Autoimmune and limbic encephalitis: case series with some atypical variables in clinical practice
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F22%3A00075987" target="_blank" >RIV/65269705:_____/22:00075987 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14110/22:00125087
Result on the web
<a href="https://link.springer.com/article/10.1007/s10072-021-05563-x" target="_blank" >https://link.springer.com/article/10.1007/s10072-021-05563-x</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s10072-021-05563-x" target="_blank" >10.1007/s10072-021-05563-x</a>
Alternative languages
Result language
angličtina
Original language name
Autoimmune and limbic encephalitis: case series with some atypical variables in clinical practice
Original language description
Autoimmune and limbic encephalitides are still rare diseases characterized by rapid diagnostics and treatment development in recent years. The incidence of anti-N-methyl-D- aspartate receptor [NMDAR] encephalitis is about 1.5 per million person per year, and the incidence of paraneoplastic neurological syndromes [PNS] including limbic encephalitis [LE] is about 1.22 per 100 000 person per year (Vogrig et al. J Neurol 267:26-35, 1; Dalmau et al. Ann Neurol 61:25-36, 2). The diagnostic criteria of anti-NMDAR encephalitis are already well established (Zuliani et al. Neurol Sci 40:2017-2030, 10). We provide immunological and clinical characteristics of anti-NMDAR encephalitis case series emphasizing unusual association with colon tumour in one case and complete recovery in two cases. Then we report two cases of onconeural and cell surface antibody negative limbic encephalitis [LE] associated with tumours, seizures, cognitive and behavioural changes resulting in severe cerebellar syndrome and fatal outcome. The clinical characteristics and results of selected paraclinical examinations as electroencephalography [EEG], magnetic resonance imaging [MRI] and cerebrospinal fluid [CSF] analysis are reviewed.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30210 - Clinical neurology
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Neurological Sciences
ISSN
1590-1874
e-ISSN
1590-3478
Volume of the periodical
43
Issue of the periodical within the volume
1
Country of publishing house
IT - ITALY
Number of pages
4
Pages from-to
687-690
UT code for WoS article
000687902800001
EID of the result in the Scopus database
2-s2.0-85113315851