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Headache Associated with Moyamoya Disease in a Child: Pain Pattern in MRA Progression / 대한소아신경학회지
Article en En | WPRIM | ID: wpr-23608
Biblioteca responsable: WPRO
ABSTRACT
Headache associated with moyamoya disease (HAMD) has been reported in about 20-30% of pediatric cases with moyamoya disease. However, the characteristic patterns of HAMD during disease progression are not completely known, although much is known on the incidence of HAMD and on the treatment effects of bypass surgery. In a child who presented with HAMD and had no infarction or hemorrhage till bypass surgery, we described the characteristic patterns of headache progression. At first presentation, the patient complained of severe bilateral headache despite mild stenosis only in the left internal carotid artery on brain magnetic resonance angiography. During all stages of progression, headache was severe and pressing in nature rather than throbbing. Nausea and vomiting were present even in the early stage, but photophobia, phonophobia and neck stiffness developed in the late stage. Headache was aggravated by menstruation and was relieved by analgesics and topiramate in the early stage, although the medication failed to provide relief when the headache increased in frequency and duration.
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Texto completo: 1 Índice: WPRIM Asunto principal: Hiperacusia / Vómitos / Encéfalo / Arteria Carótida Interna / Incidencia / Angiografía por Resonancia Magnética / Progresión de la Enfermedad / Constricción Patológica / Fotofobia / Cefalea Tipo de estudio: Incidence_studies / Prognostic_studies Límite: Child / Female / Humans Idioma: En Revista: Journal of the Korean Child Neurology Society Año: 2014 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Hiperacusia / Vómitos / Encéfalo / Arteria Carótida Interna / Incidencia / Angiografía por Resonancia Magnética / Progresión de la Enfermedad / Constricción Patológica / Fotofobia / Cefalea Tipo de estudio: Incidence_studies / Prognostic_studies Límite: Child / Female / Humans Idioma: En Revista: Journal of the Korean Child Neurology Society Año: 2014 Tipo del documento: Article