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Successful Management of Acute Streptococcal Meningoencephalitis Complicated by Bilateral Third-Nerve Palsies, Wall-Eyed Bilateral Internuclear Ophthalmoplegia, Blindness, and Deafness: Case Report

Authors :
Amitouj S. Sidhu
Charles E.L. Walker
Thomas D. Riisfeldt
Peter J. Tweedie
Natasha Gerbis
Emily J. Sutherland
Neil G. Simon
Lucy K. Somerville
Ross Bradbury
Raymond Cook
Jonathon Parkinson
Robert Goetti
Ian C. Francis
Source :
Case Reports in Ophthalmology, Vol 15, Iss 1, Pp 423-429 (2024)
Publication Year :
2024
Publisher :
Karger Publishers, 2024.

Abstract

Introduction: Streptococcal meningoencephalitis (SME) is a rare, and frequently lethal, acute infection, and inflammation of the central nervous system parenchyma, with associated meningeal involvement. Bacterial meningoencephalitis is generally associated with high rates of morbidity and mortality, despite available antimicrobial and corticosteroid treatments. While Streptococcus pneumoniae is well recognised to cause bacterial meningitis, direct extension into the central nervous system parenchyma is rare. Case Presentation: A previously well 49-year-old man presented with sudden onset severe headache, fevers, neck stiffness, and reduced consciousness. The manifestations of SME in this patient were bilateral pupil-involving third-nerve palsies, wall-eyed bilateral internuclear ophthalmoplegia (WEBINO), bilateral blindness, bilateral deafness, a right lower motor neuron facial palsy, and upper motor neuron signs in his limbs. Initially, a partial response to high dose intravenous antibiotics occurred, but with administration of intravenous corticosteroids, further substantial resolution of the patient’s neurological and neuro-ophthalmological deficits occurred. Conclusion: This case highlights the benefit of multidisciplinary diagnostic and therapeutic interventions in a case of SME complicated by bilateral pupil-involving third-nerve palsies, WEBINO, bilateral blindness, bilateral deafness, a right lower motor neuron facial palsy, and upper motor neuron signs. It appears to be the first reported case of SME with this rare collection of neuro-ophthalmological abnormalities.

Details

Language :
English
ISSN :
16632699
Volume :
15
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Case Reports in Ophthalmology
Publication Type :
Academic Journal
Accession number :
edsdoj.51f405c1d604905927d4939a6d218f9
Document Type :
article
Full Text :
https://doi.org/10.1159/000538821