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Endolymphatic hydrops mimicking obstructive Eustachian tube dysfunction: preliminary experience and literature review
Endolymphatic hydrops mimicking obstructive Eustachian tube dysfunction: preliminary experience and literature review
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Endolymphatic hydrops mimicking obstructive Eustachian tube dysfunction: preliminary experience and literature review
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Endolymphatic hydrops mimicking obstructive Eustachian tube dysfunction: preliminary experience and literature review
Endolymphatic hydrops mimicking obstructive Eustachian tube dysfunction: preliminary experience and literature review

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Endolymphatic hydrops mimicking obstructive Eustachian tube dysfunction: preliminary experience and literature review
Endolymphatic hydrops mimicking obstructive Eustachian tube dysfunction: preliminary experience and literature review
Journal Article

Endolymphatic hydrops mimicking obstructive Eustachian tube dysfunction: preliminary experience and literature review

2021
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Overview
Purpose Aural fullness is a common symptom of middle ear diseases, most importantly Eustachian tube dysfunction (ETD). Yet, aural fullness may also be caused by inner ear disorders, such as hydropic ear diseases. Here, we report our experience with endolymphatic hydrops (EH) mimicking ETD. Furthermore, we review the literature related to (i) EH as a differential diagnosis of symptoms suggesting ETD and (ii) the pathophysiology and treatment of aural fullness due to inner ear disorders. Methods We retrospectively included adult patients with aural fullness as chief complaint and radiographically diagnosed EH. Hearing and Eustachian tube function were assessed using audiometry, tympanometry, and tubomanometry. Primarily suspected ETD was treated by balloon dilatation of the Eustachian tube (BDET). The endolymphatic space of the inner ear was imaged using gadolinium-enhanced MRI (Gd-MRI) including a 3D-real inversion-recovery sequence after intravenous gadolinium administration. Results We report three affected ears of two patients (two females, age 42 and age 51) with aural fullness as chief complaint. Audiometry of main speech frequencies was normal in all affected ears. In one ear, there was a type A tympanogram and in two ears, there was a type B tympanogram. In both patients, medical treatment for ETD and BDET were unsuccessful. Gd-MRI of the inner ears revealed cochlear EH in 3/3 ears affected by aural fullness, but not in the unaffected ear. Conclusion EH may underlay cases with aural fullness and could in these cases explain unsuccessful treatment for ETD. As ETD is often treated by invasive procedures, distinguishing ETD from EH as the underlying cause of aural fullness is important. Our findings raise the question whether Gd-MRI to rule out EH is indicated in patients with unexplained aural fullness, in particular after unsuccessful interventional treatment for ETD.