Cochlear implantation in a 10-year old boy with Pendred syndrome and extremely enlarged endolymphatic sacs

Cochlear Implants Int. 2019 Mar;20(2):100-103. doi: 10.1080/14670100.2018.1550849. Epub 2018 Nov 28.

Abstract

A 10-year-old boy with fluctuating sensorineural hearing loss (SNHL) and biallelic mutations in the SLC26A4 gene and with inner ear anomalies received a cochlear implantation. SLC26A4 mutations are associated with variable degrees of SNHL and enlarged vestibular aqueducts (EVA), identified either as non-syndromic EVA or classic Pendred syndrome; the latter also associated with thyroid dysfunction. The inner ear malformations in this group of patients have been considered a relative contraindication against cochlear implantation because of the potential per- and postoperative complications such as peroperative cerebrospinal fluid leak or postoperative vestibular symptoms. In the current case there were no surgical or postoperative complications, indicating that extremely enlarged endolymphatic sacs are not as such a contraindication for cochlear implantation. This case also illustrates the management dilemma of an appropriate timing for cochlear implantation.

Keywords: Cochlear implantation; Enlarged endolymphatic sacs; Enlarged vestibular aqueduct; Pendred syndrome; SLC26A4; Temporal bone.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Cochlear Implantation / adverse effects*
  • Contraindications, Procedure
  • Endolymphatic Sac / pathology
  • Endolymphatic Sac / surgery*
  • Goiter, Nodular / genetics
  • Goiter, Nodular / pathology
  • Goiter, Nodular / surgery*
  • Hearing Loss, Sensorineural / genetics
  • Hearing Loss, Sensorineural / pathology
  • Hearing Loss, Sensorineural / surgery*
  • Humans
  • Male
  • Mutation
  • Serotonin Plasma Membrane Transport Proteins / genetics
  • Vestibular Aqueduct / abnormalities*
  • Vestibular Aqueduct / pathology
  • Vestibular Aqueduct / surgery

Substances

  • SLC6A4 protein, human
  • Serotonin Plasma Membrane Transport Proteins

Supplementary concepts

  • Deafness, Autosomal Recessive 4
  • Pendred syndrome