ABSTRACT
ABSTRACT Objective To analyze cases of recurrent glioblastoma subjected to reoperation at a Brazilian public healthcare service. Methods A total of 39 patients subjected to reoperation for recurrent glioblastoma at the Department of Neurosurgery, São Paulo Hospital, Federal University of São Paulo, from January 2000 to December 2013 were retrospectively analyzed. Results The median overall survival was 20 months (95% confidence interval – CI = 14.9–25.2), and the median survival after reoperation was 9.1 months (95%CI: 2.8–15.4). The performance of adjuvant treatment after the first operation was the single factor associated with overall survival on multivariate analysis (relative risk – RR = 0.3; 95%CI = 0.2–0.7); p = 0.005). Conclusion The length of survival of patients subjected to reoperation for glioblastoma at a Brazilian public healthcare service was similar to the length reported in the literature. Reoperation should be considered as a therapeutic option for selected patients.
RESUMO Objetivo Analisar o papel da reoperação em pacientes com glioblastoma recidivado em um serviço público no Brasil. Métodos Foram analisados retrospectivamente 39 pacientes submetidos à reoperação por recorrência de glioblastoma no Departamento de Neurocirurgia da Universidade Federal de São Paulo, no período de janeiro de 2000 até dezembro de 2013. Resultados A sobrevida global mediana foi de 20 meses (IC 95% = 14.9–25.2), e a sobrevida mediana após a reoperação foi de 9.1 meses (IC 95% = 2.8–15.4). A realização de tratamento adjuvante após a primeira cirurgia foi o único fator associado com a sobrevida global numa análise multivariada (RR = 0.3; IC 95% = 0.2–0.7; p = 0.005). Conclusão A sobrevida dos pacientes submetidos à reoperação em um serviço público no Brasil é semelhante à reportada pela literatura. A reoperação deve ser considerada como uma opção terapêutica em pacientes selecionados.
Subject(s)
Humans , Male , Female , Adult , Middle Aged , Aged , Young Adult , Reoperation/mortality , Brain Neoplasms/mortality , Glioblastoma/mortality , Neoplasm Recurrence, Local/mortality , Reoperation/standards , Time Factors , Brain Neoplasms/surgery , Brain Neoplasms/therapy , Survival Analysis , Retrospective Studies , Glioblastoma/surgery , Glioblastoma/therapy , Neoplasm, Residual , Chemoradiotherapy, Adjuvant/methods , Neoplasm Recurrence, Local/surgeryABSTRACT
INTRODUCTION: In this study the authors review the outcomes of 22 patients with medically refractory epilepsy and slow growth brain tumors. OBJECTIVES: Evaluate the clinical, electrophysiological, operative, and histopathological features. PATIENTS AND RESULTS: The majority of the tumors were located in the temporal lobe (n = 20) and involved the cortical gray matter. The most frequent tumors were gangliogliomas (n = 9), astrocytomas grade I and II (n = 6), dysembryoplastic neuroepithelial tumors (n = 5) and ganglioneuroma (n = 2). The biological behavior of the tumors was strikingly indolent, as indicated by a long preoperative history of chronic seizures (mean, 14 years). Mean follow-up time after resection was 27 months, and according to EngelÆs classification, 85 percent were seizure-free, 10 percent showed a reduction of seizure frequency of at least 90 percent, and 5 percent had reduction in seizure frequency at least 75 percent. CONCLUSION: The data indicate that neoplasms associated with pharmacoresistent epilepsy constitute a distinct clinicopathological group of tumors that arise in young patients, involve the cortex, and exhibit indolent biological behavior for many years. Complete surgical removal of these tumors, including the epileptogenic area, can achieve excellent seizure control.
INTRODUÇÃO: Neste estudo os autores avaliaram retrospectivamente 22 pacientes tratados cirurgicamente com diagnóstico de epilepsia refratária e tumor cerebral de crescimento lento. OBJETIVOS: Avaliar os aspectos clínicos, eletrofisiológicos, cirúrgicos e histopatológicos. PACIENTES E RESULTADOS: A maioria dos tumores estava localizada no lobo temporal (n = 20) com envolvimento da substância cinzenta. Ganglioglioma foi o tumor mais frequente (n = 9), seguido do astrocitoma grau I e II OMS (n = 6), tumor neuroepitelial disembrioplástico (DNET) (n = 5) e ganglioneuroma (n = 2). O comportamento biológico dos tumores foi estritamente indolente como indicado pela longa história pré-operatória de (média, 14 anos). O tempo de acompanhamento pós-operatório médio foi de 27 meses e de acordo com a Classificacão de Engel, 85 por cento ficaram sem crises (Classe I), 10 por cento obtiveram redução maior de 90 por cento das crises (Classe II), e 5 por cento tiveram redução menor que 75 por cento (Classe III). CONCLUSÃO: Os dados indicam que neoplasias associadas à epilepsia crônica refratária constituem um grupo de tumores com características clinico-patológicas distintas que se iniciam em pacientes jovens, envolvem o córtex e apresentam comportamento biológico indolente. A ressecção cirúrgica completa destes tumores, incluindo a zona epileptogênica, levou ao controle total das crises na maior parte dos casos estudados.
Subject(s)
Brain Neoplasms/surgery , Epilepsy/surgery , Phenobarbital/adverse effects , Phenytoin/adverse effects , Carbamazepine/adverse effects , Retrospective StudiesABSTRACT
Entre os pacientes operados no Hospital São Paulo e acompanhados pelo setor de neuro-oncologia no período de 1991 a 2000, avaliamos a apresentaçäo clínica, aspectos de imagem e características histopatológicas de 4 pacientes (2 homens; idade entre 15 e 52 anos) cujo diagnóstico histológico foi malformaçäo vascular associada a glioma. O quadro inicial foi cefaléia progressiva com características de hipertensäo intracraniana (em 3) e crises parciais motoras (em 1). O diagnóstico tomográfico inicial foi processo expansivo, sem que houvesse suspeita de malformaçäo vascular pelo aspecto da imagem em nenhum caso. O exame histológico mostrou neoplasias de linhagem astrocítica associadas a malformações vasculares. Em nenhum paciente o componente vascular esteve localizado na intimidade da neoplasia. A associaçäo de malformaçäo vascular e gliomas é rara e deve ser caracterizada por nítida separaçäo entre a malformaçäo e a neoplasia, independente da vascularizaçäo própria do tumor
Subject(s)
Humans , Adolescent , Adult , Female , Middle Aged , Brain Neoplasms , Glioma , Intracranial Arteriovenous Malformations , Brain Neoplasms , Glioma , Intracranial Arteriovenous Malformations , Magnetic Resonance Imaging , Tomography, X-Ray ComputedABSTRACT
OBJECTIVE: Neurologic complications are known as important cause of morbidity and mortality in orthotopic heart transplantation. Our aim was to identify the frequency and outcome of neurologic complications after heart transplantation in a prospective observational study. METHOD: From September 93 to September 99, as part of our routine heart transplantation protocol all patients with end-stage cardiac failure were evaluated by the same neurologist before and at the time of any neurologic event (symptom or complaint) after transplantation. RESULTS: Out of 120 candidates evaluated, 62 were successfully transplanted (53 male; median age 45.5 years, median follow-up 26.8 months). Fifteen patients (24 percent) had ischemic, 22 (35 percent) idiopathic, 24 (39 percent) Chagas' disease and 1 (2 percent) had congenital cardiomyopathy. Neurologic complications occurred in 19 patients (31 percent): tremor, severe headache, transient encephalopathy and seizures related to drug toxicity or metabolic changes in 13; peripheral neuropathy in 4; and spinal cord compression in two (metastatic prostate cancer and epidural abscess). No symptomatic postoperative stroke was observed. CONCLUSIONS: Although frequent, neurologic complications were seldom related to persistent neurologic disability or death. Most of the complications resulted from immunosuppression, however, CNS infection was rare. The absence of symptomatic stroke in our series may be related to the lower frequency of ischemic cardiomyopathy
Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Heart Transplantation , Nervous System Diseases , Cardiomyopathies , Cerebrovascular Disorders , Follow-Up Studies , Prospective Studies , Risk FactorsABSTRACT
Coronary artery bypass surgery (CABG) without cardiopulmonary bypass (CPB) may potentially reduce the number of microembolic signals (MES) associated with aortic manipulation or generated by the pump circuit, resulting in a better neurologic outcome after surgery. Our aim was to compare the frequency of MES and neurologic complications in CABG with and without CPB. Twenty patients eligible to routine CABG without CPB were randomized to surgery with CPB and without CPB and continuously monitored by transcranial Doppler. Neurologic examination was performed in all patients before and after surgery. The two groups were similar with respect to demographics, risk factors, grade of aortic atheromatous disease and number of grafts. The frequency of MES in the nonCPB group was considerably lower than in CPB patients, however, we did not observe any change in the neurologic examination during the early postoperative period. Neurologic complications after CABG may be related to the size and composition of MES rather than to their absolute numbers. A large prospective multicentric randomized trial may help to elucidate this complex issue
Subject(s)
Humans , Male , Female , Middle Aged , Cardiopulmonary Bypass , Coronary Artery Bypass , Intracranial Embolism , Intraoperative Complications , Aortic Diseases , Aortic Diseases/etiology , Intracranial Embolism/etiology , Intraoperative Complications/etiology , Postoperative Period , Risk Factors , Ultrasonography, Doppler, TranscranialABSTRACT
Uma mulher de 45 anos apresentou quadro de perda da iniciativa, dificuldade de memória, choro imotivado e distúrbio de comportamento, rapidamente progressivos ao longo de 6 meses, quando tornou-se näo responsiva a estímulos verbais e totalmente apática. Um EEG mostrou atividade periódica bilateral, sugerindo doença de Creutzfeldt-Jacob (DCJ), mas a investigaçäo para outras causas de demência mostrou hipercalcemia e hipofosfatemia que, exames posteriores, indicaram dever-se adenoma de células oxífilas de paratireóide. Com a correçäo do distúrbio eletrolítico e posterior cirurgia houve normalizaçäo tanto do EEG como do exame neurológico. Näo temos conhecimento de outros relatos de hiperparatirecidismo associado a síndrome demencial e atividade periódica no EEG. Este deveria ser um diagnóstico diferencial em todos os casos de DCJ recente
Subject(s)
Middle Aged , Humans , Female , Creutzfeldt-Jakob Syndrome/diagnosis , Hyperparathyroidism/diagnosis , Creutzfeldt-Jakob Syndrome/etiology , Diagnosis, Differential , Electroencephalography , Hyperparathyroidism/complications , Tomography, X-Ray ComputedABSTRACT
Os autores apresentaram um caso de doença de Behçet com comprometimento auditivo e vestibular, com a presença de sinais sugestivos de localizaçäo central a pesquisa otoneurológica. Devido a ocorrência de manifestaçöes cócleo-vestibulares ser rara, procurou-se enfatizar a necessidade de uma pesquisa otoneurológica acurada