In patients with demyelinating retrobulbar optic neuritis (RON), a spontaneous or corticosteroid-induced improvement is generally observed within the first month, but this is clinically insignificant in 5%-7% of patients. We report the case histories of four patients who were considered to be "non-responders" to corticosteroids because their visus remained unchanged or had improved by only 1/10 after one month from intravenous corticoid therapy begun 2-7 days after disease onset, and who were therefore subsequently administered high intravenous doses of immunoglobulin. Three of these patients completely recovered in a period of 3-9 months; the fourth showed only a partial improvement, but this was consolidated after long-term continuation of the same therapy. These cases suggest the possible efficacy of early administration of intravenous immunoglobulin in RON patients who fail to respond to cortisone therapy. As recently demonstrated in animal models, it can be hypothesised that the result is due to immuno-mediated mechanisms of action that reduce autoimmune responses in the short- and medium-term, and in the long-term favour remyelination.
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http://dx.doi.org/10.1007/BF03028812 | DOI Listing |
IDCases
October 2024
Department of Emergency Intensive Care Unit, Chengdu First People's Hospital, Chengdu, Sichuan, China.
Diagnostics (Basel)
October 2024
Clinical Neurosciences Department, "Carol Davila" University of Medicine and Pharmacy, 050474 Bucharest, Romania.
: This study investigated the frequency and timing of optic neuritis (ON) episodes in relation to the onset of multiple sclerosis (MS) and examined the occurrence of Uhthoff's phenomenon and Lhermitte's sign to understand their roles in early diagnosis and disease progression. : A longitudinal study was conducted with 127 MS patients. Clinical data, including ophthalmological examinations for ON, were collected and questionnaires assessed the presence of Uhthoff's phenomenon and Lhermitte's sign.
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September 2024
Multiple Sclerosis and Demyelinating Diseases Unit and Center of Expertise for Rare Demyelinating and Autoimmune Diseases of the Central Nervous System, 1st Department of Neurology, "Aeginition" University Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, GRC.
A unique case of a female adolescent diagnosed with myelin oligodendrocyte glycoprotein (MOG) monophasic optic neuritis with Epstein-Barr virus (EBV) reactivation antibody profile on a remote Greek island is presented, highlighting the challenges of diagnosing rare conditions in rural settings and the importance of connecting centers of expertise with regional hospitals. The 16-year-old patient presented with progressive vision loss, headache, and retrobulbar pain in the right eye. Initial ophthalmological examinations showed decreased visual acuity and color vision deterioration.
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August 2024
Ophthalmology, Dr. D. Y. Patil Medical College and Hospital, Pune, IND.
Int Ophthalmol
August 2024
Department of Ophthalmology, Health Science University Ankara Training and Researching Hospital, Ankara, Turkey.
Purpose: The study aims to investigate the demographic and neuroophthalmologic features of patients with multiple sclerosis (MS).
Methods: This retrospective study investigated 270 eyes of 135 patients with MS. All subjects underwent a full ophthalmological examination.
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