Temporal bone histopathology in MELAS syndrome.

MELAS syndrome genetics otology otopathology sensorineural hearing loss

Journal

Laryngoscope investigative otolaryngology
ISSN: 2378-8038
Titre abrégé: Laryngoscope Investig Otolaryngol
Pays: United States
ID NLM: 101684963

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 07 10 2019
revised: 26 11 2019
accepted: 24 12 2019
entrez: 5 3 2020
pubmed: 5 3 2020
medline: 5 3 2020
Statut: epublish

Résumé

Describe the histopathology of the temporal bones in MELAS (myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) syndrome. The syndrome results from a known point mutation in mitochondrial DNA. Histopathology analysis of a pair of temporal bones from the oldest surviving MELAS syndrome temporal bone donor. Histopathologic findings were correlated with known premortem clinical data. The inner ears showed severe but incomplete atrophy of the stria vascularis for the length of the cochleae. In contrast, the organ of Corti and inner hair cells appeared intact with some loss of outer hair cells. Other than moderate loss at the basal turn, spiral ganglion cells numbers were normal. The vestibular neuroepithelium was mostly normal with the exception of moderate degeneration of the macula sacculi and partial collapse of the saccular wall on the right. The cerebral cortex had infarct-like lesions with adjacent gliosis. This is an analysis of the oldest patient with MELAS syndrome to date, an addition to only two previously published patients. It supports the notion that hearing loss is a result of dysfunction of the stria vascularis and not loss of hair cells or neurons. Patterns of vestibular pathology are in agreement to in-vivo measurements. These findings support auditory rehabilitation with cochlear implants and may be relevant to hearing loss due to other mitochondrial mutations. 4.

Identifiants

pubmed: 32128442
doi: 10.1002/lio2.344
pii: LIO2344
pmc: PMC7042650
doi:

Types de publication

Journal Article

Langues

eng

Pagination

152-156

Subventions

Organisme : NIDCD NIH HHS
ID : U24 DC013983
Pays : United States

Informations de copyright

© 2020 The Authors. Laryngoscope Investigative Otolaryngology published by Wiley Periodicals, Inc. on behalf of The Triological Society.

Déclaration de conflit d'intérêts

The authors declare no potential conflict of interest.

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Auteurs

Ophir Handzel (O)

Cochlear Implant Center, Department of Otolaryngology/Head, Neck & Maxillofacial Surgery Tel-Aviv Sourasky Medical Center, Sackler Faculty of Medicine Tel-Aviv University Israel.

Omer J Ungar (OJ)

Department of Otolaryngology/Head, Neck & Maxillofacial Surgery Tel-Aviv Sourasky Medical Center, Sackler Faculty of Medicine Tel-Aviv University Israel.

Dan J Lee (DJ)

Otopathology Laboratory, Department of Otolaryngology-Head and Neck Surgery, Massachusetts Eye and Ear Harvard Medical School Boston Massachusetts.

Joseph B Nadol (JB)

Otopathology Laboratory, Department of Otolaryngology-Head and Neck Surgery, Massachusetts Eye and Ear Harvard Medical School Boston Massachusetts.

Classifications MeSH