Histological characteristics of intra-temporal facial nerve paralysis in temporal bone malignancies.
Facial nerve paralysis
otopathology
temporal bone histology
temporal bone histopathology
temporal bone malignancy
Journal
The Laryngoscope
ISSN: 1531-4995
Titre abrégé: Laryngoscope
Pays: United States
ID NLM: 8607378
Informations de publication
Date de publication:
05 2020
05 2020
Historique:
received:
04
03
2019
revised:
06
06
2019
accepted:
10
07
2019
pubmed:
2
8
2019
medline:
26
8
2020
entrez:
2
8
2019
Statut:
ppublish
Résumé
To describe the histopathologic findings and clinical presentation of intra-temporal facial nerve invasion in primary and metastatic malignancies of the human temporal bone (TB). Retrospective analysis of all medical records of patients diagnosed with peripheral facial nerve palsy (PFnP) of a malignant origin was performed. Temporal bones underwent standard processing for histologic examination. Hematoxylin and eosin (H&E)-stained slides were examined by light microscopy. The histologic findings were compared to premortem clinical data. Eighteen TBs were identified in 16 patients. The male to female ratio was 9:7. The median (range) age of death was 56.5 years (27 months to 75 years). The median time interval from facial nerve injury to death was 5.5 months. There were 11 carcinomas and seven sarcomas identified. Primary TB malignancies were identified in seven TBs (39%), and the rest (11 TBs, 61%) were of metastatic origin. Complete facial nerve paralysis (House-Brackmann [HB] grade VI), was the most common clinical presentation affecting nine patients (10 TBs, 56%). Neural involvement was multifocal in nature (16 of 18 TBs, 89%). The most commonly involved cranial nerve (CN) VII segment was the meatal segment (13 TBs, 72%), followed by the labyrinthine, tympanic, and vertical segments (nine, eight, and six TBs, respectively). PFnP can be the result of local, regional, or distant malignancy, and is associated with poor survival. The facial nerve can serve as a route of tumor progression intracranially. Whereas every segment of CNV II can be violated by tumors, not all PFnP are related to direct tumor invasion. 4 Laryngoscope, 130:E358-E367, 2020.
Identifiants
pubmed: 31369154
doi: 10.1002/lary.28212
pmc: PMC7425210
mid: NIHMS1614287
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
E358-E367Subventions
Organisme : NCI NIH HHS
ID : P01 CA240239
Pays : United States
Informations de copyright
© 2019 The American Laryngological, Rhinological and Otological Society, Inc.
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