We here present a 32-month follow-up of a case of Lermoyez syndrome combined with Meniere's disease. The patient was a 49-year-old male, with a stabilized severe hearing loss in the left ear for about 15 years after Meniere's disease. He started to show typical symptoms of Lermoyez syndrome in the right ear about 32 months ago. Audiologic data were obtained and imaging examinations were performed 0, 9, 15, 28, and 32 months after the onset of the Lermoyez syndrome. Pure tone threshold data obtained 5 months before the onset are also reported. The results show that the hearing thresholds, mainly at low frequencies, elevated rapidly during the first months shortly after the onset of the disease and slowly in later months. The glycerol test resulted in a remarkable hearing improvement at the beginning of the disease, but showed no detectable improvements as the disease advanced. Electrocochleogram revealed a -SP/AP value with click stimulus 0.65 at the 9th month and > 1.0 at the 28th month after the onset. Clinical manifestations of this patient fit well with a pathological endolymphatic hydrops.
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http://dx.doi.org/10.3109/00016480903582139 | DOI Listing |
Acta Otolaryngol
July 2020
ENT Institute and Otorhinolaryngology Department, Eye and ENT Hospital, Fudan University of Eye and ENT Hospital, Shanghai, China.
Lermoyez syndrome (LS) is a rare auditory disorder, the details of LS remain unclear. To investigate the grades of endolymphatic hydrops (ELH) and clinical characteristics of clinically diagnosed LS. Nine patients with clinically diagnosed LS were included.
View Article and Find Full Text PDFActa Otolaryngol
November 2018
a Department of Otolaryngology , National Taiwan University Hospital, Taipei , Taiwan.
Objective: This study revisited seven patients with Lermoyez syndrome over the past 25 years using an inner ear test battery to elucidate its mechanism.
Methods: From 1992 to 2017, we have experienced 4096 patients with Meniere's disease (MD) and seven patients (5 males and 2 females, 8 ears) with Lermoyez syndrome. Two of the Lermoyez patients were elderly, aged 71 and 85 years.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
February 2015
Objective: To investigate the effecacy of cochlear implantation (CI) improving hearing of Lermoyez's syndrome, we retrospectively analyzed a case of Lermoyez's syndrome whose left ear was extremely severe sensorineural deafness and right ear was severe sensorineural deafness.
Method: The patient had completed preoperative audiological examination , vestibular function and imaging examination, then was carried out bilateral endolymphatic sac decompression and left side CI. Follow up after the surgery.
Eur Arch Otorhinolaryngol
February 2012
MSA ENT Academy Center, Via Riccardo da S.Germano 41, 03043, Cassino (FR), Italy.
Lermoyez syndrome (LS) has been regarded as a variant of Ménière's disease (MD), but so far there have been very few cases of LS reported in the literature, so such a conclusion is debatable. Specifying the pattern of auditory and vestibular changes at attack using objective quantitative measures is important for understanding the mechanism responsible for MD and LS. Here we report the first objective measures of dynamic otolith function and dynamic semicircular canal function in an LS patient at the time of the attack as well as at quiescence, documenting the fluctuation in otolith and semicircular canal function in the patient.
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