Definite Vestibular Paroxysmia Comorbid With Definite Ménière’s Disease: A Rare Case Highlighting Diagnostic and Therapeutic Implications
Kento Koda, Makoto Kinoshita, Kentaro Ichijo, Naoko Ogata, Mineko Oka, Kenji Kondo, Chisato Fujimoto

TL;DR
A rare case shows a patient with both Ménière’s disease and vestibular paroxysmia, highlighting the importance of distinguishing these conditions for proper treatment.
Contribution
This paper presents a rare comorbid case of MD and VP, emphasizing diagnostic and therapeutic insights.
Findings
The patient's MD was confirmed by MRI showing endolymphatic hydrops.
VP was diagnosed based on brief vertigo attacks responsive to carbamazepine.
The case highlights the need to differentiate MD and VP for effective treatment.
Abstract
Ménière’s disease (MD) is characterized by episodic vertigo lasting 20 minutes to several hours with fluctuating sensorineural hearing loss. Vestibular paroxysmia (VP) involves brief, recurrent vertigo attacks that typically last less than one minute and are often responsive to carbamazepine. While both diseases can present with accompanying auditory symptoms during vertigo attacks, they differ in attack duration and drug responsiveness. Here, we report a case of definite MD that was subsequently complicated by definite VP. A 46-year-old man presented with fluctuating right-sided sensorineural hearing loss and recurrent vertigo episodes lasting about one hour, consistent with definite MD. Gadolinium-enhanced MRI demonstrated significant endolymphatic hydrops in the right vestibule without neurovascular compression. Initial treatment with isosorbide improved vertigo. One year later, he…
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Taxonomy
TopicsVestibular and auditory disorders · Ophthalmology and Eye Disorders · Cerebral Venous Sinus Thrombosis
