Volume 131, Issue 4 pp. E1272-E1274
Case Report

Persistent Conductive Hearing Loss After Tympanostomy Tube Placement Due to High-Riding Jugular Bulb

Douglas J. Totten BA

Douglas J. Totten BA

Vanderbilt University School of Medicine, Nashville, TN, U.S.A.

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Nauman F. Manzoor MD

Nauman F. Manzoor MD

Department of Otolaryngology, Vanderbilt University Medical Center, Nashville, TN, U.S.A.

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Joseph Aulino MD, MMHC

Joseph Aulino MD, MMHC

Department of Radiology, Vanderbilt University Medical Center, Nashville, TN, U.S.A.

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Pooja Santapuram BS

Pooja Santapuram BS

Vanderbilt University School of Medicine, Nashville, TN, U.S.A.

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Alejandro Rivas MD

Corresponding Author

Alejandro Rivas MD

Department of Otolaryngology, Vanderbilt University Medical Center, Nashville, TN, U.S.A.

Send correspondence to Alejandro Rivas, MD, Department of Otolaryngology-Head and Neck Surgery, The Bill Wilkerson Center for Otolaryngology & Communication Sciences, 7209 Medical Center East South Tower, 1215 21st Avenue South, Nashville, TN 37232-8605. E-mail: [email protected]

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First published: 29 January 2021
Citations: 3

A.R. is consultant for Med-El, Advanced Bionics, Cochlear, Grace Medical, Stryker, and Cook Medical. The authors have no other funding, financial relationships, or conflicts of interest to disclose.

Editor's Note: This Manuscript was accepted for publication on June 16,,2020.

Abstract

High-riding jugular bulb (HRJB) is a rare condition not often observed in the clinical setting that occurs in 1% to 3% of cases. The jugular bulb is not present at birth, and the precise size and location likely depends on a myriad of postnatal events. This report describes the case of a male adolescent who experienced persistent conductive hearing loss (CHL) unilaterally following bilateral tympanostomy tube placement. Subsequent workup included computed tomography, which identified a very high jugular bulb eroding the posterior semicircular canal and occluding the round window niche. The patient had no hearing or vestibular symptoms aside from CHL and continues to be observed on a regular basis. HRJB is a rare disorder that has been known to erode the posterior semicircular canal, resulting in possible tinnitus, vertigo, dizziness, and/or sensorineural hearing loss. CHL has been reported in HRJB cases, although it is uncommon. HRJB may result in CHL through a third-window defect shunting hydromechanical energy away from the round window or due to middle ear blockage. Imaging is useful in ascertaining rare causes of CHL, such as HRJB. Because HRJB is not easily fixable, it is important to recognize it as a rare cause of CHL for appropriate patient counseling. Possible interventions should be tailored to the patient after careful consideration of contralateral anatomy and likely benefits. Laryngoscope, 131:E1272–E1274, 2021

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