Hashimoto's encephalopathy with clinical features similar to those of Creutzfeldt-Jakob disease.

نویسندگان

  • Ana Cláudia Rodrigues de Cerqueira
  • José Marcelo Ferreira Bezerra
  • Gérson Canedo de Magalhães
  • Márcia Rozenthal
  • Antônio Egídio Nardi
چکیده

Pedro Ernesto University Hospital of the University of the State of Rio de Janeiro, Rio de Janeiro RJ, Brazil (HUPE/UERJ): Neurology Service; Institute of Psychiatry at the Federal University of Rio de Janeiro, Rio de Janeiro RJ, Brazil (IPUB/UFRJ); Federal University of the State of Rio de Janeiro, Rio de Janeiro RJ, Brazil (Uni-Rio); Probative training student for Master’s Degree in Psychiatry; Associate Professor; Full Professor.

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منابع مشابه

Symptomatic aggravation after corticosteroid pulse therapy in definite sporadic Creutzfeldt-Jakob disease with the feature of Hashimoto’s encephalopathy

BACKGROUND Creutzfeldt-Jakob disease and Hashimoto's encephalopathy often show similar clinical presentation. Among Creutzfeldt-Jakob disease mimics, Hashimoto's encephalopathy is particularly important as it is treatable with corticosteroids. Thus, in cases of middle-aged woman diagnosed with probable Creutzfeldt-Jakob disease and who exhibit high titers of antithyroid antibodies, corticostero...

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[Diagnosis and treatments of Hashimoto's encephalopathy].

Hashimoto's encephalopathy (HE), which is occasionally associated with chronic thyroiditis (Hashimoto's disease), presents with a variety of neurologic and neuropsychiatric features. We investigated the clinical features and treatments in 80 cases of HE with serum anti-NH(2)-terminal of α-enolase [anti-NAE] autoantibodies, a useful diagnostic marker of this disease. The acute encephalopathy for...

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Variant Creutzfeldt-Jakob disease.

Current evidence indicates that variant Creutzfeldt-Jakob disease is caused by the transmission of bovine spongiform encephalopathy to humans. The clinical and investigative features of variant CJD are relatively distinct from sporadic CJD and the neuropathological appearances are novel. The number of cases of vCJD in the UK may have peaked, but the total future number of cases of vCJD is uncer...

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Hashimoto's encephalitis as a differential diagnosis of Creutzfeldt-Jakob disease.

OBJECTIVES During an epidemiological study of Creutzfeldt-Jakob disease in Germany, Hashimoto's encephalitis was encountered as a differential diagnosis, which has not yet been described in this context. METHODS The symptoms and findings of seven patients who fulfilled the criteria for "possible" Creutzfeldt-Jakob disease are presented. RESULTS A Hashimoto's thyroiditis with antibodies agai...

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Creutzfeldt-Jacob Disease in an Iranian Patient Confirmed By Brain Autopsy

Creutzfeldt-Jacob disease is the most common form of prion diseases, which have become public health problems in the last two decades because of the high number of reported cases of mad cow disease in Great Britain and other countries. Creutzfeldt-Jacob disease is a fatal situation with known cardinal clinical features including progressive memory loss and myoclonic seizure disorder. In this re...

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عنوان ژورنال:
  • Arquivos de neuro-psiquiatria

دوره 66 4  شماره 

صفحات  -

تاریخ انتشار 2008