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Journal of Korean Medical Science ; : 965-968, 2012.
Artigo em Inglês | WPRIM | ID: wpr-56886

RESUMO

Mixed autonomic hyperactivity disorder (MAHD) among patients with acquired brain injury can be rare. A delayed diagnosis of MAHD might exacerbate the clinical outcome and increase healthcare expenses with unnecessary testing. However, MAHD is still an underrecognized and evolving disease entity. A 25-yr-old woman was admitted the clinic due to craniopharyngioma. After an extensive tumor resection, she complained of sustained fever, papillary contraction, hiccup, lacrimation, and sighing. An extensive evaluation of the sustained fever was conducted. Finally, the cause for MAHD was suspected, and the patient was successfully treated with bromocriptine for a month.


Assuntos
Adulto , Feminino , Humanos , Encéfalo/diagnóstico por imagem , Bromocriptina/uso terapêutico , Craniofaringioma/complicações , Febre/complicações , Antagonistas de Hormônios/uso terapêutico , Hipercinese/complicações , Imageamento por Ressonância Magnética , Procedimentos Neurocirúrgicos/efeitos adversos , Neoplasias Hipofisárias/complicações , Tomografia Computadorizada por Raios X
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