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Published on: October 11, 2024
Persistent Conductive Hearing Loss After Tympanostomy Tube Placement Due to High-Riding Jugular Bulb
Douglas J Totten1, Nauman F Manzoor2, Joseph Aulino3
1Vanderbilt University School of Medicine, Nashville, TN, U.S.A.
Insights
High-riding jugular bulb (HRJB) is a rare condition causing conductive hearing loss. This case highlights HRJB
Area of Science:
- Otolaryngology
- Radiology
- Medical Case Reports
Background:
- High-riding jugular bulb (HRJB) is an uncommon anatomical variation.
- It is typically asymptomatic but can present with various auditory and vestibular symptoms.
- The precise etiology of HRJB is not fully understood, likely involving postnatal developmental factors.
Observation:
- A male adolescent presented with unilateral conductive hearing loss (CHL) after tympanostomy tube placement.
- Computed tomography revealed a high-riding jugular bulb eroding the posterior semicircular canal and obstructing the round window niche.
- The patient reported no vestibular symptoms, only hearing loss.
Findings:
- HRJB can cause CHL through mechanisms like third-window defects or middle ear obstruction.
- While sensorineural hearing loss, tinnitus, and vertigo are known complications, CHL is less common.
- Imaging is crucial for diagnosing rare causes of CHL, including HRJB.
Implications:
- Recognizing HRJB as a rare cause of CHL is vital for accurate diagnosis and patient counseling.
- Management requires careful consideration of individual anatomy and potential treatment benefits.
- Further research into HRJB's pathogenesis and management strategies is warranted.
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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