Internal auditory canal meningocele-perilabyrinthine/translabyrinthine fistula: Case report and imaging

Authors

  • Carl M. Truesdale MD,

    1. Department of Otolaryngology, University of Michigan, Ann Arbor, Michigan
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  • Ryan B. Peterson MD,

    1. Department of Radiology and Imaging Sciences, Emory University School of Medicine, Atlanta, Georgia, U.S.A.
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  • Patricia A. Hudgins MD,

    1. Department of Radiology and Imaging Sciences, Emory University School of Medicine, Atlanta, Georgia, U.S.A.
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  • Esther X. Vivas MD

    Corresponding author
    1. Department of Otolaryngology, Emory University School of Medicine, Atlanta, Georgia, U.S.A.
    • Send correspondence to Esther X. Vivas, MD, Emory School of Medicine, Department of Otolaryngology, Emory University Hospital Midtown, 550 Peachtree St., 9th Fl 4400, Atlanta, GA 30322. E-mail: evivas@emory.edu

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  • The authors have no funding, financial relationships, or conflicts of interest to disclose.

Abstract

The case of a 17-year-old patient with progressive unilateral sensorineural hearing loss and temporal bone malformations concerning for internal auditory canal meningocele with translabyrinthine/perilabyrinthine cerebrospinal fluid fistula is presented with associated computed tomography and magnetic resonance imaging. As the second reported case of an unruptured internal auditory canal meningocele with translabyrinthine/perilabyrinthine fistula, the case presents several clinically relevant points for otologists, neurotologists, and neuroradiologists. Although rare, it is an additional entity to consider as a cause of unilateral sensorineural hearing loss and may pose a risk for developing meningitis and possible “gushing” of cerebrospinal fluid should surgical intervention be attempted. Laryngoscope, 126:1931–1934, 2016

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