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Desafíos en el diagnóstico de enfermedad de Creutzfeldt-Jakob: caso clínico / Creutzfeldt-Jakob disease: report of one case
Ramírez, Marcos; Gallardo, Andrés; Vidal, Aarón; Cornejo, Sebastián; Ramírez, Darío; Medinas, Danilo; Bustamante, Gonzalo; Pasquali, Renzo; Hetz, Claudio.
  • Ramírez, Marcos; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas Oriente. Santiago. CL
  • Gallardo, Andrés; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas Oriente. Santiago. CL
  • Vidal, Aarón; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas Oriente. Santiago. CL
  • Cornejo, Sebastián; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas Oriente. Santiago. CL
  • Ramírez, Darío; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas Oriente. Santiago. CL
  • Medinas, Danilo; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas Oriente. Santiago. CL
  • Bustamante, Gonzalo; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas Oriente. Santiago. CL
  • Pasquali, Renzo; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas Oriente. Santiago. CL
  • Hetz, Claudio; Universidad de Chile. Facultad de Medicina. Departamento de Ciencias Neurológicas Oriente. Santiago. CL
Rev. méd. Chile ; 144(6): 796-806, jun. 2016. ilus, tab
Article in Spanish | LILACS | ID: lil-793988
ABSTRACT
Creutzfeldt-Jakob disease has a higher incidence in Chile than in other countries. The post mortem pathological characterization of brain tissue is necessary to reach a definitive diagnosis. We report a 73 years old man with a history compatible with of a rapidly progressive dementia, in which the first electroencephalographic study showed a pattern consistent with non-convulsive status epilepticus. Besides discarding this diagnosis, it was necessary to rule out other causes of rapidly progressive dementia such as Hashimoto encephalopathy. Finally, the sustained clinical deterioration with no response to anticonvulsants and corticosteroids, the imaging studies, a serial electroencephalographic monitoring study and the detection of 14-3-3 protein in cerebrospinal fluid were the keys to achieve the diagnosis of the disease.
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Full text: Available Index: LILACS (Americas) Main subject: Creutzfeldt-Jakob Syndrome Type of study: Diagnostic study Limits: Aged / Humans / Male Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2016 Type: Article Affiliation country: Chile Institution/Affiliation country: Universidad de Chile/CL

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Full text: Available Index: LILACS (Americas) Main subject: Creutzfeldt-Jakob Syndrome Type of study: Diagnostic study Limits: Aged / Humans / Male Language: Spanish Journal: Rev. méd. Chile Journal subject: Medicine Year: 2016 Type: Article Affiliation country: Chile Institution/Affiliation country: Universidad de Chile/CL