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Published on: February 21, 2018
Cochlear Meniere's: A Distinct Clinical Entity With Isolated Cochlear Hydrops on High-Resolution MRI?
Jose E Alonso1, Gail P Ishiyama2, Rance J T Fujiwara1
1Department of Head and Neck Surgery, University of California, Los Angeles, Los Angeles, CA, United States.
Insights
Isolated cochlear endolymphatic hydrops (EH) primarily causes auditory symptoms like hearing loss and tinnitus, not vertigo. This condition, common in older males, differs from Meniere's disease.
Area of Science:
- Otolaryngology
- Neuroscience
- Radiology
Background:
- Endolymphatic hydrops (EH) is a condition affecting the inner ear.
- Isolated cochlear EH is a less understood variant.
- Differentiating EH variants is crucial for diagnosis and management.
Purpose of the Study:
- To describe the clinical and audiological characteristics of patients with isolated cochlear EH.
- To distinguish isolated cochlear EH from Meniere's disease and other EH variants.
- To identify potential treatment responses and comorbidities.
Main Methods:
- A clinical case series design was employed.
- High-resolution delayed-intravenous contrast MRI was used to identify isolated cochlear EH.
- Audiometric and vestibular testing, along with clinical history, were analyzed.
Main Results:
- Ten patients with isolated cochlear EH were identified, none meeting Meniere's disease criteria.
- Predominant symptoms included unilateral aural fullness (70%), tinnitus (80%), and hearing loss (90%).
- Vertigo was infrequent (10%), and hearing loss was significantly worse in affected ears (37.8 dB PTA vs. 17.9 dB). Acetazolamide showed 86% subjective improvement.
Conclusions:
- Isolated cochlear EH presents mainly with auditory symptoms and minimal vertigo, distinguishing it from Meniere's disease.
- This condition is more prevalent in males in their mid-60s with low migraine comorbidity.
- Cochlear Meniere's disease may represent a distinct clinical entity or variant of Meniere's disease.
Abstract:
Objective: Describe the clinical characteristics of patients with isolated cochlear endolymphatic hydrops (EH). Study design: Clinical case series. Setting: Tertiary Neurotology referral clinic. Patients: All subjects presenting to a University Neurotology clinic during a 1-year period from July 2015 until August 2016 who had isolated cochlear EH on MRI. Patients with a history of temporal bone surgery prior to the MRI were excluded. Intervention: High-resolution delayed-intravenous contrast MRI. Main outcome measures: Audiometric and vestibular testing, clinical history analysis. Results: 10 subjects demonstrated isolated, unilateral cochlear hydrops on MRI. None of these patients met the criteria for Meniere's disease. Mean age of the group was 66.4 years and most were males (70%). Unilateral aural fullness (70%), tinnitus (80%), and hearing loss (90%) were frequently observed. Only one patient presented with unsteadiness (10%) and one patient had a single isolated spell of positional vertigo 1 month prior to the MRI (10%) but no further vertigo spells in the 4 years following the MRI. The mean PTA was 37.8 dB which was significantly decreased from the non-affected ear with PTA of 17.9 (p < 0.001). One patient developed vertiginous spells and unsteadiness 4 years after initial presentation and a repeat MRI revealed progression to utricular, saccular and cochlear hydrops. Vestibular testing was obtained in five patients with one patient presenting with 50% caloric paresis and all others normal. The most common treatment tried was acetazolamide in seven patients with 86% reporting subjective clinical improvement. Two out of the 10 patients had a history of migraine (20%). Conclusions: Patients with MRI exhibiting isolated cochlear EH present with predominantly auditory symptoms: mild to moderate low-frequency hearing loss, aural fullness, tinnitus without significant vertigo. Isolated cochlear hydrops is more common in males, average age in mid-60's and there is a low comorbidity of migraine headaches. This contrasts significantly with patients with isolated saccular hydrops on MRI from our prior studies. We believe that isolated cochlear EH with hearing loss but no vertigo is distinct from Meniere's disease or its variant delayed endolymphatic hydrops. We propose that cochlear Meniere's disease represents a distinct clinical entity that could be a variant of Meniere's disease.
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