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Erschienen in: Journal of Neurology 1/2014

01.01.2014 | Original Communication

Differential diagnoses to MS: experiences from an optic neuritis clinic

verfasst von: Henrik Horwitz, Tina Friis, Signe Modvig, Hanne Roed, Anna Tsakiri, Bjarne Laursen, Jette Lautrup Frederiksen

Erschienen in: Journal of Neurology | Ausgabe 1/2014

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Abstract

Optic neuritis (ON) is closely linked to multiple sclerosis (MS). It may, however, also be associated to a range of autoimmune or infectious diseases. The purpose of this study was to assess the differential diagnoses in patients with suspected ON. In this retrospective study, we reviewed the files of all patients referred to the Clinic of Optic Neuritis, Glostrup Hospital, University of Copenhagen, Denmark, between January 2000 and November 2011. All patients were referred by ophthalmologists with possible ON. Patients diagnosed with MS prior to referral were excluded from the study. A total of 643 patients were included in the study. Apart from ON, the most frequent diagnoses were tumors (n = 15), ischemic or hypertensive neuropathies (n = 13), and retinal or choroid disorders (n = 9). Six patients were diagnosed with neuromyelitis optica. Rarer causes of visual loss were infections (n = 5), giant cell arteritis (n = 4), sarcoidosis (n = 3), thyrotoxicosis (n = 2), and hereditary or toxic neuropathies (n = 2). Nine percent of patients referred to the Clinic of Optic Neuritis had symptoms caused by medical, neurosurgical or ophthalmic disorders, and 0.9 % of our patients had NMO. Though most of these conditions are rare, it is of importance to keep them in mind upon encountering patients with symptoms of ON.
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Metadaten
Titel
Differential diagnoses to MS: experiences from an optic neuritis clinic
verfasst von
Henrik Horwitz
Tina Friis
Signe Modvig
Hanne Roed
Anna Tsakiri
Bjarne Laursen
Jette Lautrup Frederiksen
Publikationsdatum
01.01.2014
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Neurology / Ausgabe 1/2014
Print ISSN: 0340-5354
Elektronische ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-013-7166-x

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