Mod Rheumatol Case Rep
Division of Immunology and Rheumatology, Third Department of Internal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan.
Published: March 2025
Immunoglobulin G4-related disease (IgG4-RD) is a systemic rheumatic disease characterized by the infiltration of IgG4-positive plasma cells and swelling or hypertrophic lesions in various organs. IgG4-RD also involves optic lesions, which is known as IgG4-related ophthalmic disease (IgG4-ROD). IgG4-ROD involves the surrounding tissues, causing optic neuropathy when it affects the optic nerve. Impairment of the optic nerve is often progressive, with delayed diagnosis and treatment leading to permanent visual loss. However, optic neuropathy due to IgG4-RD is rare and the visual prognosis is unclear. Herein, we present a case of long-standing optic neuropathy in IgG4-ROD with loss of light perception.
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http://dx.doi.org/10.1093/mrcr/rxaf015 | DOI Listing |
BMJ Case Rep
March 2025
Radiology, King's College London, London, UK.
A boy in middle childhood with a history of early morning headaches presented to secondary care after being found to have bilateral papilloedema by his community optometrist. CT head showed a large right-sided heterogeneous calcific and haemorrhagic mass causing marked mass effect and midline shift. Preoperatively, the lesion was characterised on MRI as a haemorrhagic mass with a 'popcorn' appearance suggestive of a giant cavernous malformation measuring 6.
View Article and Find Full Text PDFNeurol Neuroimmunol Neuroinflamm
May 2025
Department of Neurology, University Hospital of Marseille, France.
Background And Objectives: A simple, quick, and reproducible procedure for distinguishing multiple sclerosis (MS), myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), and neuromyelitis optica spectrum disorder (NMOSD) at inaugural optic neuritis (ION) could be highly valuable in guiding early management.
Methods: We included all adults admitted to the MS center of Marseille for ION between March 2016 and April 2024, with CSF analysis including the kappa free light chain (K-FLC) index. Receiver operating characteristic curves were used to measure the diagnostic ability of the K-FLC index.
Front Cell Dev Biol
February 2025
Department of Clinical and Biological Sciences & Neuroscience Institute Cavalieri Ottolenghi (NICO), University of Torino, Torino, Italy.
Introduction: Recent evidence supports the hypothesis of an association between gut microbiota and the pathogenesis of retinal and eye diseases, suggesting the existence of a gut-eye axis. However, no data are available on the possible effect of the gut microbiota on the optic nerve fiber maturation and myelin development.
Methods: We investigated the impact of gut microbiota on the optic nerves collected from neonatal and young adult germ-free (GF), gnotobiotic (stably colonized with 12 bacteria strains, OMM12) and control (colonized with a complex gut microbiota, CGM) mice, by performing stereological and morphoquantitative analyses with transmission electron microscopy and gene expression analysis by quantitative real-time PCR.
Pract Neurol
March 2025
Department of Brain Repair & Rehabilitation, Institute of Neurology, University College London, London, UK.
Graefes Arch Clin Exp Ophthalmol
March 2025
Sunderland Eye Infirmary, NHS Trust, Sunderland, UK & Biosciences Institute, Newcastle University, Newcastle Upon Tyne, UK.
Purpose: Primary epiretinal, or more precisely termed pre macular membranes (PMM) and glaucomatous optic neuropathy are both common conditions affecting a predominantly elderly population. There are several relevant clinical and pathological considerations when they are both diagnosed in the same eye.
Methods: We systematically searched the literature to review the challenges clinicians must address when dealing with patients with co-existing PMM and glaucoma.
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