1. Papilledema and Peripheral Neuropathies
- Author
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Jean-Michel Vallat, Clément Baron, Jonathan Ciron, Gwendal Le Masson, Irina Balaboi, Guilhem Solé, Stéphane Mathis, Louis Carla, M. Boissonnot, Antoine Soulages, Louis Nadal, Fanny Duval, Thomas Bonduelle, and Thomas Lathière
- Subjects
Adult ,Male ,medicine.medical_specialty ,Adolescent ,Intracranial Pressure ,030204 cardiovascular system & hematology ,Guillain-Barre Syndrome ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Peripheral nerve ,medicine ,Humans ,Papilledema ,Child ,Intracranial pressure ,Aged ,business.industry ,Autoantibody ,Polyradiculoneuropathy ,General Medicine ,Middle Aged ,medicine.disease ,Dermatology ,eye diseases ,Pathophysiology ,Peripheral ,Child, Preschool ,Female ,Neurology (clinical) ,Bilateral papilledema ,medicine.symptom ,business ,030217 neurology & neurosurgery - Abstract
Introduction Papilledema is a common sign in ophthalmology and is typically associated with increased intracranial pressure (ICP) in neurological diseases. Since the beginning of the 20th century, some cases of papilledema have been reported in association with acute or chronic inflammatory neuropathies. Case report We describe a 42-year-old man with acute-onset inflammatory polyradiculoneuropathy and bilateral papilledema. Conclusions Based on a personal case report and from an extensive review of the medical literature, we identify 2 distinct patterns. First, radiculoneuropathy may be a consequence of intracranial pressure (peripheral nerve involvement corresponding to a "false localizing sign"). Second, papilledema may occur after the onset of inflammatory neuropathy. For such cases, the pathophysiological mechanism remains unknown (eg, reactional inflammatory processes or actions of unknown autoantibodies) and requires further elucidation.
- Published
- 2019