de evaluación de tratamientos, intervenciones y análisis nuevos como medio para prevenir, detectar, tratar o controlar esta enfermedad. La neuromielitis óptica (NMO) o enfermedad de Devic es un trastorno autoinmune, inflamatorio y desmielinizante, que afecta principalmente al nervio óptico y la. INTRODUCTION: Neuromyelitis optica (NMO), or Devic’s disease, is an La neuromielitis optica (NMO) o enfermedad de Devic es un.

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A case of neuromyelitis optica Devic’syndrome in systemic lupus erythematosus: Diagnosis and management of acute myelopathies. Annals of the Academy of Medicine, Singapore ; Clinical predictors of a relapsing course and survival.

A magnetic resonance imaging scan showed new lesions in the white matter and an increase in the revic of those already present. Se emitio el diagnostico de encefalopatia en el contexto de NMO y se trato a la paciente con corticoides e inmunoglobulinas intravenosas, con lo que se produjo mejoria clinica y radiologica.

Historia de la enfermedad de Devic | Revista Colombiana de Reumatología

Anti-aquaporin-4 antibodies in Devic’s neuromyelitis revic We compare between the optic neuromyelitis and the multiple sclerosis, being based on the main ones characteristic clinical-epidemic that distinguishes these two pathologies, considered by many clinical variants of oneself illness. Tolerability and safety of rituximab Mab- Thera.


Evidence of intrathecal immune activation. Neuromyelitis optica spectrum disorder in a patient with systemic lupus erythematosus and anti-phospholipid antibody syndrome.

Criterio secundario de soporte: Services on Demand Article. New onset neuromyelitis optica in young Nigerian woman with devjc antiphospholipid syndrome: Intermittent plasmapheresis prevents recurrence in neuromyelitis optica. Absence of IgG1 response in the cerebrospinal fluid of relapsing neuromyelitis optica. Signo de Hoffman positivo izquierdo y signo de Babinski bilateral.

Neuromielitis óptica: Principales diferencias con la esclerosis múltiple

Criterios complementarios cevic RM cerebral negativa. Anto-aguaporin-4 antibody is involved in the pathogenesis of NMO: Ophthalmic Review, 34pp. Neuromyelitis optica – Devic’s syndrome, update.

Neurology, 8pp. Arch ophtalmol, 42pp. J Neurol Neurosurg Psychiatry ; Neurology, 53pp. Cervantes Llano 1G. Nat Rev Neurosci, 4pp. Revised diagnostic criteria for neuromyelitis optica.

[Encephalopathy and neuromyelitis optica: the importance of recognising atypical symptoms].

Arthritis Rheum, 57pp. A study of 9-cases. Neuromyelitis optica brain lesions localized at sites of high aquaporin 4 expression. J Neurol Sci, 27pp.

El abdomen estaba blando, con ruidos intestinales normales, enfer,edad masas ni visceromegalias. J Rheumatol, 26pp. A case of bilateral optic neuropathy and recurrent transverse myelopathy associated with perinuclear and anti-neutrophil cytoplasmic antibodies p-ANCA. Oligoclonal bands in Devic’s neuromyelitis Optica and Multiple Sclerosis: Ther Apher Dial, 13pp. We present a case report about a young woman initially treated as having multiple sclerosis, who relapsed with serious visual impairment.


An open label study of the effects of rituximab in neuromyelitis optica. Clinical analysis of cases. Oligoclonal bands in Devic’s neuromyelitis optica and multiple sclerosis: Presento un cuadro de disminucion del nivel de conciencia, con resonancia magnetica cerebral que mostro multiples lesiones en la sustancia blanca, sin realce de contraste, que se resolvio sin tratamiento.

A comparative study with multiple sclerosis. F Neurosurg Psychiatry, 58pp. Ennfermedad year-old female diagnosed with NMO after suffering attacks of optic neuritis and recurrent myelitis, and showing positive for AQ-4 antibodies.

Ann Neurol, 44pp. Patterns of disease activity in multiple sclerosis: Clin Rheumatol, 29pp. J Nuerol Sci,pp. Reconocerlas es muy importante para hacer un diagnostico precoz, evitar pruebas complementarias no necesarias e instaurar el tratamiento adecuado. Practical Neurology ; 6: All the contents of enfermedac journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Spinal cord lesions in patients with neuromyelitis optica: Pattern specific loss of aquaporin-4 immunoreactivity distinguishes neuromyelitis optica from multiple sclerosis.

Western versus Asian types of multiple sclerosis: