Bilateral palsy of the hypoglossal nerve following general anesthesia for emergency surgery. A case report.
Airway
Case report
Complications
Intubation
Neuropathy
Position
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:
Jul 2022
Jul 2022
Historique:
received:
16
06
2022
revised:
30
06
2022
accepted:
01
07
2022
pubmed:
9
7
2022
medline:
9
7
2022
entrez:
8
7
2022
Statut:
ppublish
Résumé
Hypoglossal nerve palsy is a rare condition usually associated with tumors, trauma, stroke or multiple sclerosis. It can be associated with other cranial nerve palsies while injury to this nerve typically affects a patient's articulation by causing lingual motility disturbance and swallowing difficulty. Bilateral isolated hypoglossal nerve palsy is an even more infrequent condition, which can occasionally be due to airway manipulation. We describe a case of bilateral hypoglossal nerve damage following general anesthesia for emergency surgery, presenting with dysarthria, immobility of the tongue and dysphagia after extubation. The patient had a gradual recovery of all lost functions during the next four months. Bilateral hypoglossal nerve palsy is a very rare entity and tracheal tube malposition or prolonged but unnoticed tracheal cuff pressure especially in the face of low blood pressure, should be considered as possible causative mechanisms for this condition. This underlines the importance of careful positioning of the patient's head and neck during surgery as well as the meticulous and correct performance of routine maneuvers of airway management. Bilateral hypoglossal nerve palsy is a very rare entity. Diagnosis and management of twelfth nerve palsy require a multidisciplinary approach to achieve the best patient outcome.
Identifiants
pubmed: 35803095
pii: S2210-2612(22)00633-2
doi: 10.1016/j.ijscr.2022.107387
pmc: PMC9284038
pii:
doi:
Types de publication
Journal Article
Langues
eng
Pagination
107387Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.