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1.
Front Neurol ; 12: 611597, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-33767656

RESUMO

Background: In our previous single-center study of autoimmune encephalitis (AE) related autoantibody test results we found positivity in 60 patients out of 1,034 with suspected AE from 2012 through 2018 as part of a Hungarian nationwide program. In our current multicenter retrospective study, we analyzed the clinical characteristics and outcome of AE patients with positive neuronal cell surface autoantibody test results. Methods: A standard online questionnaire was used to collect demographic and clinical characteristics, laboratory and imaging data, therapy and prognosis of 30 definitive AE patients in four major clinical centers of the region. Results: In our study, 19 patients were positive for anti-NMDAR (63%), 6 patients (20%) for anti-LGI1, 3 patients for anti-GABABR (10%) and 3 patients for anti-Caspr2 (10%) autoantibodies. Most common prodromal symptoms were fever or flu-like symptoms (10/30, 33%). Main clinical features included psychiatric symptoms (83%), epileptic seizures (73%) and memory loss (50%). 19 patients (63%) presented with signs of central nervous system (CNS) inflammation, which occurred more frequently in elder individuals (p = 0.024), although no significant differences were observed in sex, tumor association, time to diagnosis, prognosis and immunotherapy compared to AE patients without CNS inflammatory markers. Anti-NMDAR encephalitis patients were in more severe condition at the disease onset (p = 0.028), although no significant correlation between mRS score, age, sex and immunotherapy was found. 27% of patients (n = 8) with associated tumors had worse outcome (p = 0.045) than patients without tumor. In most cases, immunotherapy led to clinical improvement of AE patients (80%) who achieved a good outcome (mRS ≤ 2; median follow-up 33 months). Conclusion: Our study confirms previous publications describing characteristics of AE patients, however, differences were observed in anti-NMDAR encephalitis that showed no association with ovarian teratoma and occurred more frequently among young males. One-third of AE patients lacked signs of inflammation in both CSF and brain MRI, which emphasizes the importance of clinical symptoms and autoantibody testing in diagnostic workflow for early introduction of immunotherapy, which can lead to favorable outcome in AE patients.

2.
Ideggyogy Sz ; 73(11-12): 427-430, 2020 Nov 30.
Artigo em Húngaro | MEDLINE | ID: mdl-33264532

RESUMO

The clinical signs of SARS-CoV-2 infection has become more recognisable in recent times. In addition to common symptoms such as fever, cough, dyspnea, pneumonia and ageusia, less common complications can be identified, including many neurological manifestations. In this paper, we discuss three Covid-19 associated neurological disorders (Case 1: Covid-19 encephalitis, Case 2: Covid-19 organic headache, Case 3: SARS-CoV-2-infection and ischaemic stroke). We emphasize in our multiple case study that during the present pandemic, it is especially important for neurologists to be aware of the nervous system complications of the virus infection, thus saving unnecessary examinations and reducing the frequency of patients' contact with health care personnel.


Assuntos
Isquemia Encefálica/virologia , COVID-19 , Infecções por Coronavirus/diagnóstico , Cefaleia/virologia , Pneumonia Viral/diagnóstico , Acidente Vascular Cerebral/virologia , Isquemia Encefálica/complicações , Coronavirus , Infecções por Coronavirus/complicações , Encefalite , Cefaleia/complicações , Humanos , Doenças do Sistema Nervoso/complicações , Doenças do Sistema Nervoso/virologia , Pneumonia Viral/complicações , Acidente Vascular Cerebral/complicações
3.
Orv Hetil ; 158(42): 1681-1684, 2017 Oct.
Artigo em Húngaro | MEDLINE | ID: mdl-29037056

RESUMO

In a patient with marked symptoms of Huntington disease after the huntingtin testing, which gave normal result, a whole exome sequencing (WES) has been performed based on an international collaboration. A homozygous G>A nucleotid change in the exon 34 of the VPS13A gene has been detected with WES, a mutation resulting in a premature stop codon at the position 1301. This change is a known pathogenic mutation. The aim of this article is to draw attention on the importance of the WES in the diagnosis of rare neurological diseases without any specific symptoms. Orv Hetil. 2017; 158(42): 1681-1684.


Assuntos
Neuroacantocitose/diagnóstico , Proteínas de Transporte Vesicular/genética , Sequência de Bases , Humanos , Neuroacantocitose/genética , Reação em Cadeia da Polimerase , Análise de Sequência de DNA
4.
J Neurol Sci ; 376: 159-165, 2017 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-28431605

RESUMO

BACKGROUND: Chronic cognitive deficits are frequent in leucin-rich glioma-inactivated 1 protein (LGI1) encephalitis. We examined structural and metabolic brain abnormalities following LGI1 encephalitis and correlated findings with acute and follow-up clinical outcomes. METHODS: Nine patients underwent prospective multimodal 3 Tesla MRI 33.1±18months after disease onset, including automated volumetry, diffusion tensor imaging (DTI) and magnetic resonance spectroscopy (MRS). Data were compared to 9 age- and sex-matched healthy controls. RESULTS: Although extratemporal lesions were not present on MRI in the acute stage, tract-based spatial statistics analyses of DTI during follow-up showed widespread changes in the cerebral and cerebellar white matter (WM), most prominent in the anterior parts of the corona radiata, capsula interna and corpus callosum. MRS revealed lower glutamine/glutamate WM levels compared to controls. Higher cerebellar gray matter volume was associated with better function at disease onset (measured by the modified Rankin Scale), and higher putaminal volume was associated with better cognition by Addenbrooke's Cognitive Examination test at 23.4±7.6months. CONCLUSIONS: Poor clinical outcome following LGI1 encephalitis is associated with global brain atrophy and disintegration of white matter tracts. The pathological changes affect not only temporomesial structures but also frontal lobes and the cerebellum.


Assuntos
Doenças Autoimunes do Sistema Nervoso/diagnóstico por imagem , Encéfalo/diagnóstico por imagem , Imagem de Tensor de Difusão , Encefalite/diagnóstico por imagem , Imageamento por Ressonância Magnética , Espectroscopia de Ressonância Magnética , Doença Aguda , Atrofia , Doenças Autoimunes do Sistema Nervoso/tratamento farmacológico , Doenças Autoimunes do Sistema Nervoso/metabolismo , Encéfalo/metabolismo , Doença Crônica , Encefalite/tratamento farmacológico , Encefalite/imunologia , Feminino , Seguimentos , Humanos , Peptídeos e Proteínas de Sinalização Intracelular , Masculino , Pessoa de Meia-Idade , Imagem Multimodal , Tamanho do Órgão , Estudos Prospectivos , Proteínas/imunologia , Estudos Retrospectivos , Resultado do Tratamento
5.
Ideggyogy Sz ; 69(7-8): 281-287, 2016 Jul 30.
Artigo em Inglês | MEDLINE | ID: mdl-29465894

RESUMO

GABAB receptor (gamma-aminobutyric acid type B receptors - GABABR) encephalitis is a rare manifestation of autoimmune encephalitides. We report four cases - including the first two Hungarian patients - with some peculiar features. One patient developed subacute disorientation and almost complete loss of short-term memory, but no epilepsy. Without immunotherapy, his memory spontaneously improved up to mild cognitive impairment in six weeks. GABABR antibodies persisted in his serum, and 18 months later, FDG-PET detected abnormal mediastinal lymph nodes and small cell lung cancer (SCLC). Another patient had persistently decreased sodium content in the peripheral blood. In those three patients who died, CSF was abnormal, but CSF was not pathological in the patient, who spontaneously improved. Brain MRI indicated signal intensity changes in the medial temporal areas in three cases. SCLC was found in three patients. Only the patient, who spontaneously improved, survived for more than 24 months. In summary, our cases show that (i) GABABR encephalitis may develop without epilepsy; (ii) the severe short-term memory loss can spontaneously improve; (iii) persistent hyponatremia can be present in the blood; (iv) the patient with benign course without epilepsy and CSF abnormality survived; (v) spontaneously remitting encephalitis can precede SCLC by 1.5 year, which emphasizes that repeated search for cancer is of paramount importance even in cases with spontaneous improvement.


Assuntos
Encefalite Límbica/imunologia , Encefalite Límbica/patologia , Receptores de GABA-B/imunologia , Idoso , Idoso de 80 Anos ou mais , Autoanticorpos/imunologia , Autoantígenos/imunologia , Humanos , Masculino , Pessoa de Meia-Idade
6.
Ideggyogy Sz ; 68(7-8): 252-7, 2015 Jul 30.
Artigo em Húngaro | MEDLINE | ID: mdl-26380419

RESUMO

AIM OF THE STUDY: In the present study, we report procedural and mid-term functional outcome data on the first 50 neurointerventional treatments of acute ischemic stroke in the Kaposi Mór County Hospital, Kaposvár, Hungary. MATERIALS AND METHODS: Endovascular recanalization of occluded large cervical and intracranial arteries was performed following an unsuccessful intravenous lysis or when intravenous lysis was contraindicated. A control cohort was retrospectively formed by analyzing data of 16 patients who has been unsuccesfully treated with iv. lysis before neurointervention was available in our hospital. RESULTS AND CONCLUSION: Recanalization rate was 84% and major complication rate was 2% in the neurointerventional group. Mid-term good functional outcome, defined as mRS 0-2, was achieved in 44% in the neurointerventional and in 13% in the intravenous lysis group, after 11.5 and 39.7 months follow-up period, respectively. Subgroup analysis revealed patient age as the strongest predictive factor of good functional outcome. Our data shows that neurointerventional treatment of acute ischemic stroke gives substantially improved functional outcome, in accordance with the results of the recently published international randomized trials.


Assuntos
Isquemia Encefálica/complicações , Artérias Cerebrais/cirurgia , Revascularização Cerebral/métodos , Procedimentos Endovasculares , Acidente Vascular Cerebral/etiologia , Acidente Vascular Cerebral/cirurgia , Adulto , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Isquemia Encefálica/diagnóstico por imagem , Angiografia Cerebral , Artérias Cerebrais/diagnóstico por imagem , Artérias Cerebrais/patologia , Constrição Patológica/cirurgia , Feminino , Seguimentos , Humanos , Hungria , Masculino , Pessoa de Meia-Idade , Procedimentos Neurocirúrgicos/métodos , Valor Preditivo dos Testes , Estudos Retrospectivos , Fatores de Risco , Acidente Vascular Cerebral/diagnóstico por imagem , Acidente Vascular Cerebral/fisiopatologia , Terapia Trombolítica , Tempo para o Tratamento , Tomografia Computadorizada por Raios X , Falha de Tratamento , Resultado do Tratamento
7.
Ideggyogy Sz ; 68(7-8): 279-85, 2015 Jul 30.
Artigo em Húngaro | MEDLINE | ID: mdl-26380423

RESUMO

In the recent years, it has been increasingly recognised that in a group of limbic encephalitis antibodies are directed against the scaffolding protein LGI1 (Leucine-rich glioma inactivated 1), which is part of the voltage gated potassium channel (VGKC) complex on neural synapses. Patients present with seizures and subacute history of neuropsychiatric symptoms, including psychosis and changes in memory, cognition, behaviour. Faciobrachial dystonic seizures can be observed, which are highly characteristic for LGI1 encephalitis. MRI shows medial temporal abnormalities in more than half of the cases. CSF evaluation is usually normal. Hyponatremia is frequently associated and may confuse the initial diagnosis. Early recognition and prompt initiation of immunotherapies are of great importance. The clinical improvements often correlate with the antibody levels. We present the case of a 64-year old man, who responded quickly to plasma exchange and major improvement was noted within few weeks.


Assuntos
Autoanticorpos/sangue , Encefalite Límbica/diagnóstico , Encefalite Límbica/terapia , Troca Plasmática , Proteínas/imunologia , Cognição , Diagnóstico Diferencial , Diagnóstico Precoce , Humanos , Hungria , Peptídeos e Proteínas de Sinalização Intracelular , Encefalite Límbica/complicações , Encefalite Límbica/metabolismo , Encefalite Límbica/psicologia , Imageamento por Ressonância Magnética , Masculino , Memória , Pessoa de Meia-Idade , Canais de Potássio de Abertura Dependente da Tensão da Membrana/metabolismo , Proteínas/metabolismo , Comportamento Social , Lobo Temporal/metabolismo , Lobo Temporal/patologia
8.
J Neurol Sci ; 343(1-2): 198-202, 2014 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-24928080

RESUMO

Antibodies against LGI1 (leucin-rich glioma-inactivated 1 protein) are associated with limbic encephalitis (LE), which is characterized by a favorable outcome following immunotherapy. Here, we present two cases, where antibodies against LGI1 were detected in the sera 36 and 53 months after acute LE, respectively, and none of the patients received immunotherapy. LE showed characteristics of LGI1 encephalitis in both cases, including low sodium content in the sera; disorientation, hallucination, short-term memory loss; and epileptic seizures. One patient had faciobrachial tonic seizures. MRI indicated bilateral inflammation of the hippocampus in one case. We reviewed longitudinal clinical and MRI data covering 53 and 36 months after LE without immunotherapy, respectively. Both patients became seizure-free and spontaneously recovered with mild/moderate cognitive impairment. No relapses have been observed. Follow-up brain MRI indicated early hippocampal sclerosis and global brain atrophy in one case characterized by more pronounced cognitive deficit. Memory and verbal fluency were affected most during the natural course of LGI1 encephalitis. LGI1 encephalitis had a monophasic course and spontaneously improved, suggesting that a relatively benign natural course may contribute to the favorable outcome observed after immunotherapy. Our data also indicate that LGI1 antibodies can be present in the sera without clinical disease activity.


Assuntos
Anticorpos/sangue , Encefalite Límbica , Proteínas/imunologia , Encéfalo/patologia , Humanos , Peptídeos e Proteínas de Sinalização Intracelular , Encefalite Límbica/sangue , Encefalite Límbica/patologia , Encefalite Límbica/terapia , Estudos Longitudinais , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Fatores de Tempo
9.
Orv Hetil ; 148(16): 749-52, 2007 Apr 22.
Artigo em Húngaro | MEDLINE | ID: mdl-17437952

RESUMO

Intravascular lymphomatosis is a rare systemic disease characterized by proliferation of malignant B or rarely T lymphocytes. Skin and the brain are predominantly affected. We describe a patient presenting with focal neurological signs and progressive dementia. Cerebral neuroimaging findings were nonspecific. Postmortem examination revealed intravascular proliferation of atypical mononuclear cells in the lumens of small vessels in all organs. The authors conclude that diagnosis requires a high index of suspicion and pathological examination of the affected organs, but is rarely made ante mortem.


Assuntos
Neoplasias das Glândulas Suprarrenais/diagnóstico , Neoplasias Encefálicas/diagnóstico , Linfoma não Hodgkin/diagnóstico , Neoplasias Meníngeas/diagnóstico , Neoplasias Vasculares/diagnóstico , Neoplasias das Glândulas Suprarrenais/patologia , Glândulas Suprarrenais/irrigação sanguínea , Linfócitos B/patologia , Biópsia , Neoplasias Encefálicas/complicações , Neoplasias Encefálicas/patologia , Confusão/etiologia , Diagnóstico Diferencial , Progressão da Doença , Evolução Fatal , Feminino , Humanos , Linfoma não Hodgkin/complicações , Linfoma não Hodgkin/patologia , Neoplasias Meníngeas/complicações , Neoplasias Meníngeas/patologia , Pessoa de Meia-Idade , Doenças Raras/diagnóstico , Neoplasias Vasculares/complicações , Neoplasias Vasculares/patologia
10.
CNS Drugs ; 18(3): 165-72, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-14871160

RESUMO

INTRODUCTION AND OBJECTIVE: Haemorrheological parameters and endothelial function are known to be altered in vascular diseases, including stroke. Treatment with HMG-CoA reductase inhibitors ('statins') improves cerebrovascular (and cardiovascular) morbidity and mortality in patients with atherosclerosis; the beneficial effects may involve lipid-independent mechanisms. The aim of this study was to assess the short-term effect of low-dose atorvastatin on haemorrheological parameters, platelet aggregation and endothelial dysfunction in patients with chronic cerebrovascular disease and hyperlipidaemia. PATIENTS AND METHODS: Twenty-seven patients (mean age 61 +/- 8 years) with chronic cerebrovascular disease and hyperlipidaemia were included in the study. Serum lipid levels, haemorrheological parameters (haematocrit, plasma fibrinogen levels, plasma and whole blood viscosity [WBV] and red blood cell [RBC] aggregation and deformability) and platelet aggregation were assessed at baseline and after 1 and 3 months of treatment with atorvastatin (Sortis) 10 mg/day. von Willebrand factor (vWF) activity (a measure of endothelial function) was measured at baseline and after 1 month of treatment. Adverse events were recorded at each visit. Physical examinations, haematological assessments and serum and urine chemistry assays were performed during the study. RESULTS: Plasma total cholesterol levels were reduced by a mean of 27% compared with baseline after both 1 and 3 months of treatment (p < 0.001). Low density lipoprotein-cholesterol levels were reduced by a mean of 40% and 38% (p < 0.001), respectively, after 1 and 3 months of treatment, compared with baseline values. Triglyceride levels decreased by 20% at 1 month and by 10% after 3 months (p < 0.001). Atorvastatin significantly improved WBV after 3 months of treatment and RBC deformability after 1 month and 3 months of treatment (p < 0.05). Collagen-induced platelet aggregation was significantly decreased at 1 (p < 0.05) and 3 months (p < 0.001) compared with baseline values, despite unaltered antiplatelet therapy. vWF activity was also improved significantly (p < 0.05) after 1 month of treatment. CONCLUSIONS: Our findings show that the beneficial effects of atorvastatin are complex. Besides lipid lowering, atorvastatin can improve haemorrheological parameters, platelet aggregation and endothelial dysfunction after short-term and low-dose therapy. Whether such early laboratory changes translate into clinical utility for secondary stroke prevention awaits the results of endpoint trials.


Assuntos
Hemorragia Cerebral/tratamento farmacológico , Transtornos Cerebrovasculares/tratamento farmacológico , Ácidos Heptanoicos/administração & dosagem , Hiperlipidemias/tratamento farmacológico , Agregação Plaquetária/efeitos dos fármacos , Pirróis/administração & dosagem , Idoso , Atorvastatina , Hemorragia Cerebral/sangue , Transtornos Cerebrovasculares/sangue , Transtornos Cerebrovasculares/complicações , Endotélio Vascular/efeitos dos fármacos , Endotélio Vascular/fisiologia , Feminino , Humanos , Hiperlipidemias/sangue , Hiperlipidemias/complicações , Masculino , Pessoa de Meia-Idade , Agregação Plaquetária/fisiologia , Fatores de Tempo
11.
Orv Hetil ; 144(20): 973-8, 2003 May 18.
Artigo em Húngaro | MEDLINE | ID: mdl-12830727

RESUMO

INTRODUCTION: Data collected from large number of multicenter, randomized trials in acute and chronic stroke patients provide evidence, that incidence and high mortality of cerebrovascular disorders can be decreased mainly by prevention and that the effectiveness of acute stroke treatment is limited. The terminology of "chronic cerebrovascular diseases" involves many pathologic entities and often atypical clinical symptoms refer to the focal or global hypoperfusion of the brain. However, hemorheological disturbances seem to be important factors of the complex pathomechanism. Vinpocetine has successfully been used in the treatment of cerebrovascular diseases, the part of the mechanism of action are the favourable rheological effects demonstrated after oral administration in more previous studies. AIMS AND METHODS: In this study the hemorheological changes after administration of small (30 mg/day) and high dose (increased to 70 mg/day) intravenous vinpocetine for 7 days in 30 patients in chronic phase of ischemic cerebrovascular disease were investigated. RESULTS: High dose parenteral vinpocetine treatment significantly (p < 0.05-0.005) decreased the hematocrit, the whole blood and plasma viscosity and red blood cell aggregation compared to the values before the treatment. Only red blood cell aggregation was improved significantly (p < 0.05) by small dose treatment. CONCLUSION: This study and other hemorheological studies in cerebrovascular patients demonstrated persistent rheological abnormalities despite the preventive therapy. The beneficial rheological effect of high dose parenteral vinpocetine indicates the use of this drug in the treatment of chronic cerebrovascular diseases.


Assuntos
Isquemia Encefálica/tratamento farmacológico , Isquemia Encefálica/fisiopatologia , Hemorreologia/efeitos dos fármacos , Alcaloides de Vinca/farmacologia , Idoso , Anti-Hipertensivos/farmacologia , Viscosidade Sanguínea/efeitos dos fármacos , Doença Crônica , Esquema de Medicação , Agregação Eritrocítica/efeitos dos fármacos , Feminino , Hematócrito , Humanos , Infusões Intravenosas , Masculino , Pessoa de Meia-Idade , Resultado do Tratamento , Vasodilatadores/farmacologia , Alcaloides de Vinca/administração & dosagem
12.
Orv Hetil ; 144(22): 1085-90, 2003 Jun 01.
Artigo em Húngaro | MEDLINE | ID: mdl-12847818

RESUMO

INTRODUCTION: Hemorheological factors are of significance in the determination of flow characteristics of blood and play an important role in the pathogenesis of cerebrovascular diseases. AIMS AND METHODS: In this study the changes of rheological factors--hematocrit (Hct), plasma fibrinogen concentration (PFC), whole blood (WBV) and plasma viscosity (PV), red blood cell aggregation (AI) and deformability and the association between these parameters and cardiovascular risk factors were investigated in 297 patients (173 males, 124 females, mean age: 60 11 years) with chronic phase (3 months after onset) ischemic cerebrovascular diseases, and in 68 healthy volunteers (30 males, 38 females, mean age: 36 6 years). RESULTS: All investigated hemorheological factors were significantly (p < 0.05-0.0001) elevated in cerebrovascular patients compared to normal controls, the rise in Hct, WBV and PV are some of the most prominent findings. In the group of hypertensive, hyperlipidemic patients, smokers and alcoholics Hct, PFC, WBV, PV and AI were significantly (p < 0.05-0.0001) higher compared to healthy controls, the same factors except plasma fibrinogen concentration showed association with diabetic history. Comparing cerebrovascular patients with or without risk factors, the most severe hemorheological deficit was observed in patients with hyperlipidemia and smoking habits. CONCLUSIONS: In this study the authors proved in chronic ischemic cerebrovascular patients that hemorheological abnormalities persist in most cases for a long time after an acute stroke, significant correlation could be seen between blood rheology and cardiovascular risk factors. Examination of rheological parameters can support to choose the optimal medical treatment in the secondary prevention of stroke, correction of hemorheological disturbances can reduce the risk of recurrent stroke.


Assuntos
Doenças Cardiovasculares/fisiopatologia , Hemorreologia , Acidente Vascular Cerebral/prevenção & controle , Acidente Vascular Cerebral/fisiopatologia , Adulto , Idoso , Alcoolismo/complicações , Viscosidade Sanguínea , Doenças Cardiovasculares/sangue , Estudos de Casos e Controles , Transtornos Cerebrovasculares/fisiopatologia , Complicações do Diabetes , Agregação Eritrocítica , Deformação Eritrocítica , Feminino , Fibrinogênio/metabolismo , Hematócrito , Humanos , Hiperlipidemias/complicações , Masculino , Pessoa de Meia-Idade , Plasma , Fatores de Risco , Fumar/efeitos adversos , Acidente Vascular Cerebral/sangue , Acidente Vascular Cerebral/etiologia
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