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1.
Folia Neuropathol ; 37(1): 34-42, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-10337062

RESUMEN

Post-mortem neuropathological investigations of the cerebellum were carried out in 15 patients deceased due to lymphoblastic lymphoma (LBL). In patients with survival time of LBL longer than 20 months, neuronal structures of the cerebellum appeared to be significantly rarefied. It was especially observed within granular layer, less frequently in Purkinje and dentate nuclei cells. In cases with longer survival time shrinkage and deformation of neurons, especially Purkinje and dentate nuclei cells were observed. The morphometric analysis suggests that the cerebellar neuronal changes might be a consequence of remote effects of LBL on nervous tissue. The longer survival time contribute to the nervous system exposure on remote effects of neoplasm. The dentate nuclei cells are damaged due to remote effect of lymphoma, irrespective of Purkinje cells destruction.


Asunto(s)
Neoplasias Cerebelosas/mortalidad , Neoplasias Cerebelosas/patología , Diagnóstico por Computador/métodos , Leucemia-Linfoma Linfoblástico de Células Precursoras/mortalidad , Leucemia-Linfoma Linfoblástico de Células Precursoras/patología , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Tasa de Supervivencia , Factores de Tiempo
2.
Folia Neuropathol ; 33(1): 59-65, 1995.
Artículo en Inglés | MEDLINE | ID: mdl-8673423

RESUMEN

The clinical and neuropathological investigations have been done on 133 autopsied patients died of leukemia or non-Hodgkin's lymphoma of high malignancy. A study was performed to analyse the role of various factors particularly with respect to adhesion and aggregation in the CNS leukostasis development. The findings were also designated to evaluate the distribution of leukostasis in different CNS regions and to recognize its intensity in various CNS vessels. Basing on the studies the authors conclude that the risk of CNS leukostasis increases evidently when the leukocyte counts are elevated above 50 G/l. The adhesion and aggregation of leukemic and lymphomatous cells as well as local anatomical factors in the CNS vessels play and important role in the CNS leukostasis development, which is more intensive in the white matter and leptomeninges. The medium-sized vessels are much involved, whereas cortical capillaries are relatively less affected by leukostasis. The CNS leukostasis appears to be dynamic and reversible phenomenon, which undergoes fluctuations according to the leukocyte counts increase or decrease.


Asunto(s)
Encefalopatías/patología , Leucemia/complicaciones , Leucostasis/patología , Linfoma no Hodgkin/complicaciones , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Encefalopatías/sangre , Encefalopatías/etiología , Capilares/patología , Humanos , Recuento de Leucocitos , Leucostasis/sangre , Leucostasis/etiología , Persona de Mediana Edad
3.
Folia Neuropathol ; 33(4): 251-4, 1995.
Artículo en Inglés | MEDLINE | ID: mdl-8673435

RESUMEN

A 14-year-old boy was admitted to our Department due to peripheral palsy of right VII and bilateral of the VI cranial nerves, spasticity, cerebellar symptoms as well as to dysphagia and dysarthria. In general, he was hospitalized 13 times because of the disease of a relapsing-remitting and next progressive course. He died 31 years after onset of the disease. Multiple sclerosis was diagnosed. Brain autopsy revealed tumor involving almost all brain stem structures and a part of right cerebellar hemisphere. Histologically, cavernous angioma was diagnosed.


Asunto(s)
Neoplasias Encefálicas/diagnóstico , Hemangioma Cavernoso/diagnóstico , Esclerosis Múltiple/diagnóstico , Adolescente , Encéfalo/patología , Diagnóstico Diferencial , Resultado Fatal , Humanos , Masculino
4.
Neurol Neurochir Pol ; 17(2): 213-9, 1983.
Artículo en Polaco | MEDLINE | ID: mdl-6633800

RESUMEN

All-night EEG records were obtained in 100 patients aged 14-48 years staying at a neurosurgical centre for various forms of focal epilepsy. In 84 cases discharges were observed during the nocturnal investigation. The morphology of the discharges depended on the phase of sleep during which they appeared. Discharges occurring in phases of light sleep had greater activity and more focal character in relation to the remaining NREM phases. On the other hand, discharges in deep sleep phases had a greater tendency for generalization. In half the cases focal discharges disappeared in the REM sleep phase. Intraseizure changes depended on the phase of sleep, focal or generalized character, and localization of pathological focus. Seiture activity during sleep was never observed in the REM phase of sleep.


Asunto(s)
Corteza Cerebral/fisiopatología , Epilepsia/fisiopatología , Fases del Sueño/fisiología , Potenciales de Acción , Adolescente , Adulto , Electroencefalografía , Epilepsia del Lóbulo Temporal/fisiopatología , Femenino , Lateralidad Funcional/fisiología , Humanos , Masculino , Persona de Mediana Edad
5.
Neurol Neurochir Pol ; 11(3): 367-70, 1977.
Artículo en Polaco | MEDLINE | ID: mdl-196230

RESUMEN

The authors report a case of sporadic secondary amyloidosis with polyneuropathy in a patient aged 50 years. The disease developed during chronic pyelonephritis. The case is described in view of its rare occurrence, diagnostic difficulties and interesting histological findings.


Asunto(s)
Amiloidosis/patología , Encefalopatías/patología , Enfermedades del Sistema Nervioso Periférico/patología , Cerebelo/patología , Corteza Cerebral/patología , Enfermedad Crónica , Femenino , Humanos , Persona de Mediana Edad , Pielonefritis/patología , Médula Espinal/patología
6.
Neurol Neurochir Pol ; 20(5): 410-4, 1986.
Artículo en Polaco | MEDLINE | ID: mdl-3587510

RESUMEN

100 all night sleep records in 90 patients with various forms of epilepsy and 10 patients with syncope were analyzed. There were 10 patients with generalized epilepsy, 41-with partial epilepsy with complex symptomatology and temporal foci, 23--with mixed seizures and frontal focal changes and 16 patients with partial epilepsy with simple seizures and various location of EEG foci. Normal sleep pattern was present in 21% of cases. The most frequent changes of sleep pattern were: prolongation of sleep onset and the latency of the first episode of REM, instability of sleep stages and absence of sleep spindles. Interictal discharges appeared mostly in all sleep stages of NREM. 50% of epileptic patients showed focal spikes in REM. Nocturnal seizures occurred in 18 patients, in several of them very frequently.


Asunto(s)
Epilepsia/fisiopatología , Sueño/fisiología , Adolescente , Adulto , Ritmo Circadiano , Electroencefalografía , Femenino , Humanos , Masculino , Persona de Mediana Edad , Fases del Sueño/fisiología
7.
Neurol Neurochir Pol ; 20(6): 517-22, 1986.
Artículo en Polaco | MEDLINE | ID: mdl-3600970

RESUMEN

The authors carried out follow-up examinations of 75 patients with reversible ischaemic strokes suffered by them 6-10 years earlier. The results showed that reversible ischaemic strokes accounted for about 8% of all strokes. The risk of a repeated stroke was about 10.6%. The prognosis in such cases is rather good, but is worsened by coexistence of risk factors, particularly by coincidence of several such factors. In 17.6% of cases death ensued within 6-10 years.


Asunto(s)
Trastornos Cerebrovasculares/etiología , Ataque Isquémico Transitorio/complicaciones , Adulto , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Recurrencia , Riesgo
8.
Neurol Neurochir Pol ; 19(6): 508-11, 1985.
Artículo en Polaco | MEDLINE | ID: mdl-3835491

RESUMEN

The authors report two cases of dyssynergia cerebellaris myoclonica in siblings. Apart from typical clinical manifestations attention is called to the results of computerized tomography of the brain which demonstrated cerebellar atrophy. This helped in verification of the diagnosis. Comparing these cases with other ones described earlier in the literature the authors conclude that dyssynergia cerebellaris myoclonica is not a separate nosological entity but a syndrome associated with myoclonia.


Asunto(s)
Ataxia Cerebelosa/diagnóstico , Disinergia Cerebelosa Mioclónica/diagnóstico , Mioclonía/fisiopatología , Humanos , Masculino , Persona de Mediana Edad , Disinergia Cerebelosa Mioclónica/genética , Mioclonía/genética
9.
Neurol Neurochir Pol ; (5-6): 333-8, 1982.
Artículo en Polaco | MEDLINE | ID: mdl-6961294

RESUMEN

Twenty-one patients with acute leukaemias were studied carrying out cytological investigations of the cerebrospinal fluid and then postmortem neuropathological examinations. The aim of the study was a comparison of these results. No correlation was demonstrated between CSF changes and the extent and location of leukaemic infiltrates in the meninges and the brain. In cases of subarachnoid haemorrhage the intensity of CSF changes was proportional to the extent of subarachnoid haemorrhage but was independent of its location.


Asunto(s)
Neoplasias Cerebelosas/líquido cefalorraquídeo , Líquido Cefalorraquídeo/citología , Leucemia Linfoide/líquido cefalorraquídeo , Neoplasias Meníngeas/líquido cefalorraquídeo , Piamadre/patología , Adolescente , Adulto , Neoplasias Cerebelosas/patología , Cerebelo/patología , Humanos , Leucemia Linfoide/patología , Neoplasias Meníngeas/patología , Persona de Mediana Edad
10.
Neurol Neurochir Pol ; 29(6): 835-44, 1995.
Artículo en Polaco | MEDLINE | ID: mdl-8714722

RESUMEN

The authors review data on sumatriptan obtained in the results of their own studies performed on 78 patients in 10 Polish neurological centres. In all 154 migraine attacks were treated with 6 mg of subcutaneous sumatriptan. Significant decrease of pain intensity was achieved in 30% of cases after 15 min and 60%--after 30 min. According to the patient's own opinion, 62% of them evaluated the drug as very efficient, 23% of patients--as efficient. Adverse effects were reported by 11 patients (15%), but they were mild and transient. Headache recurred in 16% of patients.


Asunto(s)
Trastornos Migrañosos/tratamiento farmacológico , Sumatriptán/uso terapéutico , Vasoconstrictores/uso terapéutico , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad
11.
Neurol Neurochir Pol ; 35(3): 395-404, 2001.
Artículo en Polaco | MEDLINE | ID: mdl-11732263

RESUMEN

27 patients (22 women, 5 men); age 17 to 56 yr. (mean age 37 yr.) were included in this study, 4 had primary antiphospholipid syndrome and 18 secondary antiphospholipid syndrome in the course of systemic connective tissue disease and in 5 cases increased levels of anticardiolipid antibodies were found which did not meet the criteria necessary for diagnosis of secondary antiphospholipid syndrome. The mean duration of the disease was 8 yrs. Among primary antiphospholipid syndrome patients two had ischaemic stroke, one migraine-like headache and seizures. 18 patients had lupus erythematosus, two mixed connective tissue disease, one rheumatoid arthritis, one Sjögren syndrome, one Behçet disease. In 55% of patients migraine-like headache, polyneuropathies, encephalophaties, stroke, seizures and vision disturbances were present. In 18.5% of patients EEG exam revealed focal lesions with tendency for generalisation. On brain stem auditory evoked potentials examination, in 11.1% of patients conductivity lesions in mesencephalon and pons were found, visual evoked potentials, in 11.1% of patients in visual tracts. In 37% of patients, neuropathy was found on EMG exam. Neurological symptoms are one of the most frequent disorders in systemic connective tissue disease associated with the presence of anicardiolipin antibodies.


Asunto(s)
Anticuerpos Anticardiolipina/inmunología , Síndrome Antifosfolípido/complicaciones , Síndrome Antifosfolípido/inmunología , Isquemia Encefálica/complicaciones , Adolescente , Adulto , Encéfalo/irrigación sanguínea , Isquemia Encefálica/diagnóstico , Enfermedades del Tejido Conjuntivo/complicaciones , Enfermedades del Tejido Conjuntivo/inmunología , Electroencefalografía , Electromiografía , Ensayo de Inmunoadsorción Enzimática , Potenciales Evocados Auditivos del Tronco Encefálico/fisiología , Potenciales Evocados Visuales/fisiología , Extremidades/fisiopatología , Femenino , Humanos , Masculino , Mesencéfalo/fisiopatología , Persona de Mediana Edad , Conducción Nerviosa/fisiología , Puente/fisiopatología
12.
Neurol Neurochir Pol ; 23(1): 1-6, 1989 Jan.
Artículo en Polaco | MEDLINE | ID: mdl-2685628

RESUMEN

The authors present an analysis of the clinical course of 6 cases of Creutzfeldt-Jakob disease (patients were aged from 27 to 59 years). The diagnosis was established during the life of the patients. In the neurological status dementia and syndromes of pyramidal and extrapyramidal lesions predominated. Neuropathological examinations in 5 cases demonstrated also considerable cerebellar damage, however, clinical signs of this damage were noted in two patients only. EEG findings were of greatest importance among the laboratory investigations.


Asunto(s)
Síndrome de Creutzfeldt-Jakob/diagnóstico , Adulto , Enfermedades de los Ganglios Basales/clasificación , Enfermedades de los Ganglios Basales/diagnóstico , Enfermedades Cerebelosas/diagnóstico , Síndrome de Creutzfeldt-Jakob/clasificación , Demencia/clasificación , Demencia/diagnóstico , Diagnóstico Diferencial , Electroencefalografía , Femenino , Humanos , Masculino , Persona de Mediana Edad
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