Concurrent superior semicircular canal dehiscence and endolymphatic hydrops: A novel case series.
CT
Case series
Endolymphatic hydrops
MRI
Meniere’s disease
Superior semicircular canal dehiscence
Journal
International journal of surgery case reports
ISSN: 2210-2612
Titre abrégé: Int J Surg Case Rep
Pays: Netherlands
ID NLM: 101529872
Informations de publication
Date de publication:
Jan 2021
Jan 2021
Historique:
received:
29
11
2020
revised:
22
12
2020
accepted:
22
12
2020
pubmed:
10
1
2021
medline:
10
1
2021
entrez:
9
1
2021
Statut:
ppublish
Résumé
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. 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. 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. 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.
Identifiants
pubmed: 33421957
pii: S2210-2612(20)31264-5
doi: 10.1016/j.ijscr.2020.12.074
pmc: PMC7804363
pii:
doi:
Types de publication
Journal Article
Langues
eng
Pagination
382-386Informations de copyright
Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.
Références
Int J Surg. 2018 Dec;60:279-282
pubmed: 30359781
J Clin Neurosci. 2017 Sep;43:103-107
pubmed: 28622893
Eur Arch Otorhinolaryngol. 2020 Aug 14;:
pubmed: 32797276
J Neurol. 2016 Apr;263 Suppl 1:S71-81
pubmed: 27083887
Otol Neurotol. 2018 Feb;39(2):e123-e130
pubmed: 29315188
Acta Otolaryngol. 2006 Oct;126(10):1030-5
pubmed: 16923705
Acta Otolaryngol. 2015;135(10):974-7
pubmed: 26107020
Otolaryngol Clin North Am. 2010 Oct;43(5):971-83
pubmed: 20713237
J Clin Neurosci. 2019 Aug;66:128-132
pubmed: 31103254
Arch Otolaryngol Head Neck Surg. 2000 Feb;126(2):137-47
pubmed: 10680863
Audiol Neurootol. 2010;15(5):318-22
pubmed: 20173319
Am J Otol. 2000 Jan;21(1):9-19
pubmed: 10651428
Front Neurol. 2017 Apr 28;8:177
pubmed: 28503164
Arch Otolaryngol Head Neck Surg. 1998 Mar;124(3):249-58
pubmed: 9525507
Neurology. 2014 Mar 18;82(11):1010
pubmed: 24638216
J Clin Neurosci. 2018 Aug;54:109-112
pubmed: 29908720
Otol Neurotol. 2007 Oct;28(7):920-926
pubmed: 17704722
Sci Rep. 2015 Oct 12;5:14951
pubmed: 26455332
Int J Surg. 2020 Dec;84:231-235
pubmed: 33189880