Creutzfeldt-Jakob disease. A survey of 14 patients

• Published in: Arquivos de neuro-psiquiatria 1996-12, Vol.54 (4), p.577-583
• Main Authors: Marchiori, P E, Yasuda, N, Azevedo, H C, Orfão, M, Callegaro, D, Yamamoto, F I, Scaff, M
• Format: Article
• Language: English
• Subjects: Adult; Aged; Creutzfeldt-Jakob Syndrome - diagnosis; Disease Progression; Female; Humans; Male; Middle Aged; NEUROSCIENCES; PSYCHIATRY
• ISSN: 0004-282X; 1678-4227; 0004-282X
• DOI: 10.1590/s0004-282x1996000400005

Creutzfeldt-Jakob disease (CJD) is a transmissible disease of the nervous system causatively related to the presence of an abnormal prion protein, with dementia, myoclonic jerks, and periodic EEG activity. Fourteen patients (7 females and 7 males) ranging from 26 to 76 years of age (median 59 years) were evaluated between 1974 and 1995 at the Neurologic Clinic of São Paulo University School of Medicine. The average duration of the disease was 12 months (3.5-34 months). Early clinical findings were: behaviour changes in 7 patients, dementia in 4, visual disturbances in 4, vertigo in 2, tremor in 9, and dystonia in one. Advanced symptoms were dementia and myoclonus in all patients. Pyramidal tract dysfunction was found in 6, cerebellar ataxia in 2, seizures in 3, nystagmus and vertigo in 4, and peripheral nervous system involvement in 2. Atypical clinical forms were found in 5 patients. Periodic EEG activity was found in 10 patients. Cerebrospinal fluid evaluation showed pleocytosis in 1 patient, higher protein content in 2, and higher gamma globulin level in 2. In 10 patients anatomopathological evidence in the central nervous system confirmed the clinical diagnosis by presenting with status spongiosus. All except one patient presented with the sporadic form of the disease.