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Generalized Polyspike Pattern in EEG Due to Aseptic Meningoencephalitis

Hobert, Markus A,Dargvainiene, Justina,Margraf, Nils G

Abstract

We report the electroencephalography (EEG) showing an intermittent generalized polyspike pattern in EEG due to an aseptic meningoencephalitis in a 71-year-old soporous patient. Initially, she presented with word-finding disturbances and later with generalized tonic-clonic seizures. The cerebrospinal fluid (CSF) showed pleocytosis of 99 leukocytes/μL (primarily neutrophils) and an increased protein level of 1240 mg/L (CSF/serum glucose ratio and lactate unremarkable). Pathogens and autoimmune antibodies in CSF were not found. Brain imaging was unremarkable. After antibiotic, antiviral and anticonvulsive therapy, the pattern in the EEG was no longer detectable. The patient was discharged to go home due to absence of any residues.

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Citation: Hobert, M.A.; Dargvainiene, J.; Margraf, N.G. Generalized Polyspike Pattern in EEG Due to Aseptic Meningoencephalitis. Diagnostics 2023,13, 2569. https://doi.org/ 10.3390/diagnostics13152569 Academic Editors: Ayman El-Baz and Frank Weber Received: 2 July 2023 Revised: 19 July 2023 Accepted: 20 July 2023 Published: 2 August 2023 Copyright: © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/). diagnostics Interesting Images Generalized Polyspike Pattern in EEG Due to Aseptic Meningoencephalitis Markus A. Hobert 1,* , Justina Dargvainiene 2and Nils G. Margraf 1 1Department of Neurology, Christian-Albrecht University of Kiel and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany; [email protected] 2Institute of Clinical Chemistry, Christian-Albrecht University of Kiel and University Medical Center Schleswig-Holstein, 24105 Kiel, Germany; [email protected] *Correspondence: [email protected] Abstract: We report the electroencephalography (EEG) showing an intermittent generalized polyspike pattern in EEG due to an aseptic meningoencephalitis in a 71-year-old soporous patient. Initially, she presented with word-finding disturbances and later with generalized tonic–clonic seizures. The cerebrospinal fluid (CSF) showed pleocytosis of 99 leukocytes/ µ L (primarily neutrophils) and an increased protein level of 1240 mg/L (CSF/serum glucose ratio and lactate unremarkable). Pathogens and autoimmune antibodies in CSF were not found. Brain imaging was unremarkable. After antibiotic, antiviral and anticonvulsive therapy, the pattern in the EEG was no longer detectable. The patient was discharged to go home due to absence of any residues. Keywords: polyspike; aseptic meningoencephalitis; electroencephalogram 1 Figure 1. This electroencephalography (EEG) (10–20 system, sequential montage, sensitivity: 10 µ V/mm, high frequency filters: 70 Hz, time base: 15 mm/sec) showing an intermittent generalized polyspike pattern was found in a 71-year-old soporous patient due to an aseptic meningoencephalitis. Polyspikes ( A ) were followed by delta waves ( B ). Initially, the patient presented with word-finding disturbances and later with generalized tonic–clonic seizures. The cerebrospinal fluid (CSF) showed pleocytosis of 99 leukocytes/ µ L (primarily neutrophils) and an increased protein level of 1240 mg/L (CSF/serum glucose ratio and lactate unremarkable, identical oligoclonal bands in serum and liquor). Pathogens (Escherichia coli, Haemophilus influenzae, Listeria monocytogenes, Neisseria meningitidis, Streptococcus agalactiae, Streptococcus pneumoniae, Cytomegalovirus, Enterovirus, Herpes simplex virus 1, Herpes simplex virus 2, Varicella zoster virus, Cytomegalovirus, Human herpesvirus 6, Diagnostics 2023,13, 2569. https://doi.org/10.3390/diagnostics13152569 https://www.mdpi.com/journal/diagnostics Diagnostics 2023,13, 2569 2 of 3 Human parechovirus, Cryptococcus neoformans/gattii, Tick Borne Encephalitis virus and Borrelia burgdorferi) and autoimmune antibodies (antibodies against amphiphysin, contactin-associated protein-2 [CASPR 2], collapsin response mediator protein 5 [CRMP-5], gamma-aminobutyric acid-b [GABA b] receptor, leucine-rich glioma inactivated 1 [LGI 1], Ma-proteins, N-methyl-D-aspartate [NMDA] receptor, dipeptidyl-peptidase-like protein 6 [DPPX], alpha-amino-3-hydroxy-5-methyl4-isoxazolepropionic acid [AMPA]-receptor, Hu, Yo, Ri, glutamic acid decarboxylase [GAD] and myelin oligodendrocyte glycoprotein [MOG]) were not found in CSF. Magnetic resonance imaging (MRI) of the brain with contrast agent was unremarkable. Therapy was conducted with levetiracetam (2 × 1 g/die), lacosamide (2 × 100 mg/die), ceftriaxone, ampicillin and acyclovir. After clinical improvement, the pattern in the EEG was no longer detectable. The CSF after 8 days was normalized (cell count 3 leukocytes/ µ L). The patient was discharged to go home due to absence of any residues. Ten months later, the patient was examined in the outpatient clinic. She reported that no seizures occurred. The EEG was normal with no epileptiform discharges. A polyspike pattern in EEG represents interictal epileptiform discharges. It has been found in different immunological and structural conditions. Among these are encephalitis with MOG-antibodies [ 1 ] and with anti-ganglioside antibodies [ 2 ] or Hashimoto encephalopathy [ 3 ]. In general, EEG changes were found in patients with inflammatory processes in the brain [ 4 ]. Slow waves, epileptiform discharges and electroencephalic seizures were common in herpes encephalitis [ 5 ]. In autoimmune encephalitis, generalized or focal slowing, epileptiform discharges and electroencephalographic seizures were found [ 6 ]. Up to 28% of patients with aseptic meningitis without seizures had generalized and focal slowing [ 7 ]. In the reported case, no pathogens or autoimmune antibodies were found. Brain MRI also showed no structural changes. However, considering the symptoms with reported and observed generalized tonic-clonic seizures [ 8 ], the clinical course with improvement after treatment initiation, and the absence of the polyspike pattern on EEG after treatment initiation, it is most likely that the polyspike pattern was associated with meningoencephalitis. Although the cause of the meningoencephalitis (i.e., aseptic) was not found in the case reported here, neurologists should be aware that a polyspike pattern in EEG may be associated with an inflammatory process in the brain. Therefore, appropriate diagnostics should be performed if a polyspike pattern is found in the EEG. Author Contributions: Conceptualization, M.A.H. and N.G.M.; investigation, M.A.H., J.D. and N.G.M.; writing—original draft preparation, M.A.H.; writing—review and editing, J.D. and N.G.M.; visualization, M.A.H. All authors have read and agreed to the published version of the manuscript. Funding: This research received no external funding. Institutional Review Board Statement: Not applicable. Informed Consent Statement: The patient provided written informed content for publication of this EEG recording and clinical information. Data Availability Statement: Not applicable. Conflicts of Interest: The authors declare no conflict of interest. References 1. Maturu, M.V.S.; Datla, A.V.; Maturu, P.; Talla, V.B.; Dalai, S. Unilateral Autoimmune Encephalitis: A Case Report on a Rare Manifestation of Myelin Oligodendrocyte Glycoprotein Antibody Disease. Cureus 2023,15, e34994. [CrossRef] [PubMed] 2. Daida, K.; Nishioka, K.; Takanashi, M.; Kobayashi, M.; Yoshikawa, K.; Kusunoki, S.; Yokoyama, K.; Hattori, N. New-onset refractory status epilepticus involving the limbic system, spinal cord, and peripheral nerves. Intern. Med. 2020 ,59, 267–270. [CrossRef] [PubMed] 3. Arya, R.; Anand, V.; Chansoria, M. Hashimoto encephalopathy presenting as progressive myoclonus epilepsy syndrome. Eur. J. Paediatr. Neurol. 2013,17, 102–104. [CrossRef] [PubMed] 4. Michael, B.D.; Solomon, T. Seizures and encephalitis: Clinical features, management, and potential pathophysiologic mechanisms. Epilepsia 2012,53, 63–71. [CrossRef] [PubMed] 5. Sellner, J.; Trinka, E. Seizures and epilepsy in herpes simplex virus encephalitis: Current concepts and future directions of pathogenesis and management. J. Neurol. 2012,259, 2019–2030. [CrossRef] [PubMed] 6. Patel, A.; Meng, Y.; Najjar, A.; Lado, F.; Najjar, S. Autoimmune Encephalitis: A Physician’s Guide to the Clinical Spectrum Diagnosis and Management. Brain Sci. 2022,12, 1130. [CrossRef] [PubMed] Diagnostics 2023,13, 2569 3 of 3 7. Pollak, L.; Klein, C.; Schiffer, J.; Flechter, S.; Rabey, J.M. Electroencephalographic abnormalities in aseptic meningitis and noninfectious headache. A comparative study. Headache 2001,41, 79–83. [CrossRef] [PubMed] 8. Fisher, R.S.; Cross, J.H.; French, J.A.; Higurashi, N.; Hirsch, E.; Jansen, F.E.; Lagae, L.; Moshé, S.L.; Peltola, J.; Roulet Perez, E.; et al. Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology. Epilepsia 2017,58, 522–530. 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