Otological findings in pediatric patients with hypogammaglobulinemia

Iran J Allergy Asthma Immunol. 2014 Jun;13(3):166-73.

Abstract

The main clinical presentation of patients with primary antibody deficiency (PAD) incorporates upper respiratory tract infections comprising otitis media, sinusitis and pneumonia. This study was designed to investigate clinical and paraclinical otological complications in major types of PAD. A cross sectional study was conducted on 55 PAD patients with diagnosis of selective IgA deficiency, common variable immunodeficiency (CVID), X-linked agammaglobulinemia (XLA), and hyper IgM syndrome. All patients underwent otological examinations, audiometry, and auditory brain stem response. Otological complications were detected in 54.5% of PAD patients. Conductive hearing loss was the main finding amongst PID patients (73.3%) followed by sensorineural hearing loss which was present in 8 cases. Otitis media with effusion (21.8%), chronic otitis media (27.2%), tympanosclerosis with intact tympanic membrane (5.4%) and auditory neuropathy (3.6%) were most important found complications. CVID and XLA patients with prophylactic usage of antibiotics had lower rate of audiological complications (p=0.04) and otitis media with effusion (p=0.027). As our results showed, asymptomatic otological findings were not rare in PAD patients; therefore, a systematic otological investigation is recommended as an integral part of the management and follow-up of these patients.

MeSH terms

  • Adolescent
  • Adult
  • Agammaglobulinemia / complications
  • Audiometry
  • Child
  • Common Variable Immunodeficiency / complications
  • Cross-Sectional Studies
  • Ear Diseases / etiology*
  • Evoked Potentials, Auditory, Brain Stem
  • Female
  • Genetic Diseases, X-Linked / complications
  • Hearing Loss, Sensorineural / etiology
  • Humans
  • Hyper-IgM Immunodeficiency Syndrome / complications
  • Immunologic Deficiency Syndromes / complications*
  • Male
  • Otitis Media / etiology

Supplementary concepts

  • Bruton type agammaglobulinemia