2020, Número 05
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Revista Médica Sinergia 2020; 5 (05)
Síndrome opsoclonus – mioclonus
Delgado CLG, Benavides VJD, Marín RGJ
Idioma: Español
Referencias bibliográficas: 19
Paginas: 420-420
Archivo PDF: 155.63 Kb.
RESUMEN
El síndrome opsoclonus-mioclonus es una condición rara, asociada con
una etiología de carácter autoinmune, tanto paraneoplásica, parainfecciosa
o idiopática. Estos pacientes se presentan con ataxia del tronco y
extremidades, con caídas, opsoclonus, mioclonías, y se puede acompañar
de diversos grados de encefalopatía, signos cerebelosos y alteraciones del
sueño. En el caso de la población pediátrica, se debe evaluar por
neuroblastoma; y en adultos con encefalopatía asociada se debe realizar
una evaluación exhaustiva para detectar malignidad oculta. Mientras que
los síntomas neurológicos agudos pueden controlarse mediante
inmunoterapia, y se ha visto respuesta parcial a tratamiento antitumoral, el
resultado a largo plazo se caracteriza por la presencia de déficit
neuropsicológico.
REFERENCIAS (EN ESTE ARTÍCULO)
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