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1.
Minim Invasive Neurosurg ; 53(5-6): 273-4, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21302197

RESUMO

BACKGROUND: Third ventricle colloid cysts are regarded as benign lesions. They may, however, present with dramatic and rapidly deteriorating neurological signs, leading to sudden death. Although the exact cause of this clinical course is unknown, acute hydrocephalus caused by occlusion of Monro's foramina has been suggested. This, in turn, may be the result of acute cyst swelling, which can exceptionally be due to an intralesional hemorrhage. CASE REPORT: This report illustrates the case of a young patient who deteriorated to sudden coma and was found to have a hemorrhagic colloid cyst of the third ventricle. This was removed via a purely endoscopic technique. Although the radiological results were excellent, the clinical outcome was poor. CONCLUSIONS: This case suggests once again the importance of the early recognition of colloid cysts of the third ventricle for appropriate treatment before potentially irreversible neurological deterioration sets in.


Assuntos
Neoplasias do Ventrículo Cerebral/complicações , Cistos Coloides/complicações , Coma/etiologia , Hidrocefalia/etiologia , Terceiro Ventrículo/patologia , Adulto , Neoplasias do Ventrículo Cerebral/patologia , Cistos Coloides/patologia , Coma/patologia , Feminino , Humanos , Hidrocefalia/complicações , Hidrocefalia/patologia , Neoplasias Neuroepiteliomatosas/complicações , Neoplasias Neuroepiteliomatosas/patologia
2.
Neuroepidemiology ; 21(4): 187-93, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12065881

RESUMO

We carried out an ecological study in the most archaic area of Sardinia to obtain a reliable estimate of the prevalence of multiple sclerosis (MS) and to investigate the geographical variation in the prevalence across the 100 administrative communes. To estimate the area-specific prevalence rate, we adopted a Bayesian approach that makes it possible to filter out the random variation from the estimates and to obtain a map that reflects the true geographical variation in MS prevalence. 428 resident cases were identified by the case register, including 69 multiplex families. The overall prevalence was 157 per 100,000 inhabitants. The Bayesian area-specific prevalence ranged from 143 to 262/100,000. The high prevalence and its moderate geographical variation in a genetically homogeneous population, as well as the high number of multiplex families observed in the communes with the highest prevalence, could be interpreted as representing a high susceptibility of the population to MS.


Assuntos
Esclerose Múltipla/epidemiologia , Adolescente , Adulto , Distribuição por Idade , Idoso , Teorema de Bayes , Suscetibilidade a Doenças , Feminino , Humanos , Itália/epidemiologia , Masculino , Pessoa de Meia-Idade , Prevalência , Medição de Risco , Distribuição por Sexo
3.
Genet Epidemiol ; 20(2): 271-83, 2001 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11180452

RESUMO

Association and linkage studies have established the importance of the major histocompatibility complex (MHC) in the susceptibility for multiple sclerosis (MS). We carried out a case-control study to investigate the ancestral haplotype A30B18DR3 and MS in the Nuoro population of Sardinia, which is isolated and genetically distinct from other populations in the Mediterranean basin and characterized by genetic homogeneity, high level of inbreeding, low migration, high prevalence of MS, high frequency of the relevant haplotype, and high past malaria prevalence. Cases and controls were serologically typed for the currently recognized HLA-A, B, and DR antigens. We used a log-linear approach to fit a wide class of models. We tested our hypothesis comparing different models via a likelihood ratio test. We overcame the complication due to unknown gametic phase using expectation-maximization (EM) algorithm as the estimation method. We estimated confidence intervals for odds ratio by using a profile likelihood approach. We found that: (1) the ancestral haplotype A30B18DR3 was associated to MS after allowing for a possible stratification in cases and controls; (2) DR3 allele was conditional independent on disease status, given A30B18 haplotype; (3) there was a tendency for ORs for the high-risk haplotypes to be higher in the high malaria strata; however, this indication did not achieve statistical significance (P = 0.11).


Assuntos
Antígenos HLA-A , Antígenos HLA-B , Antígeno HLA-DR3 , Haplótipos , Esclerose Múltipla/genética , Alelos , Estudos de Casos e Controles , Etnicidade/genética , Frequência do Gene , Antígenos HLA-A/genética , Antígenos HLA-B/genética , Antígeno HLA-B18 , Antígeno HLA-DR3/genética , Humanos , Itália/epidemiologia , Malária/epidemiologia , Esclerose Múltipla/etnologia , Esclerose Múltipla/imunologia , Prevalência , Projetos de Pesquisa , Estatística como Assunto
4.
Funct Neurol ; 9(6): 297-301, 1994.
Artigo em Inglês | MEDLINE | ID: mdl-7789869

RESUMO

122 patients with acute stroke were examined in order to demonstrate the sensitivity and the specificity of EEG versus CT findings, in distinguishing cortical from subcortical lesions. To do this the electroencephalographic diagnosis performed by two different electroencephalographers was compared with the neuroimaging diagnosis. The results showed a sensitivity of 77% and a specificity of 75%. Furthermore, the EEG findings can also provide physiopathological data, in that the cortical lesions are likely to be due to embolism, while the subcortical lesions are more likely to be due to the pathological process of the intracerebral blood-vessels and the lesions of the watershed territories to hemodynamic phenomena.


Assuntos
Encéfalo/fisiopatologia , Transtornos Cerebrovasculares/fisiopatologia , Eletroencefalografia/métodos , Tomografia Computadorizada por Raios X/métodos , Adulto , Idoso , Artérias Cerebrais/fisiopatologia , Diagnóstico Diferencial , Feminino , Lateralidade Funcional , Humanos , Masculino , Pessoa de Meia-Idade
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