infection usually affecting immunocompromised individuals. This is the first report to describe a patient with HIGM due to CD40 deficiency presenting with meningoencephalitis secondary to Cryptococcus infection.
Licence and reuse
Open access. This article is licensed under a Creative Commons Attribution 3.0 Licence (CC BY 3.0), as printed on the article, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original authors and the source. No permission is needed.
How to reuse this articleResponses (0)
About this article
Al-Banyan, M., Alqahtani, A., Sheikh, F., Khaliq, A. M. R., Al Rayes, H., Al-Tarifi, A., Al-Saud, B. & Arnaout, R. K. (2019). Cryptococcal Meningoencephalitis in a Patient with Hyper IgM Syndrome Due to CD40 Deficiency: Case Report and Literature Review. American Journal of Infectious Diseases, 15(1), 24–28. https://doi.org/10.3844/ajidsp.2019.24.28
- Licence
- CC BY 3.0
- Issue
- Volume 15, Issue 1
- Policies
- Editorial independenceUse of generative AIData availabilityAppeals and complaints
- Version
- Version of record
