J Korean Neurol Assoc.  2004 Aug;22(4):406-409.

A Case of Probable Creutzfeldt-Jakob Disease with Coexistence of the Features of Hashimoto Encephalopathy

Affiliations
  • 1Department of Neurology, Yonsei University College of Medicine, Seoul, Korea. scpark@yumc.yonsei.ac.kr
  • 2Department of Diagnostic Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea.
  • 3Ilsong Institute of Life Science, Hallym University, Korea.

Abstract

Hashimoto encephalopathy shares common clinical features with Creutzfeldt-Jakob disease and must be regarded as a differential diagnosis because of its good prognosis. We report a case of Hashimoto encephalopathy, which had not been recognized before the diagnosis of Creutzfeldt-Jakob disease. The electroclinical findings were compatible with probable Creutzfeldt-Jakob disease and coexistence of Hashimoto thyroiditis was supported by high titers of anti-thyroid microsomal antibody and cytopathologic findings. Hashimoto encephalopathy was not improved, which was most likely due to the coexistence of Creutzfeldt-Jakob disease.

Keyword

Hashimoto encephalopathy; Creutzfeldt-Jakob disease; Differential diagnosis

MeSH Terms

Creutzfeldt-Jakob Syndrome*
Diagnosis
Diagnosis, Differential
Hashimoto Disease
Prognosis
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