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Common variable immunodeficiency syndrome: a difficult diagnostic problem

Published online by Cambridge University Press:  01 August 2007

C Spyridakou*
Affiliation:
Department of Otolaryngology and Head and Neck Surgery, Singleton Hospital, Swansea, UK
S Berry
Affiliation:
Department of Otolaryngology and Head and Neck Surgery, Singleton Hospital, Swansea, UK
J Phillipps
Affiliation:
Department of Otolaryngology and Head and Neck Surgery, Singleton Hospital, Swansea, UK
*
Address for correspondence: Dr C Spyridakou, Department of Audiological Medicine, St Ann's Hospital, St Ann's Road, London, N15 3TH, UK. E-mail: [email protected]

Abstract

Objective:

We present a rare case of an adult male with undiagnosed common variable immunodeficiency syndrome who presented to the ENT department with refractory chronic sinusitis and otitis media with effusion.

Method:

Case report and a review of the international literature concerning common variable immunodeficiency syndrome in adults and upper respiratory tract involvement.

Results:

A 37-year-old male presented to the ENT department with refractory chronic sinusitis and otitis media with effusion. The diagnosis of common variable immunodeficiency syndrome was delayed, and difficult, primarily due to minimal symptoms with no lower respiratory tract involvement and negative past or family medical history.

Conclusion:

Early diagnosis helps to prevent morbidity and even mortality. This article highlights how difficult and important it is to make an early diagnosis of common variable immunodeficiency syndrome. Early diagnosis will only be made by increased awareness of this condition.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 2007

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References

1 Report of a WHO sponsored meeting. Primary immunodeficiency diseases. Immunodefic Rev 1989;1:173205Google Scholar
2 Buckley, RH. Humoral immunodeficiency. Clin Immunol Immunopathol 1986;40:1324CrossRefGoogle ScholarPubMed
3 Spickett, GP, Misbah, SA, Chapel, HM. Primary antibody deficiency in adults. Lancet 1991;337:281–4CrossRefGoogle ScholarPubMed
4 Hermaszewski, RA, Webster, AD. Primary hypogammaglobulinaemia: a survey of clinical manifestations and complications. Q J Med 1993;86:3142Google ScholarPubMed
5 Polmar, SH. The role of immunologist in sinus disease. J Allergy Clin Immunol 1992;90:511–14; discussion 514–15CrossRefGoogle ScholarPubMed
6 Ferguson, BJ, Mabry, RL. Laboratory diagnosis. Otolaryngol Head Neck Surg 1997;117:S1226CrossRefGoogle ScholarPubMed
7 Spickett, GP, Chapel, HM. Report on the audit of patients with primary antibody deficiency in the United Kingdom 1993–1996 Newcastle: Newcastle upon Tyne Hospitals NHS Trust, 1998Google Scholar
8 Blore, J, Haeney, MR. Primary antibody deficiency and diagnostic delay. BMJ 1989;298:516–17CrossRefGoogle ScholarPubMed
9 Cooney, TR, Huissoon, AP, Powell, RJ, Jones, NS. Investigation for immunodeficiency in patients with recurrent ENT infections. Clin Otolaryngol Allied Sci 2001;26:184–8CrossRefGoogle ScholarPubMed
10 European Group for Immunodeficiencies. Intravenous gammaglobulin for immunodeficiency: report from the European Group for Immunodeficiencies(EGID). Clin Exp Immunol 1986;65:683–90Google Scholar