Cargando…

Unilateral Enlarged Vestibular Aqueduct Syndrome and Bilateral Endolymphatic Hydrops

Enlarged vestibular aqueduct (EVA) syndrome is a common congenital inner ear malformation characterized by a vestibular aqueduct with a diameter larger than 1.5 mm, mixed or sensorineural hearing loss that ranges from mild to profound, and vestibular disorders that may be present with a range from m...

Descripción completa

Detalles Bibliográficos
Autores principales: Ralli, Massimo, Nola, Giuseppe, Sparvoli, Luca, Ralli, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451758/
https://www.ncbi.nlm.nih.gov/pubmed/28607789
http://dx.doi.org/10.1155/2017/6195317
_version_ 1783240229685035008
author Ralli, Massimo
Nola, Giuseppe
Sparvoli, Luca
Ralli, Giovanni
author_facet Ralli, Massimo
Nola, Giuseppe
Sparvoli, Luca
Ralli, Giovanni
author_sort Ralli, Massimo
collection PubMed
description Enlarged vestibular aqueduct (EVA) syndrome is a common congenital inner ear malformation characterized by a vestibular aqueduct with a diameter larger than 1.5 mm, mixed or sensorineural hearing loss that ranges from mild to profound, and vestibular disorders that may be present with a range from mild imbalance to episodic objective vertigo. In our study, we present the case of a patient with unilateral enlarged vestibular aqueduct and bilateral endolymphatic hydrops (EH). EH was confirmed through anamnestic history and audiological exams; EVA was diagnosed using high-resolution CT scans and MRI images. Therapy included intratympanic infusion of corticosteroids with a significant hearing improvement, more evident in the ear contralateral to EVA. Although most probably unrelated, EVA and EH may present with similar symptoms and therefore the diagnostic workup should always include the proper steps to perform a correct diagnosis. Association between progression of hearing loss and head trauma in patients with a diagnosis of EVA syndrome is still uncertain; however, these individuals should be advised to avoid activities that increase intracranial pressure to prevent further hearing deterioration. Intratympanic treatment with steroids is a safe and well-tolerated procedure that has demonstrated its efficacy in hearing, tinnitus, and vertigo control in EH.
format Online
Article
Text
id pubmed-5451758
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-54517582017-06-12 Unilateral Enlarged Vestibular Aqueduct Syndrome and Bilateral Endolymphatic Hydrops Ralli, Massimo Nola, Giuseppe Sparvoli, Luca Ralli, Giovanni Case Rep Otolaryngol Case Report Enlarged vestibular aqueduct (EVA) syndrome is a common congenital inner ear malformation characterized by a vestibular aqueduct with a diameter larger than 1.5 mm, mixed or sensorineural hearing loss that ranges from mild to profound, and vestibular disorders that may be present with a range from mild imbalance to episodic objective vertigo. In our study, we present the case of a patient with unilateral enlarged vestibular aqueduct and bilateral endolymphatic hydrops (EH). EH was confirmed through anamnestic history and audiological exams; EVA was diagnosed using high-resolution CT scans and MRI images. Therapy included intratympanic infusion of corticosteroids with a significant hearing improvement, more evident in the ear contralateral to EVA. Although most probably unrelated, EVA and EH may present with similar symptoms and therefore the diagnostic workup should always include the proper steps to perform a correct diagnosis. Association between progression of hearing loss and head trauma in patients with a diagnosis of EVA syndrome is still uncertain; however, these individuals should be advised to avoid activities that increase intracranial pressure to prevent further hearing deterioration. Intratympanic treatment with steroids is a safe and well-tolerated procedure that has demonstrated its efficacy in hearing, tinnitus, and vertigo control in EH. Hindawi 2017 2017-05-18 /pmc/articles/PMC5451758/ /pubmed/28607789 http://dx.doi.org/10.1155/2017/6195317 Text en Copyright © 2017 Massimo Ralli et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ralli, Massimo
Nola, Giuseppe
Sparvoli, Luca
Ralli, Giovanni
Unilateral Enlarged Vestibular Aqueduct Syndrome and Bilateral Endolymphatic Hydrops
title Unilateral Enlarged Vestibular Aqueduct Syndrome and Bilateral Endolymphatic Hydrops
title_full Unilateral Enlarged Vestibular Aqueduct Syndrome and Bilateral Endolymphatic Hydrops
title_fullStr Unilateral Enlarged Vestibular Aqueduct Syndrome and Bilateral Endolymphatic Hydrops
title_full_unstemmed Unilateral Enlarged Vestibular Aqueduct Syndrome and Bilateral Endolymphatic Hydrops
title_short Unilateral Enlarged Vestibular Aqueduct Syndrome and Bilateral Endolymphatic Hydrops
title_sort unilateral enlarged vestibular aqueduct syndrome and bilateral endolymphatic hydrops
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451758/
https://www.ncbi.nlm.nih.gov/pubmed/28607789
http://dx.doi.org/10.1155/2017/6195317
work_keys_str_mv AT rallimassimo unilateralenlargedvestibularaqueductsyndromeandbilateralendolymphatichydrops
AT nolagiuseppe unilateralenlargedvestibularaqueductsyndromeandbilateralendolymphatichydrops
AT sparvoliluca unilateralenlargedvestibularaqueductsyndromeandbilateralendolymphatichydrops
AT ralligiovanni unilateralenlargedvestibularaqueductsyndromeandbilateralendolymphatichydrops