Karatas Hulya, Dericioglu Nese, Kursun Oguzhan, Saygi Serap
Hacettepe University Hospitals, Department of Neurology, 06100 Sihhiye, Ankara, Turkey.
Clin EEG Neurosci. 2007 Oct;38(4):203-6. doi: 10.1177/155005940703800404.
Creutzfeldt-Jakob disease is the most common disorder among the very rare human transmissible subacute spongiform encephalopathies. Sporadic, familial or iatrogenic forms of the disease can be seen. The common presentations of the disease include rapidly progressive cognitive decline, behavioral changes, visual disturbances and cerebellar dysfunction. Hyperparathyroidism and toxicity of lithium and bismuth have been reported to induce similar symptoms and EEG findings, leading to a Creutzfeldt-Jakob like syndrome. We report a very rare case of Creutzfeldt-Jakob disease presenting with hyperparathyroidism and generalized tonic status epilepticus.
克雅氏病是极为罕见的人类可传播性亚急性海绵状脑病中最常见的疾病。可出现散发性、家族性或医源性形式的该疾病。该疾病的常见表现包括快速进展的认知衰退、行为改变、视觉障碍和小脑功能障碍。据报道,甲状旁腺功能亢进以及锂和铋中毒可诱发类似症状和脑电图表现,导致克雅氏病样综合征。我们报告了一例极为罕见的克雅氏病病例,其表现为甲状旁腺功能亢进和全身性强直癫痫持续状态。