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Concurrent superior semicircular canal dehiscence and endolymphatic hydrops: A novel case series

INTRODUCTION: Superior semicircular canal dehiscence (SSCD) is characterized by CT-confirmed bony erosion over the superior semicircular canal, creating vestibular and auditory symptoms. Endolymphatic hydrops (EH) is characterized by an MRI-confirmed excess of endolymph within the scala media that d...

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Autores principales: Johanis, Michael, De Jong, Russell, Miao, Tyler, Hwang, Leslie, Lum, Meachelle, Kaur, Taranjit, Willis, Shelby, Arsenault, John J., Duong, Courtney, Yang, Isaac, Gopen, Quinton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804363/
https://www.ncbi.nlm.nih.gov/pubmed/33421957
http://dx.doi.org/10.1016/j.ijscr.2020.12.074
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author Johanis, Michael
De Jong, Russell
Miao, Tyler
Hwang, Leslie
Lum, Meachelle
Kaur, Taranjit
Willis, Shelby
Arsenault, John J.
Duong, Courtney
Yang, Isaac
Gopen, Quinton
author_facet Johanis, Michael
De Jong, Russell
Miao, Tyler
Hwang, Leslie
Lum, Meachelle
Kaur, Taranjit
Willis, Shelby
Arsenault, John J.
Duong, Courtney
Yang, Isaac
Gopen, Quinton
author_sort Johanis, Michael
collection PubMed
description INTRODUCTION: Superior semicircular canal dehiscence (SSCD) is characterized by CT-confirmed bony erosion over the superior semicircular canal, creating vestibular and auditory symptoms. Endolymphatic hydrops (EH) is characterized by an MRI-confirmed excess of endolymph within the scala media that distorts the membranous labyrinth. While there is overlap in symptoms, the two diseases result from different pathophysiologies and require different interventions. PRESENTATION OF CASES: A retrospective chart review was conducted at the University of California, Los Angeles on a database of 270 adult SSCD patients, gathered between March 2011 and February 2020. A review of clinical notes, post-operative findings, and imaging was performed for 16 patients who had both CT-confirmed SSCD and an MRI of the internal auditory canal (IAC). Three cases of concurrent SSCD and EH were identified. Medical and surgical history, symptom progression pre- and post-operatively, and treatment outcomes were gathered. One patient’s symptoms were resolved via mycophenolate mofetil, another’s via hydrochlorothiazide, and the third’s via hydrochlorothiazide and bilateral hearing aids. DISCUSSION: Post-surgical persistence of SSCD symptoms that are mutually shared with EH is the strongest indicator that a physician should investigate for concurrent EH. VEMP and audiogram testing in these cases can be misleading and should not be relied on as rule-in or rule-out tests. CONCLUSION: Concurrent SSCD and EH is a rare but treatable entity. Physicians should consider ordering an MRI of the IAC if SSCD patients’ symptoms persist or recur after a successful surgery.
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spelling pubmed-78043632021-01-22 Concurrent superior semicircular canal dehiscence and endolymphatic hydrops: A novel case series Johanis, Michael De Jong, Russell Miao, Tyler Hwang, Leslie Lum, Meachelle Kaur, Taranjit Willis, Shelby Arsenault, John J. Duong, Courtney Yang, Isaac Gopen, Quinton Int J Surg Case Rep Case Series INTRODUCTION: Superior semicircular canal dehiscence (SSCD) is characterized by CT-confirmed bony erosion over the superior semicircular canal, creating vestibular and auditory symptoms. Endolymphatic hydrops (EH) is characterized by an MRI-confirmed excess of endolymph within the scala media that distorts the membranous labyrinth. While there is overlap in symptoms, the two diseases result from different pathophysiologies and require different interventions. PRESENTATION OF CASES: A retrospective chart review was conducted at the University of California, Los Angeles on a database of 270 adult SSCD patients, gathered between March 2011 and February 2020. A review of clinical notes, post-operative findings, and imaging was performed for 16 patients who had both CT-confirmed SSCD and an MRI of the internal auditory canal (IAC). Three cases of concurrent SSCD and EH were identified. Medical and surgical history, symptom progression pre- and post-operatively, and treatment outcomes were gathered. One patient’s symptoms were resolved via mycophenolate mofetil, another’s via hydrochlorothiazide, and the third’s via hydrochlorothiazide and bilateral hearing aids. DISCUSSION: Post-surgical persistence of SSCD symptoms that are mutually shared with EH is the strongest indicator that a physician should investigate for concurrent EH. VEMP and audiogram testing in these cases can be misleading and should not be relied on as rule-in or rule-out tests. CONCLUSION: Concurrent SSCD and EH is a rare but treatable entity. Physicians should consider ordering an MRI of the IAC if SSCD patients’ symptoms persist or recur after a successful surgery. Elsevier 2020-12-26 /pmc/articles/PMC7804363/ /pubmed/33421957 http://dx.doi.org/10.1016/j.ijscr.2020.12.074 Text en © 2021 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Series
Johanis, Michael
De Jong, Russell
Miao, Tyler
Hwang, Leslie
Lum, Meachelle
Kaur, Taranjit
Willis, Shelby
Arsenault, John J.
Duong, Courtney
Yang, Isaac
Gopen, Quinton
Concurrent superior semicircular canal dehiscence and endolymphatic hydrops: A novel case series
title Concurrent superior semicircular canal dehiscence and endolymphatic hydrops: A novel case series
title_full Concurrent superior semicircular canal dehiscence and endolymphatic hydrops: A novel case series
title_fullStr Concurrent superior semicircular canal dehiscence and endolymphatic hydrops: A novel case series
title_full_unstemmed Concurrent superior semicircular canal dehiscence and endolymphatic hydrops: A novel case series
title_short Concurrent superior semicircular canal dehiscence and endolymphatic hydrops: A novel case series
title_sort concurrent superior semicircular canal dehiscence and endolymphatic hydrops: a novel case series
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804363/
https://www.ncbi.nlm.nih.gov/pubmed/33421957
http://dx.doi.org/10.1016/j.ijscr.2020.12.074
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