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Objective To describe our surgical techniques, analyze their safety and their postoperative outcomes for foramen magnum tumors (FMTs). Methods From 1986 to 2014, 34 patients with FMTs underwent surgeries using either the lateral suboccipital approach, standard midline suboccipital craniotomy, or the far lateral approach, depending on the anatomic location of the lesions. Results In the present series, there were 22 (64.7%) female and 12 (35.2%)male patients. The age of the patients ranged from12 to 63 years old.We observed 1 operativemortality (2.9%). A total of 28 patients (82.3%) achieved a score of 4 or 5 in the Glasgow Outcome Scale (GOS). Gross total resection (GTR) was obtained in 22 (64.7%) patients. After the surgery, 9 (26%) patients developed lower cranial nerve dysfunction (LCNd) weakness. The follow-up varied from 1 to 24 years (mean: 13.2 years). Conclusion Themajority of tumors located in the FMcan be safely and efficiently removed usingeither thelateral suboccipital approach, standardmiddlelinesuboccipital craniotomy, or the far lateral approach, depending on the anatomic location of the lesions.
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Procedimientos Neuroquirúrgicos/métodos , Foramen Magno/cirugía , Neoplasias Meníngeas/cirugía , Meningioma/cirugía , Registros Médicos , Estudios Retrospectivos , Resultado del Tratamiento , Craneotomía/métodos , Foramen Magno/anomalías , Foramen Magno/fisiopatología , Meningioma/patologíaRESUMEN
Background To describe our operative strategy and analyze its safety and effectiveness for the removal of medial sphenoid wing meningiomas (MSWMs) through the extended pterional approach. Method We identified 47 patients with MSWMs who were operated using this approach between 1986 and 2016. Medical charts, operative reports, imaging results, and clinical follow-up evaluations were reviewed and retrospectively analyzed. Results No surgical mortality was observed in this sample. Gross total resection was achieved in 30 (63.8%) patients. Intradural clinoidectomy was performed in 16 (34%) patients. The median length of follow-up was 8.5 years (range, 1-30 years). Conclusion The extended pterional approach associated with microsurgery techniques provided excellent results for the removal of MSWMs.
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OBJECTIVE: The objective of the study was to describe our approach and the surgical technique and analyze its safety and the outcome for foramen magnum meningiomas (FMMs). METHODS: From 1986 to 2016, 15 FMM patients were operated on using the lateral suboccipital retrocondylar approach. RESULTS: In this series, there were 12 (80%) female and 3 (20%) male patients. The patients ranged in age from 33 to 63 years. There was no operative dead, but two patients died during the follow-up period, which varied from 1 to 24 years (mean, 10.2 years). Twelve patients (80%) achieved Glasgow Outcome Scale 4 or 5. Gross total resection was achieved in 13 (86.6.7%) patients. CONCLUSIONS: The majority of FMM can be safely removed using the lateral suboccipital retrocondylar approach without condylar resection, associated to meticulous microsurgical technique.
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Background The purpose of this article is to describe our approach, surgical strategies, and results for resection of meningiomas located at cerebellopontine angle (CPA). Methods We retrospectively identified 28 patients with CPA meningiomas operated by the extended retrosigmoid approach. This approach incorporates a generous mastoidectomy and the sigmoid sinus exposure. Results The mean age was 33.8 years, with a follow-up of 12.5 years. Gross total removal (GTR) was achieved in 22 (78.5%) patients with low surgical mortality, acceptable morbidity, and recurrence rate of 7.1% (2 patients). Conclusion The extended retrosigmoid approach enhances the exposure of the CPA and posterior fossa cisterns and increases the surgical angle of maneuverability. This approach provides adequate access even to extensive CPA meningiomas, enabling, in most of cases, GTR to be safe and effective. The extended retrosigmoid approach used in this group of patients is an alternative to more extensive cranial base approaches.
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Objective The aim of this paper is to describe our surgical strategy and technique and to identify the best management for posterior fossa dermoid and epidermoid tumors (PFDETs). Methods We retrospectively identified 21 consecutive patients (11 males and 10 females), with a mean age of 33.2 years, a mean follow-up of 6.1 years, and pathologically confirmed PFDETs. Total 17 patients were submitted to the extended retrosigmoid approach. This approach incorporates transverse sigmoid sinus exposure and a generous mastoidectomy. Results Gross total tumor removal was achieved in 16 (76.1%) cases, with no surgical mortality and a recurrence rate of 9.5%. Conclusions The surgical strategies used in this group of patients enabled the total removal of most tumors without surgical mortality and with minimal morbidity and recurrence rates. The extended retrosigmoid approach used is an alternative path regarding cranial base approaches. This approach is quick, simple and safe, and decreases the retraction of the cerebellum.
Objetivos O objetivo deste estudo é descrever a técnica operatória para a melhor abordagem dos tumores dermoides e epidermoides da fossa posterior. Métodos Foram analisados retrospectivamente 21 pacientes (11 masculinos e 10 femininos), com idade média de 33,2 anos e acompanhamento de 6,1 anos, com diagnóstico histopatológico de tumor dermoide ou epidermoide de fossa posterior. Nesse grupo, 17 pacientes foram submetidos a abordagem retrossigmoide estendida. Esta abordagem inclui exposição do seio transverso e sigmoide, além de ampla mastoidectomia. Resultados Remoção cirúrgica total foi alcançada em 16 (76,1%) casos sem mortalidade e com recidiva em 9,5% dos casos. Conclusões As abordagens cirúrgicas utilizadas nesta série permitiram a ressecção total na maioria dos pacientes, sem mortalidade cirúrgica e com morbidade e recorrência mínima. A craniotomia retrossigmoide estendida utilizada é uma boa alternativa para abordagens da base do crânio. É uma abordagem simples, rápida, segura, e que minimiza a retração do cerebelo.
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Humanos , Masculino , Femenino , Neoplasias Encefálicas , Carcinoma de Células Escamosas , Fosa Craneal Posterior , Quiste Dermoide , Procedimientos Quirúrgicos Operativos/métodosRESUMEN
BACKGROUND: The occurrence of a brain tumor or intracranial vascular lesion during pregnancy is a rare event, but when it happens, it jeopardizes the lives of both the mother and infant. It also creates challenges of a neurosurgical, obstetric, and ethical nature. A multidisciplinary approach should be used for their care. METHODS: Between 1986 and 2015, 12 pregnant women diagnosed with brain tumors and 17 women with intracranial vascular lesion underwent treatment at the Neurosurgery Department of the Servidores do Estado Hospital and Rede D'Or/São Luis. The Neurosurgery Department teamed up with Obstetrics Anesthesiology Departments in establishing the procedures. The patients' records, surgical descriptions, imaging studies, and histopathological material were reviewed. RESULTS: Among 12 patients presenting with brain tumors, there were neither operative mortality nor fetal deaths. Among the vascular lesions, aneurysm rupture was responsible for bleeding in 6 instances. Arteriovenous malformation was diagnosed in 7 patients. In this subgroup, the maternal and fetal mortality rates were 11.7% and 23.7%, respectively. CONCLUSIONS: We can assert that the association between a brain tumor and vascular lesions with pregnancy is a very unusual event, which jeopardizes both the lives of the mother and infant. It remains incompletely characterized due to the rare nature of these potentially devastating events. Knowing the exact mechanism responsible for the interaction of pregnancy and with these lesions will improve the treatment of these patients.
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Objective The aim of this paper is to observe if the extended pterional approach for the removal of craniopharyngiomas is safe and effective. The mortality, morbidity, and recurrence rates are presented and discussed. Method This is a retrospective analysis of 29 craniopharyngioma patients who underwent surgery between January 1988 and December 2014 at the Department of Neurosurgery of the Hospital Federal dos Servidores do Estado, Rio de Janeiro, Brazil. The charts, operative reports and imaging studies were reviewed. Results We identified 17 males (58.6%) and 12 females (41.3%) ranging in age from 0.6 to 84 years (mean 57.4 years). Thirteen (44.8%) patients were infants or adolescents. Surgical mortality occurred in one patient (3.4%). Gross total tumor removal was achieved in 15 (51.7%) patients. The median follow-up time was 7.1 years. Conclusion The extended pterional approach provides adequate access to craniopharyngiomas, and the majority of lesions could be totally removed, with a low mortality rate, but the best treatment for craniopharyngiomas remains controversial.
Objetivo Observar se a craniotomia pterional estendida é uma técnica segura e efetiva. Método É um estudo retrospectivo de 29 pacientes com craniofaringiomas que foram submetidos a craniotomia pterional estendida entre 1988 e 2014. As imagens e os prontuários foram analisados. Resultados Esse grupo é composto por 17 homens (58,6%) e 12 mulheres (41,3%), e a idade variou de 0,6 a 84 anos (media 57,4 anos). Treze (44,8%) pacientes eram crianças ou adolescentes. A remoção total da lesão ocorreu em 15 (51,7%) indivíduos. A mortalidade cirúrgica: um paciente (3,4%). O follow-up médio é de 7,1 anos. Conclusão A craniotomia pterional estendida permitiu a remoção total da lesão na maioria dos pacientes, com baixa mortalidade, porém o melhor tratamento para o craniofaringioma ainda gera muita controvérsia.
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Craneofaringioma/cirugía , Craneotomía , Microcirugia/métodos , Craneofaringioma/patologíaRESUMEN
Objective To describe a unique operative strategy, instead the classical pterional approach, and to analyses it safety and effectiveness for removal of anterior cranial fossa meningiomas. Method We identify 38 patients with tuberculum sellae and olphactory groove meningiomas operated between 1986 and 2013. Medical charts, operative reports, imaging studies and clinical follow-up evaluations were reviewed and analyzed retrospectively. The pterional craniotomy is extended toward the frontal bone providing access through the subfrontal route, besides the usual anterolateral view provided by the classical pterional approach. Results Surgical mortality occurred in one patient (2.6%). Gross total resection was achieved in 27 patients (86.8%). Median time of follow-up was 69.4 months. Conclusion The extended pterional approach allows excellent results. Total removal of meningiomas of the anterior cranial fossa was obtained in 86.8 % of patients, with low morbidity and mortality.
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Fosa Craneal Anterior/cirugía , Neoplasias Meníngeas/cirugía , Meningioma/cirugía , Microcirugia/métodos , Procedimientos Neuroquirúrgicos/métodos , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Niño , Craneotomía/métodos , Craneotomía/mortalidad , Femenino , Estudios de Seguimiento , Humanos , Masculino , Neoplasias Meníngeas/mortalidad , Meningioma/mortalidad , Microcirugia/mortalidad , Persona de Mediana Edad , Procedimientos Neuroquirúrgicos/mortalidad , Estudios Retrospectivos , Silla Turca/cirugía , Resultado del Tratamiento , Adulto JovenRESUMEN
ABSTRACT Objective To describe a unique operative strategy, instead the classical pterional approach, and to analyses it safety and effectiveness for removal of anterior cranial fossa meningiomas. Method We identify 38 patients with tuberculum sellae and olphactory groove meningiomas operated between 1986 and 2013. Medical charts, operative reports, imaging studies and clinical follow-up evaluations were reviewed and analyzed retrospectively. The pterional craniotomy is extended toward the frontal bone providing access through the subfrontal route, besides the usual anterolateral view provided by the classical pterional approach. Results Surgical mortality occurred in one patient (2.6%). Gross total resection was achieved in 27 patients (86.8%). Median time of follow-up was 69.4 months. Conclusion The extended pterional approach allows excellent results. Total removal of meningiomas of the anterior cranial fossa was obtained in 86.8 % of patients, with low morbidity and mortality.
RESUMO Objetivo Descrever a craniotomia pterional estendida, ao invés da abordagem pterional clássica, e analisar sua segurança e eficácia para a remoção dos meningiomas da fossa anterior. Método Identificamos 38 pacientes com meningiomas do tubérculo da sela e da goteira olfatória operados entre 1986 e 2013. Os prontuários, relatórios cirúrgicos, exames de imagem e acompanhamento pós-operatório foram analisados retrospectivamente. A craniotomia pterional com extensão para o osso frontal permite acesso pela via subfrontal além da via anterolateral do acesso pterional clássico. Resultados A mortalidade cirúrgica foi de 2,6% (um paciente). A remoção total foi alcançada em 86,8% (27 pacientes) com um tempo médio de seguimento de 69,4 meses. Conclusão A abordagem pterional estendida permite excelentes resultados. A remoção total dos meningiomas da fossa craniana anterior foi obtida em 86,8% dos pacientes, com baixa morbi-mortalidade.
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Humanos , Masculino , Femenino , Niño , Adolescente , Adulto , Persona de Mediana Edad , Anciano , Anciano de 80 o más Años , Adulto Joven , Procedimientos Neuroquirúrgicos/métodos , Fosa Craneal Anterior/cirugía , Neoplasias Meníngeas/cirugía , Meningioma/cirugía , Microcirugia/métodos , Silla Turca/cirugía , Estudios Retrospectivos , Estudios de Seguimiento , Resultado del Tratamiento , Procedimientos Neuroquirúrgicos/mortalidad , Craneotomía/métodos , Craneotomía/mortalidad , Neoplasias Meníngeas/mortalidad , Meningioma/mortalidad , Microcirugia/mortalidadRESUMEN
OBJECTIVE: Observe whether a microsurgical gross total removal (GTR) of a spinal nerve sheath tumors (SNSTs) is safe and decreases the tumor recurrence. METHOD: We identify 30 patients with 44 SNSTs. RESULTS: We operated upon 15 males and 15 females patients; mean age 40 years. GTR was achieved in 29 (96.6%) instances. Surgical mortality was 3.3% and the recurrence rate was 3.3%. The median follow-up time was 6.2 years. CONCLUSION: The surgical approach used in this group of patients afford that the great majority of tumors could be totally removed with low mortality and low recurrence rates, proving to be safe and effective.
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Microcirugia/métodos , Neoplasias de la Vaina del Nervio/cirugía , Neurilemoma/cirugía , Neurofibroma/cirugía , Neoplasias de la Columna Vertebral/cirugía , Adolescente , Adulto , Anciano , Niño , Femenino , Humanos , Imagen por Resonancia Magnética , Masculino , Microdisección/métodos , Persona de Mediana Edad , Recurrencia Local de Neoplasia , Neoplasias de la Vaina del Nervio/diagnóstico por imagen , Neurilemoma/diagnóstico por imagen , Neurofibroma/diagnóstico por imagen , Radiografía , Reproducibilidad de los Resultados , Neoplasias de la Columna Vertebral/diagnóstico por imagen , Raíces Nerviosas Espinales/cirugía , Resultado del Tratamiento , Adulto JovenRESUMEN
Objective: Observe whether a microsurgical gross total removal (GTR) of a spinal nerve sheath tumors (SNSTs) is safe and decreases the tumor recurrence. Method: We identify 30 patients with 44 SNSTs. Results: We operated upon 15 males and 15 females patients; mean age 40 years. GTR was achieved in 29 (96.6%) instances. Surgical mortality was 3.3% and the recurrence rate was 3.3%. The median follow-up time was 6.2 years. Conclusion: The surgical approach used in this group of patients afford that the great majority of tumors could be totally removed with low mortality and low recurrence rates, proving to be safe and effective. .
Objetivo: Observar se a ressecção microcirúrgica completa dos shwannomas ou neurofibromas raquianos é uma técnica segura e efetiva. Método: Foram operados 30 pacientes com 44 schwannomas ou neurofibromas intrarraquiano. Resultados: A remoção total da lesão ocorreu em 27 casos (96.6%). A taxa de mortalidade cirúrgica observada nesta série foi de 3.3%. O tempo médio de seguimento foi de 6.2 anos. Conclusão: A estratégia microcirúrgica empregada com esses pacientes propiciou a remoção total dos tumores na maioria dos pacientes, com baixa mortalidade e recidiva tumoral, mostrando ser segura e efetiva. .
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Adolescente , Adulto , Anciano , Niño , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Microcirugia/métodos , Neoplasias de la Vaina del Nervio/cirugía , Neurilemoma/cirugía , Neurofibroma/cirugía , Neoplasias de la Columna Vertebral/cirugía , Imagen por Resonancia Magnética , Microdisección/métodos , Recurrencia Local de Neoplasia , Neoplasias de la Vaina del Nervio , Neurilemoma , Neurofibroma , Reproducibilidad de los Resultados , Neoplasias de la Columna Vertebral , Raíces Nerviosas Espinales/cirugía , Resultado del TratamientoRESUMEN
BACKGROUND: The aim of this paper is to report on our surgical strategy and technique and to identify the best management for intracranial dermoids and epidermoids tumors (IDETs). METHODS: We retrospectively reviewed 33 consecutive patients (14 males and 19 females; mean age at surgery, 37.9 years) with pathologically confirmed IDETs who underwent surgical resection, with mean follow-up of 7.2 years. RESULTS: Gross total tumor removal was achieved in 24 cases (72.7%) with zero surgical mortality and a recurrence rate of 9%. CONCLUSIONS: The surgical strategies used in this group of patients enabled total removal of most tumors without surgical mortality and with low morbidity and recurrence rates, proving to be safe and effective.
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BACKGROUND: Despite the development of microsurgery and cranial base techniques, the surgical management of Foramen Magnum Meningiomas (FMM) continues to be a technical challenge to neurosurgeons. Controversy concerning the utility of systematic condyle drilling for approaching FMM has been raised. Our aim was to describe the surgical technique, analyze its safety, and the postoperative outcome in 12 consecutive FMM patients. METHODS: From 1986 to 2011, 12 patients with FMM underwent operations in the Department of Neurosurgery at Servidores do Estado Hospital and in a private clinic. All patients were operated using a standard suboccipital craniectomy, preserving the occipital condyle, opening of the Foramen Magnum, and ipsilateral removal of the posterior arch of C1. RESULTS: There was no operative mortality, nine patients achieved Glasgow Outcome Scale 4 or 5. Condylar resection was not deemed necessary in any case. Gross total resection was achieved in nine patients. After surgery, four patients developed lower cranial nerve weakness. There was no significant postoperative complication in the remaining patients. The average follow-up is 8.2 years. CONCLUSION: The vast majority of FMM can be safely removed with a retrocondylar lateral suboccipital approach without condylar resection, using meticulous microsurgical techniques.
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OBJECTIVE: It was to observe whether a microsurgical gross total removal (GTR) of a parasagittal meningioma (PSM) outside the sinus is a safe and efficient procedure. METHOD: We identify 58 parasagittal meningiomas patients. Medical charts, operative reports, imaging studies and clinical follow-up evaluations were reviewed. RESULTS: GTR of the mass was achieved in 45 (77.7%) instances. The surgical mortality rate was 1.7%. The median follow-up time was 63 months. CONCLUSION: The surgical approach used in this group of patients afford that the great majority of tumors could be totally removed with low mortality, proving to be safe and effective.
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Senos Craneales/cirugía , Meningioma/cirugía , Microdisección/métodos , Adulto , Anciano , Anciano de 80 o más Años , Métodos Epidemiológicos , Femenino , Humanos , Imagen por Resonancia Magnética , Masculino , Meningioma/mortalidad , Meningioma/patología , Microdisección/mortalidad , Persona de Mediana Edad , Recurrencia , Factores de Tiempo , Resultado del Tratamiento , Adulto JovenRESUMEN
Objective: It was to observe whether a microsurgical gross total removal (GTR) of a parasagittal meningioma (PSM) outside the sinus is a safe and efficient procedure. Method: We identify 58 parasagittal meningiomas patients. Medical charts, operative reports, imaging studies and clinical follow-up evaluations were reviewed. Results: GTR of the mass was achieved in 45 (77.7%) instances. The surgical mortality rate was 1.7%. The median follow-up time was 63 months. Conclusion: The surgical approach used in this group of patients afford that the great majority of tumors could be totally removed with low mortality, proving to be safe and effective. .
Objetivo: Foi observar se a ressecção microcirúrgica extrassinusal dos meningiomas parasagitais é uma técnica segura e efetiva. Método: Foram estudados 58 pacientes portadores de meningiomas parasagitais. Quadros médicos, relatórios de operações, exames de imagem e seguimento clínico foram revisados. Resultados: A remoção total da lesão, fora do seio, ocorreu em 45 casos (77,7%). A taxa de mortalidade cirúrgica observada nesta série foi de 1,7%. O tempo médio de seguimento foi de 63 meses. Conclusão: A estratégia microcirúrgica empregada propiciou a remoção total dos meningiomas na maioria dos pacientes, com baixa mortalidade e morbidade, mostrando ser segura e efetiva. .
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Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Senos Craneales/cirugía , Meningioma/cirugía , Microdisección/métodos , Métodos Epidemiológicos , Imagen por Resonancia Magnética , Meningioma/mortalidad , Meningioma/patología , Microdisección/mortalidad , Recurrencia , Factores de Tiempo , Resultado del TratamientoRESUMEN
BACKGROUND: To compare the survival of glioblastoma multiforme (GBM) patients operated on at public hospital with that of patients operated on at the private hospitals. METHOD: We carried out a retrospective analysis of the patients' medical records, the surgical reports and the pre- and post-operative images of patients with a histopathological confirmed adult supratentorial GBM. Sixty-three patients were treated at public hospital and twenty-one at private hospitals. RESULTS: The present study revealed that the survival of patients treated in private hospitals was statistically superior to that of patients treated in public hospitals (11.9 vs. 7.7). CONCLUSIONS: Our study advances towards the confirmation of the hypothesis that socioeconomic and educational factors influence the Karnofsky Performance Score (KPS) and the performance of radiotherapy treatment, with negative effects over the GBM patients' survival.
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Glioblastoma/mortalidad , Neoplasias Supratentoriales/mortalidad , Adulto , Anciano , Anciano de 80 o más Años , Escolaridad , Femenino , Glioblastoma/radioterapia , Glioblastoma/cirugía , Hospitalización , Hospitales Privados , Hospitales Públicos , Humanos , Estimación de Kaplan-Meier , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Factores Socioeconómicos , Neoplasias Supratentoriales/radioterapia , Neoplasias Supratentoriales/cirugía , Adulto JovenRESUMEN
Objetivos: O glioblastoma multiforme (GBM) é a neoplasia de mais alto grau de malignidade no grupo dos tumores astrocíticos.No adulto, é o tumor primário do sistema nervoso central (SNC) mais freqüente. O objetivo do atual estudo foi observar se os fatores prognóstico do GBM como a idade, o Karnofski Performance Status (KPS), a extensão da remoção tumoral, a realização de radioterapia, o volume tumoral, e a duração dos sintomas influenciaram a sobrevida dos pacientes.Métodos: Realizamos uma revisão retrospectiva dos prontuários dos pacientes operados no Hospital Servidores do Estado doRio de Janeiro no período de 1986 a 2008.Resultados: Observamos que a idade, a realização da radioterapia e o KPS influenciaram a sobrevida dos pacientes. As demais variáveis não tiveram implicações prognósticas.Conclusão: Apesar de inúmeras pesquisas, a sobrevida dos GBM praticamente não se alterou nos últimos 30 anos, permanecendo como um desafio terapêutico. A ressecção cirúrgica complementada com radioterapia ainda é o tratamento de escolha. O papel de cada variável no prognóstico dos pacientes ainda está por ser definida nas análises multivariadas.
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Glioblastoma , Glioma , Pronóstico , SobrevidaRESUMEN
Objective: Of this study is identifying the clinical manifestations, discuss the etiology, and present the surgical treatment nuances and outcomes of patients with sub dural arachnoidal cysts (AC). Method: A retrospective study was carried out with 7 consecutives patients with spinal cord subdural AC, diagnosed, evaluated and operated at the Neurosurgical department of Servidores do Estado Hospital, from 1996 to 2010. The radiological studies, patient records, surgical descriptions and surgical videos, were reviewed, creating a database from which information was collected. The follow-up varied from 2 to 168 months (mean, 48 months). All cysts were histopathological verified. Results: Five AC were located on the thoracic spinal cord, one were located anterior in the cervical region, and one at the lumbar spinal level. The complete resection of the cyst was performed in 4 surgeries. Three patients had cysts located ventral to the cord, which precluded complete excision. The symptoms in four patients demonstrated major improvement. There was no operative death in this series, there was no major complications related to surgery. Conclusion: AC should be considered in the differential diagnosis of lesions causing myelopathy and/or a radicular pain syndrome. Microsurgical resection or generous fenestration in cysts effectively ameliorated patients' symptomatology.
Objetivo: Identificar as manifestações clínicas, discutir a etiologia, apresentar as opções terapêuticas e revelar os resultados de uma série de pacientes diagnosticados com cisto aracnoide medular subdural (CA). Método: Realizamos um estudo retrospectivo em que analisamos 7 pacientes com AC que foram operados no Hospital dos Servidores do Estado, entre 1996 e 2010. Os estudos de imagem, prontuários, descrições cirúrgicas e os vídeos foram analisados e os dados, coletados. O seguimento variou de 8 a 168 meses. Em todos os cistos foi realizado estudo histopatológico. Resultados: Cinco cistos se localizavam na medula torácica, um na cervical anterior e outro no segmento lombar. Obtivemos a excisão completa dos cistos em 4 pacientes, que apresentaram importante melhora dos sintomas. Não ocorreu nenhum óbito nessa série, nem piora do sintomas pré-operatórios. Conclusão: O CA deve ser considerado no diagnóstico diferencial das lesões que causam mielopatia ou síndrome radicular. A ressecção microcirúrgica ou uma ampla fenestração das paredes do cisto geralmente revertem os sintomas do pacientes.
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Humanos , Masculino , Femenino , Niño , Adolescente , Adulto , Quistes Aracnoideos/cirugía , Quistes Aracnoideos/etiología , Compresión de la Médula Espinal , Mielitis , CiáticaRESUMEN
Objective: Observe whether the suboccipital foramen magno decompression, duraplasty and microsurgery lyses of arachninodal bands are a safe and an effective treatment. Method: A retrospective study was carried out with 26 consecutives patients with CM1 malformations diagnosed, evaluated and operated at the Neurosurgical department of Servidores do Estado Hospital (HSE), from 1986 to 2010. The radiological studies, patient records, surgical descriptions, and when available, surgical videos, were reviewed, creating a database from which information pertinent to the present study was collected. The follow-up varied from 8 to 168 months (mean, 48 months). Results: Twenty-six patients underwent posterior fossa decompression with duraplasty. In this series, there is no operative death. We noticed beneficial outcome in 69.2% of patients, and 4 cases of transient postoperative complications. Conclusion: This experience with 26 cases CM1 proved that suboccipital craniectomy; duraplasty with autologus pericranium and microlysis of adhesions is a safe and effective procedure.
Objetivo: Observar se a descompressão cirúrgica do forâmen magno associada à duroplastia é um procedimento seguro e eficaz para o tratamento da malformação de Arnold-Chiari tipo 1. Método: Realizaram-se revisão retrospectiva dos prontuários, descrições cirúrgicas e imagens de 26 pacientes com malformação de Arnold-Chiari 1 operados no Hospital dos Servidores do Estado (HSE) no período entre 1996 e 2010. Resultados: O tratamento em 18 pacientes (68%) constitui-se de craniectomia suboccipital, remoção do arco posterior de C1 e duroplastia. Os mesmos procedimentos foram acrescidos de laminectomia de C2 em 8 indivíduos (32%). Nesta série, não ocorreu nenhum óbito cirúrgico e observou-se melhora sintomática em 68% dos pacientes. Conclusão: A craniotomia occipital com a remoção do arco de C1 e/ou laminectomia de C2 e duroplastia mostrou-se eficaz, com baixa morbidade e sem mortalidade.
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Humanos , Masculino , Femenino , Preescolar , Niño , Adolescente , Adulto Joven , Persona de Mediana Edad , Craniectomía Descompresiva , Malformación de Arnold-Chiari/cirugía , Malformación de Arnold-Chiari/fisiopatología , SiringomieliaRESUMEN
OBJECTIVE: To observe whether microsurgical removal of medullary lipomas and untethering of the medulla is a safe and efficient procedure. METHOD: A retrospective study was carried out on 38 patients with medullary lipomas associated with spinal dysraphism who underwent operations between January 1986 and January 2008, at the Neurosurgery Department of the Federal Hospital for State Public Servants, in Rio de Janeiro. RESULTS: No deaths occurred in this series, and there was no worsening of motor or bladder function among the patients. Seven individuals presented improvements in their motor deficit. Nine patients presented improvements in bladder function. Three individuals with trophic lesions achieved wound healing. CONCLUSION: Microsurgical removal of medullary lipomas associated with spinal dysraphism proved to be a safe procedure without deaths and with a low morbidity rate, and several patients achieved improvements in their neurological symptoms.