Factors underlying the development of chronic temporal lobe epilepsy in autoimmune encephalitis
Limbic encephalitis (LE) is an autoimmune condition characterized by amnestic syndrome, psychiatric features and seizures. Early diagnosis and prompt treatment are crucial to avoid long-term sequelae, including psycho-cognitive deficits and persisting seizures. The aim of our study was to analyze th...
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Published in | Journal of the neurological sciences Vol. 396; pp. 102 - 107 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
15.01.2019
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ISSN | 0022-510X 1878-5883 1878-5883 |
DOI | 10.1016/j.jns.2018.10.026 |
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Abstract | Limbic encephalitis (LE) is an autoimmune condition characterized by amnestic syndrome, psychiatric features and seizures. Early diagnosis and prompt treatment are crucial to avoid long-term sequelae, including psycho-cognitive deficits and persisting seizures.
The aim of our study was to analyze the characteristics of 33 LE patients in order to identify possible prognostic factors associated with the development of chronic epilepsy.
This is a retrospective cohort study including adult patients diagnosed with LE in the period 2010–2017 and followed up for ≥12 months. Demographics, seizure semiology, EEG pattern, MRI features, CSF/serum findings were reviewed.
All 33 LE patients (19 M/14F, mean age 61.2 years) presented seizures. Thirty subjects had memory deficits; 22 presented behavioural/mood disorders. Serum and/or CSF auto-antibodies were detected in 12 patients. In 31 subjects brain MRI at onset showed typical alterations involving temporal lobes. All patients received immunotherapy. At follow-up, 13/33 had developed chronic epilepsy; predisposing factors included delay in diagnosis (p = .009), low seizure frequency at onset (p = .02), absence of amnestic syndrome (p = .02) and absence/rarity of inter-ictal epileptic discharges on EEG (p = .06).
LE with paucisymptomatic electro-clinical presentation seemed to be associated to chronic epilepsy more than LE presenting with definite and severe “limbic syndrome”.
•LE is a potentially treatable, often overlooked, immune-mediated condition•In acute phase its clinical spectrum includes seizures and psycho-cognitive disorders•Chronic epilepsy with predominant temporal seizures can represent a long term sequela•Some specific factors are associated with the development of chronic epilepsy•These factors include diagnostic delay and mild/uncomplete phenotype at onset |
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AbstractList | Limbic encephalitis (LE) is an autoimmune condition characterized by amnestic syndrome, psychiatric features and seizures. Early diagnosis and prompt treatment are crucial to avoid long-term sequelae, including psycho-cognitive deficits and persisting seizures. The aim of our study was to analyze the characteristics of 33 LE patients in order to identify possible prognostic factors associated with the development of chronic epilepsy.PURPOSELimbic encephalitis (LE) is an autoimmune condition characterized by amnestic syndrome, psychiatric features and seizures. Early diagnosis and prompt treatment are crucial to avoid long-term sequelae, including psycho-cognitive deficits and persisting seizures. The aim of our study was to analyze the characteristics of 33 LE patients in order to identify possible prognostic factors associated with the development of chronic epilepsy.This is a retrospective cohort study including adult patients diagnosed with LE in the period 2010-2017 and followed up for ≥12 months. Demographics, seizure semiology, EEG pattern, MRI features, CSF/serum findings were reviewed.METHODSThis is a retrospective cohort study including adult patients diagnosed with LE in the period 2010-2017 and followed up for ≥12 months. Demographics, seizure semiology, EEG pattern, MRI features, CSF/serum findings were reviewed.All 33 LE patients (19 M/14F, mean age 61.2 years) presented seizures. Thirty subjects had memory deficits; 22 presented behavioural/mood disorders. Serum and/or CSF auto-antibodies were detected in 12 patients. In 31 subjects brain MRI at onset showed typical alterations involving temporal lobes. All patients received immunotherapy. At follow-up, 13/33 had developed chronic epilepsy; predisposing factors included delay in diagnosis (p = .009), low seizure frequency at onset (p = .02), absence of amnestic syndrome (p = .02) and absence/rarity of inter-ictal epileptic discharges on EEG (p = .06).RESULTSAll 33 LE patients (19 M/14F, mean age 61.2 years) presented seizures. Thirty subjects had memory deficits; 22 presented behavioural/mood disorders. Serum and/or CSF auto-antibodies were detected in 12 patients. In 31 subjects brain MRI at onset showed typical alterations involving temporal lobes. All patients received immunotherapy. At follow-up, 13/33 had developed chronic epilepsy; predisposing factors included delay in diagnosis (p = .009), low seizure frequency at onset (p = .02), absence of amnestic syndrome (p = .02) and absence/rarity of inter-ictal epileptic discharges on EEG (p = .06).LE with paucisymptomatic electro-clinical presentation seemed to be associated to chronic epilepsy more than LE presenting with definite and severe "limbic syndrome".CONCLUSIONSLE with paucisymptomatic electro-clinical presentation seemed to be associated to chronic epilepsy more than LE presenting with definite and severe "limbic syndrome". Limbic encephalitis (LE) is an autoimmune condition characterized by amnestic syndrome, psychiatric features and seizures. Early diagnosis and prompt treatment are crucial to avoid long-term sequelae, including psycho-cognitive deficits and persisting seizures. The aim of our study was to analyze the characteristics of 33 LE patients in order to identify possible prognostic factors associated with the development of chronic epilepsy. This is a retrospective cohort study including adult patients diagnosed with LE in the period 2010–2017 and followed up for ≥12 months. Demographics, seizure semiology, EEG pattern, MRI features, CSF/serum findings were reviewed. All 33 LE patients (19 M/14F, mean age 61.2 years) presented seizures. Thirty subjects had memory deficits; 22 presented behavioural/mood disorders. Serum and/or CSF auto-antibodies were detected in 12 patients. In 31 subjects brain MRI at onset showed typical alterations involving temporal lobes. All patients received immunotherapy. At follow-up, 13/33 had developed chronic epilepsy; predisposing factors included delay in diagnosis (p = .009), low seizure frequency at onset (p = .02), absence of amnestic syndrome (p = .02) and absence/rarity of inter-ictal epileptic discharges on EEG (p = .06). LE with paucisymptomatic electro-clinical presentation seemed to be associated to chronic epilepsy more than LE presenting with definite and severe “limbic syndrome”. •LE is a potentially treatable, often overlooked, immune-mediated condition•In acute phase its clinical spectrum includes seizures and psycho-cognitive disorders•Chronic epilepsy with predominant temporal seizures can represent a long term sequela•Some specific factors are associated with the development of chronic epilepsy•These factors include diagnostic delay and mild/uncomplete phenotype at onset Limbic encephalitis (LE) is an autoimmune condition characterized by amnestic syndrome, psychiatric features and seizures. Early diagnosis and prompt treatment are crucial to avoid long-term sequelae, including psycho-cognitive deficits and persisting seizures. The aim of our study was to analyze the characteristics of 33 LE patients in order to identify possible prognostic factors associated with the development of chronic epilepsy. This is a retrospective cohort study including adult patients diagnosed with LE in the period 2010-2017 and followed up for ≥12 months. Demographics, seizure semiology, EEG pattern, MRI features, CSF/serum findings were reviewed. All 33 LE patients (19 M/14F, mean age 61.2 years) presented seizures. Thirty subjects had memory deficits; 22 presented behavioural/mood disorders. Serum and/or CSF auto-antibodies were detected in 12 patients. In 31 subjects brain MRI at onset showed typical alterations involving temporal lobes. All patients received immunotherapy. At follow-up, 13/33 had developed chronic epilepsy; predisposing factors included delay in diagnosis (p = .009), low seizure frequency at onset (p = .02), absence of amnestic syndrome (p = .02) and absence/rarity of inter-ictal epileptic discharges on EEG (p = .06). LE with paucisymptomatic electro-clinical presentation seemed to be associated to chronic epilepsy more than LE presenting with definite and severe "limbic syndrome". AbstractPurposeLimbic encephalitis (LE) is an autoimmune condition characterized by amnestic syndrome, psychiatric features and seizures. Early diagnosis and prompt treatment are crucial to avoid long-term sequelae, including psycho-cognitive deficits and persisting seizures. The aim of our study was to analyze the characteristics of 33 LE patients in order to identify possible prognostic factors associated with the development of chronic epilepsy. MethodsThis is a retrospective cohort study including adult patients diagnosed with LE in the period 2010–2017 and followed up for ≥12 months. Demographics, seizure semiology, EEG pattern, MRI features, CSF/serum findings were reviewed. ResultsAll 33 LE patients (19 M/14F, mean age 61.2 years) presented seizures. Thirty subjects had memory deficits; 22 presented behavioural/mood disorders. Serum and/or CSF auto-antibodies were detected in 12 patients. In 31 subjects brain MRI at onset showed typical alterations involving temporal lobes. All patients received immunotherapy. At follow-up, 13/33 had developed chronic epilepsy; predisposing factors included delay in diagnosis ( p = .009), low seizure frequency at onset ( p = .02), absence of amnestic syndrome (p = .02) and absence/rarity of inter-ictal epileptic discharges on EEG ( p = .06). ConclusionsLE with paucisymptomatic electro-clinical presentation seemed to be associated to chronic epilepsy more than LE presenting with definite and severe “limbic syndrome”. |
Author | Basili, Luca Manfredi Fattouch, Jinane Di Gennaro, Giancarlo Di Bonaventura, Carlo Quarato, Pierpaolo Viganò, Alessandro Casciato, Sara De Risi, Marco Manfredi, Mario Fanella, Martina Avorio, Federica Albini, Mariarita Cerulli Irelli, Emanuele Morano, Alessandra Grammaldo, Liliana G. Mascia, Addolorata Giallonardo, Anna Teresa D'Aniello, Alfredo |
Author_xml | – sequence: 1 givenname: Sara surname: Casciato fullname: Casciato, Sara organization: IRCCS “NEUROMED”, Pozzilli (IS), Italy – sequence: 2 givenname: Alessandra surname: Morano fullname: Morano, Alessandra organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy – sequence: 3 givenname: Jinane surname: Fattouch fullname: Fattouch, Jinane organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy – sequence: 4 givenname: Martina surname: Fanella fullname: Fanella, Martina organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy – sequence: 5 givenname: Federica surname: Avorio fullname: Avorio, Federica organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy – sequence: 6 givenname: Mariarita surname: Albini fullname: Albini, Mariarita organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy – sequence: 7 givenname: Luca Manfredi surname: Basili fullname: Basili, Luca Manfredi organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy – sequence: 8 givenname: Emanuele surname: Cerulli Irelli fullname: Cerulli Irelli, Emanuele organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy – sequence: 9 givenname: Alessandro surname: Viganò fullname: Viganò, Alessandro organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy – sequence: 10 givenname: Marco surname: De Risi fullname: De Risi, Marco organization: IRCCS “NEUROMED”, Pozzilli (IS), Italy – sequence: 11 givenname: Liliana G. surname: Grammaldo fullname: Grammaldo, Liliana G. organization: IRCCS “NEUROMED”, Pozzilli (IS), Italy – sequence: 12 givenname: Alfredo surname: D'Aniello fullname: D'Aniello, Alfredo organization: IRCCS “NEUROMED”, Pozzilli (IS), Italy – sequence: 13 givenname: Addolorata surname: Mascia fullname: Mascia, Addolorata organization: IRCCS “NEUROMED”, Pozzilli (IS), Italy – sequence: 14 givenname: Mario surname: Manfredi fullname: Manfredi, Mario organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy – sequence: 15 givenname: Pierpaolo surname: Quarato fullname: Quarato, Pierpaolo organization: IRCCS “NEUROMED”, Pozzilli (IS), Italy – sequence: 16 givenname: Anna Teresa surname: Giallonardo fullname: Giallonardo, Anna Teresa organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy – sequence: 17 givenname: Giancarlo surname: Di Gennaro fullname: Di Gennaro, Giancarlo organization: IRCCS “NEUROMED”, Pozzilli (IS), Italy – sequence: 18 givenname: Carlo surname: Di Bonaventura fullname: Di Bonaventura, Carlo email: c_dibonaventura@yahoo.it organization: Epilepsy Unit, Department of Neurosciences/Mental Health, “Sapienza” University, Rome, Italy |
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Keywords | Autoimmune encephalopathies Chronic focal epilepsy Limbic encephalitis Seizures |
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Snippet | Limbic encephalitis (LE) is an autoimmune condition characterized by amnestic syndrome, psychiatric features and seizures. Early diagnosis and prompt treatment... AbstractPurposeLimbic encephalitis (LE) is an autoimmune condition characterized by amnestic syndrome, psychiatric features and seizures. Early diagnosis and... |
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SubjectTerms | Adolescent Adult Aged Aged, 80 and over Autoimmune encephalopathies Chronic focal epilepsy Cognition Disorders - etiology Cohort Studies Disease Progression Electroencephalography Encephalitis - complications Encephalitis - psychology Encephalitis - therapy Epilepsy, Temporal Lobe - diagnostic imaging Epilepsy, Temporal Lobe - etiology Female Hashimoto Disease - complications Hashimoto Disease - psychology Hashimoto Disease - therapy Humans Immunotherapy - methods Limbic encephalitis Magnetic Resonance Imaging Male Middle Aged Neurology Seizures Young Adult |
Title | Factors underlying the development of chronic temporal lobe epilepsy in autoimmune encephalitis |
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