Assessment of the Membranous Labyrinth in Infants Using a Heavily T2-weighted 3D FLAIR Sequence without Contrast Agent Administration.


Journal

AJNR. American journal of neuroradiology
ISSN: 1936-959X
Titre abrégé: AJNR Am J Neuroradiol
Pays: United States
ID NLM: 8003708

Informations de publication

Date de publication:
01 2021
Historique:
received: 16 05 2020
accepted: 01 09 2020
pubmed: 30 1 2021
medline: 27 4 2021
entrez: 29 1 2021
Statut: ppublish

Résumé

Imaging is fundamental to assessing the acoustic pathway in infants with congenital deafness. We describe our depiction of the membranous labyrinth in infants using the heavily T2-weighted 3D FLAIR sequence without a contrast agent. We retrospectively reviewed 10 infants (20 ears) (median term equivalent age: 2 weeks; IQR: 1-5 weeks) who had undergone brain MR imaging including a noncontrast heavily T2-weighted 3D FLAIR scan of the temporal bone. For each ear, 3 observers analyzed, in consensus, the saccule, the utricle, and the 3 ampullae, assessing the visibility (score 0, not appreciable; score 1, visible without well-defined boundaries; score 2, visible with well-defined boundaries) and morphology ("expected" or "unexpected" compared with adults). The heavily T2-weighted 3D FLAIR sequence was scored for overall quality (score 0, inadequate; score 1, adequate but with the presence of image degradation; score 2, adequate). Six (60%) MR examinations were considered adequate (score 1 or 2). The saccule was visible in 10 ears (83.3%) with an expected morphology in 9 ears (90%). In 1 ear of an infant with congenital deafness, the saccule showed an unexpected morphology. The utricle was visible as expected in 12 ears (100%). The lateral ampulla was visible in 5 ears (41.6%), the superior ampulla was visible in 6 ears (50.0%), and the posterior ampulla was visible in 6 ears (50.0%), always with expected morphology (100%). MR imaging can depict the membranous labyrinth in infants using heavily T2-weighted 3D FLAIR without an injected contrast agent, but the sequence acquisition time reduces its feasibility in infants undergoing MR studies during natural sleep.

Sections du résumé

BACKGROUND AND PURPOSE
Imaging is fundamental to assessing the acoustic pathway in infants with congenital deafness. We describe our depiction of the membranous labyrinth in infants using the heavily T2-weighted 3D FLAIR sequence without a contrast agent.
MATERIALS AND METHODS
We retrospectively reviewed 10 infants (20 ears) (median term equivalent age: 2 weeks; IQR: 1-5 weeks) who had undergone brain MR imaging including a noncontrast heavily T2-weighted 3D FLAIR scan of the temporal bone. For each ear, 3 observers analyzed, in consensus, the saccule, the utricle, and the 3 ampullae, assessing the visibility (score 0, not appreciable; score 1, visible without well-defined boundaries; score 2, visible with well-defined boundaries) and morphology ("expected" or "unexpected" compared with adults). The heavily T2-weighted 3D FLAIR sequence was scored for overall quality (score 0, inadequate; score 1, adequate but with the presence of image degradation; score 2, adequate).
RESULTS
Six (60%) MR examinations were considered adequate (score 1 or 2). The saccule was visible in 10 ears (83.3%) with an expected morphology in 9 ears (90%). In 1 ear of an infant with congenital deafness, the saccule showed an unexpected morphology. The utricle was visible as expected in 12 ears (100%). The lateral ampulla was visible in 5 ears (41.6%), the superior ampulla was visible in 6 ears (50.0%), and the posterior ampulla was visible in 6 ears (50.0%), always with expected morphology (100%).
CONCLUSIONS
MR imaging can depict the membranous labyrinth in infants using heavily T2-weighted 3D FLAIR without an injected contrast agent, but the sequence acquisition time reduces its feasibility in infants undergoing MR studies during natural sleep.

Identifiants

pubmed: 33509916
pii: ajnr.A6876
doi: 10.3174/ajnr.A6876
pmc: PMC7872192
doi:

Substances chimiques

Contrast Media 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

377-381

Informations de copyright

© 2021 by American Journal of Neuroradiology.

Références

Acta Otolaryngol. 2010 Jun;130(6):665-9
pubmed: 19958242
Otol Neurotol. 2005 Sep;26(5):976-82
pubmed: 16151346
Neuroradiology. 2019 Apr;61(4):421-429
pubmed: 30719545
Magn Reson Med Sci. 2010;9(2):73-80
pubmed: 20585197
Clin Imaging. 2015 Jan-Feb;39(1):26-31
pubmed: 25457542
Pediatr Radiol. 2019 Apr;49(4):433-447
pubmed: 30923875
Nat Rev Dis Primers. 2017 Jan 12;3:16094
pubmed: 28079113
Neuroradiology. 1996 Apr;38(3):278-86
pubmed: 8741202
N Engl J Med. 2006 May 18;354(20):2151-64
pubmed: 16707752
Am J Hum Genet. 2005 Dec;77(6):945-57
pubmed: 16380907
AJNR Am J Neuroradiol. 2017 Oct;38(10):1998-2002
pubmed: 28751512
Pediatrics. 2007 Oct;120(4):898-921
pubmed: 17908777
Pediatr Radiol. 2018 Jul;48(7):992-998
pubmed: 29594440
AJNR Am J Neuroradiol. 2018 Nov;39(11):2114-2119
pubmed: 30337432
Eur J Radiol. 2018 Dec;109:77-82
pubmed: 30527315
Am J Med Genet. 1993 Jun 15;46(5):486-91
pubmed: 8322805
AJNR Am J Neuroradiol. 2008 Sep;29(8):1436-40
pubmed: 18388217
Magn Reson Med Sci. 2010;9(4):237-42
pubmed: 21187694
Acta Otorhinolaryngol Ital. 2018 Aug;38(4):369-376
pubmed: 30197428
Am J Otol. 2000 Jul;21(4):528-33
pubmed: 10912699
Pediatrics. 1998 Nov;102(5):1161-71
pubmed: 9794949
Acta Otolaryngol. 2010 Mar;130(3):338-43
pubmed: 19685358
Laryngoscope. 2008 Mar;118(3):501-5
pubmed: 18091332
J Proteome Res. 2017 May 5;16(5):1911-1923
pubmed: 28282143
J Clin Virol. 2008 Feb;41(2):57-62
pubmed: 17959414
Lancet. 2005 Mar 5-11;365(9462):879-90
pubmed: 15752533
Sci Rep. 2017 Jul 6;7(1):4825
pubmed: 28684743

Auteurs

G Conte (G)

From the Neuroradiology Unit (G.C., S.C., L.C., F.M.L.R., C.C., D.S., E.S., F.T.).

S Casale (S)

From the Neuroradiology Unit (G.C., S.C., L.C., F.M.L.R., C.C., D.S., E.S., F.T.).

L Caschera (L)

From the Neuroradiology Unit (G.C., S.C., L.C., F.M.L.R., C.C., D.S., E.S., F.T.) luca.caschera@policlinico.mi.it.

F M Lo Russo (FM)

From the Neuroradiology Unit (G.C., S.C., L.C., F.M.L.R., C.C., D.S., E.S., F.T.).

C Paolella (C)

Department of Advanced Biomedical Sciences (C.P.), University of Naples "Federico II," Naples, Italy.

C Cinnante (C)

From the Neuroradiology Unit (G.C., S.C., L.C., F.M.L.R., C.C., D.S., E.S., F.T.).

F Di Berardino (FD)

Audiology Unit (F.D.B., D.Z.).

D Zanetti (D)

Audiology Unit (F.D.B., D.Z.).

D Stocchetti (D)

From the Neuroradiology Unit (G.C., S.C., L.C., F.M.L.R., C.C., D.S., E.S., F.T.).

E Scola (E)

From the Neuroradiology Unit (G.C., S.C., L.C., F.M.L.R., C.C., D.S., E.S., F.T.).

L Bassi (L)

NICU (L.B.), Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano, Università degli Studi di Milano, Milan, Italy.

F Triulzi (F)

From the Neuroradiology Unit (G.C., S.C., L.C., F.M.L.R., C.C., D.S., E.S., F.T.).
Department of Pathophysiology and Transplantation (F.T.), University of Milan, Milan, Italy.

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