dc.creatorCartier Rovirosa, Luis
dc.creatorArellano C, Roberto
dc.creatorGarcia F, Luis
dc.creatorAraya D, Fernando
dc.creatorCampero S, Mario
dc.date.accessioned2019-01-29T17:16:01Z
dc.date.available2019-01-29T17:16:01Z
dc.date.created2019-01-29T17:16:01Z
dc.date.issued1998
dc.identifierRevista Medica de Chile, Volumen 126, Issue 8, 2018, Pages 981-986
dc.identifier00349887
dc.identifierhttps://repositorio.uchile.cl/handle/2250/163387
dc.description.abstractOptic neuromyelitis is characterized by simultaneous or successive necrotizing lesions involving the optic nerves and the spinal cord. We report two females with the disease, aged 30 and 34 years old. In the latter, a neuropathological study was done. Both patients had clinical, neuroradiological and pathological features that differed from those of primary demyelinating syndromes such as multiple sclerosis. These patients illustrate the selectivity of optic nerve and spinal cord lesions. The latter involve mainly pyramidal and Goll tracts while, within the necrotizing lesions of the optic chiasma, the fibers of the unaffected optic nerve are spared. This pattern suggests a selective injury to some population of axons. Blood vessels were not affected in the necrotizing areas and the lesions did not follow a vascular territory, therefore a vascular mechanism causing the disease is unlikely. The clinical and neuropathological features of neuromyelitis optic suggest a selective involvemen
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceRevista Medica de Chile
dc.subjectNerve degeneration
dc.subjectNeurology
dc.subjectNeuromyelitis optic
dc.subjectOptic nervodiseases
dc.titleNeuromyelitis optic, a necrotizing disease of the Central Nervous System. Report of two cases Neuromielitis óptica: Una enfermedad necrotizante del Sistema Nervioso Central
dc.typeArtículo de revista


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