Literature DB >> 14744571

Creutzfeldt-Jakob disease and non-convulsive status epilepticus: a clinical and electroencephalographic follow-up study.

J L Fernández-Torre1, D M Solar, A Astudillo, R Cereceda, A Acebes, M T Calatayud.   

Abstract

OBJECTIVE: To describe the clinical and electroencephalographic findings from a confused elderly woman with Creutzfeldt-Jakob disease (CJD) that initially were compatible with the diagnosis of non-convulsive status epilepticus (NCSE). METHODS AND
RESULTS: A 75-year-old right-handed woman was admitted to our hospital because of confusion and alteration of mental status. The two first electroencephalograms (EEGs) showed continuous diffuse spikes, rhythmic sharp waves and sharp-and-slow wave complexes which were completely abolished after the administration of 10 mg of intravenous diazepam. Over the following days, the clinical state of the patient was unmodified despite aggressive antiepileptic therapy. A third EEG revealed pseudo-periodic negative or positive-negative slow waves localised in the right frontal region. Subsequently, two consecutive EEGs showed continuous periodic generalised bi-triphasic complexes at a rate of 1 Hz, compatible with the diagnosis of CJD. Finally, the patient died, and postmortem examination was diagnostic of the sporadic form of CJD.
CONCLUSIONS: Clinical and electroencephalographic features in the early stages of CJD may resemble NCSE. The administration of intravenous benzodiazepines and its clinical and electroencephalographic correlation, response to the antiepileptic therapy, and monitoring with serial EEG recordings may be helpful considerations in the differential diagnosis.

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Year:  2004        PMID: 14744571     DOI: 10.1016/j.clinph.2003.10.012

Source DB:  PubMed          Journal:  Clin Neurophysiol        ISSN: 1388-2457            Impact factor:   3.708


  5 in total

1.  Treating seizures in Creutzfeldt-Jakob disease.

Authors:  Marcus C Ng; M Brandon Westover; Andrew J Cole
Journal:  Epilepsy Behav Case Rep       Date:  2014-02-07

2.  Creutzfeldt-Jakob Disease Presenting as Nonconvulsive Status Epilepticus.

Authors:  Aleksei Rakitin; Riina Vibo; Vaiko Veikat; Anne Õunapuu; Aive Liigant; Sulev Haldre
Journal:  Case Rep Neurol Med       Date:  2018-11-04

3.  Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases.

Authors:  Simote T Foliaki; Benjamin Schwarz; Bradley R Groveman; Ryan O Walters; Natalia C Ferreira; Christina D Orrù; Anna Smith; Aleksandar Wood; Olivia M Schmit; Phoebe Freitag; Jue Yuan; Wenquan Zou; Catharine M Bosio; James A Carroll; Cathryn L Haigh
Journal:  Mol Brain       Date:  2021-10-11       Impact factor: 4.041

4.  Sporadic Creutzfeldt-Jakob Disease With Status Epilepticus: Molecular Mechanisms and a Scoping Review of the Literature.

Authors:  Bahadar S Srichawla
Journal:  Cureus       Date:  2022-08-31

5.  Focal sharp waves are a specific early-stage marker of the MM2-cortical form of sporadic Creutzfeldt-Jakob disease.

Authors:  Taiki Matsubayashi; Miho Akaza; Yuichi Hayashi; Tsuyoshi Hamaguchi; Masahito Yamada; Takayoshi Shimohata; Takanori Yokota; Nobuo Sanjo
Journal:  Prion       Date:  2020-12       Impact factor: 3.931

  5 in total

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