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1.
Acta Neurochir (Wien) ; 163(10): 2931-2939, 2021 10.
Artigo em Inglês | MEDLINE | ID: mdl-34387743

RESUMO

BACKGROUND: Early cranioplasty has been encouraged after decompressive craniectomy (DC), aiming to reduce consequences of atmospheric pressure over the opened skull. However, this practice may not be often available in low-middle-income countries (LMICs). We evaluated clinical improvement, hemodynamic changes in each hemisphere, and the hemodynamic balance between hemispheres after late cranioplasty in a LMIC, as the institution's routine resources allowed. METHODS: Prospective cohort study included patients with bone defects after DC evaluated with perfusion tomography (PCT) and transcranial Doppler (TCD) and performed neurological examinations with prognostic scales (mRS, MMSE, and Barthel Index) before and 6 months after surgery. RESULTS: A final sample of 26 patients was analyzed. Satisfactory improvement of neurological outcome was observed, as well as significant improvement in the mRS (p = 0.005), MMSE (p < 0.001), and Barthel Index (p = 0.002). Outpatient waiting time for cranioplasty was 15.23 (SD 17.66) months. PCT showed a significant decrease in the mean transit time (MTT) and cerebral blood volume (CBV) only on the operated side. Although most previous studies have shown an increase in cerebral blood flow (CBF), we noticed a slight and nonsignificant decrease, despite a significant increase in the middle cerebral artery flow velocity in both hemispheres on TCD. There was a moderate correlation between the MTT and contralateral muscle strength (r = - 0.4; p = 0.034), as well as between TCD and neurological outcomes ipsilateral (MMSE; r = 0.54, p = 0.03) and contralateral (MRS; p = 0.031, r = - 0.48) to the operated side. CONCLUSION: Even 1 year after DC, cranioplasty may improve cerebral perfusion and neurological outcomes and should be encouraged.


Assuntos
Craniectomia Descompressiva , Procedimentos de Cirurgia Plástica , Encéfalo , Circulação Cerebrovascular , Hemodinâmica , Humanos , Estudos Prospectivos , Crânio/diagnóstico por imagem , Crânio/cirurgia , Resultado do Tratamento
2.
Int J Radiat Oncol Biol Phys ; 119(4): 1122-1132, 2024 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-38232937

RESUMO

PURPOSE: The aim of this work was to investigate whether reirradiation of recurrent glioblastoma with hypofractionated stereotactic radiation therapy (HSRT) consisting of 35 Gy in 5 fractions (35 Gy/5 fx) compared with 25 Gy in 5 fractions (25 Gy/5 fx) improves outcomes while maintaining acceptable toxicity. METHODS AND MATERIALS: We conducted a prospective randomized phase 2 trial involving patients with recurrent glioblastoma (per the 2007 and 2016 World Health Organization classification). A minimum interval from first radiation therapy of 5 months and gross tumor volume of 150 cc were required. Patients were randomized 1:1 to receive HSRT alone in 25 Gy/5 fx or 35 Gy/5 fx. The primary endpoint was progression-free survival (PFS). We used a randomized phase 2 screening design with a 2-sided α of 0.15 for the primary endpoint. RESULTS: From 2011 to 2019, 40 patients were randomized and received HSRT, with 20 patients in each group. The median age was 50 years (range, 27-71); a new resection before HSRT was performed in 75% of patients. The median PFS was 4.9 months in the 25 Gy/5 fx group and 5.2 months in the 35 Gy/5 fx group (P = .23). Six-month PFS was similar at 40% (85% CI, 24%-55%) for both groups. The median overall survival (OS) was 9.2 months in the 25 Gy/5 fx group and 10 months in the 35 Gy/5 fx group (P = .201). Grade ≥3 necrosis was numerically higher in the 35 Gy/5 fx group (3 [16%] vs 1 [5%]), but the difference was not statistically significant (P = .267). In an exploratory analysis, median OS of patients who developed treatment-related necrosis was 14.1 months, and that of patients who did not was 8.7 months (P = .003). CONCLUSIONS: HSRT alone with 35 Gy/5 fx was not superior to 25 Gy/5 fx in terms of PFS or OS. Due to a potential increase in the rate of clinically meaningful treatment-related necrosis, we suggest 25 Gy/5 fx as the standard dose in HSRT alone. During follow-up, attention should be given to differentiating tumor progression from potentially manageable complications.


Assuntos
Neoplasias Encefálicas , Glioblastoma , Recidiva Local de Neoplasia , Intervalo Livre de Progressão , Hipofracionamento da Dose de Radiação , Radiocirurgia , Reirradiação , Humanos , Glioblastoma/radioterapia , Glioblastoma/mortalidade , Glioblastoma/cirurgia , Glioblastoma/patologia , Pessoa de Meia-Idade , Idoso , Masculino , Feminino , Reirradiação/efeitos adversos , Adulto , Estudos Prospectivos , Radiocirurgia/efeitos adversos , Radiocirurgia/métodos , Recidiva Local de Neoplasia/radioterapia , Neoplasias Encefálicas/radioterapia , Neoplasias Encefálicas/mortalidade , Neoplasias Encefálicas/patologia , Neoplasias Encefálicas/cirurgia , Fracionamento da Dose de Radiação , Necrose
3.
J Comput Assist Tomogr ; 37(5): 698-700, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24045243

RESUMO

Alexander disease (AxD) is a rare neurodegenerative disorder related to mutations in the glial fibrillary acidic protein gene. We report the case of a child with disease onset at the age of 3 months and a novel mutation in the glial fibrillary acidic protein gene. Peculiar aspects were initially atypical clinical and magnetic resonance imaging (MRI) findings, which became typical during follow-up. The child was born after an uneventful pregnancy, presented initially only as a failure to thrive. The first MRI examination demonstrated obstructive hydrocephalus and cerebral white matter abnormalities (which were more prominent posteriorly). During follow-up, her clinical picture became typical of AxD with macrocephaly and neurodevelopmental delay. Sequential MRI examinations showed frontal white matter involvement, together with exuberant forniceal lesions and areas of contrast enhancement.


Assuntos
Doença de Alexander/genética , Doença de Alexander/patologia , Encéfalo/patologia , Proteína Glial Fibrilar Ácida/genética , Imageamento por Ressonância Magnética/métodos , Polimorfismo de Nucleotídeo Único/genética , Feminino , Humanos , Lactente , Mutação/genética
4.
Int Arch Otorhinolaryngol ; 21(3): 302-307, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28680502

RESUMO

Introduction Vertebrobasilar insufficiency is defined as transitory ischemia of the vertebrobasilar circulation. Dizziness, vertigo, headaches, vomit, diplopia, blindness, ataxia, imbalance, and weakness in both sides of the body are the most common symptoms. Objective To review the literature regarding the three available diagnostic testing in patients with dizziness complaints secondary to vertebrobasilar insufficiency (VBI): magnetic resonance angiography; transcranial Doppler ultrasound; and vertebrobasilar deprivation testing. Data Synthesis We selected 28 studies that complied with our selection criteria for appraisal. The most frequent cause of the hemodynamic changes leading to VBI is atherosclerosis. The main clinical symptoms are dizziness, vertigo, headaches, vomit, diplopia, blindness, ataxia, imbalance, and weakness in both sides of the body. Even though arteriography is considered the most important exam to diagnose the disease, the inherent risks of this exam should be taken into consideration. The magnetic resonance angiography has been widely studied and is a good method to identify and localize any occlusions and stenosis in both neck and intracranial great vessels. Conclusion Each patient with a suspected diagnosis of VBI should be individually evaluated and treated, taking in consideration the pros and cons of each diagnostic testing and treatment option.

5.
Int. arch. otorhinolaryngol. (Impr.) ; 21(3): 302-307, July-Sept. 2017. tab, graf
Artigo em Inglês | LILACS | ID: biblio-892802

RESUMO

Abstract Introduction Vertebrobasilar insufficiency is defined as transitory ischemia of the vertebrobasilar circulation. Dizziness, vertigo, headaches, vomit, diplopia, blindness, ataxia, imbalance, and weakness in both sides of the body are the most common symptoms. Objective To review the literature regarding the three available diagnostic testing in patients with dizziness complaints secondary to vertebrobasilar insufficiency (VBI): magnetic resonance angiography; transcranial Doppler ultrasound; and vertebrobasilar deprivation testing. Data Synthesis We selected 28 studies that complied with our selection criteria for appraisal. The most frequent cause of the hemodynamic changes leading to VBI is atherosclerosis. The main clinical symptoms are dizziness, vertigo, headaches, vomit, diplopia, blindness, ataxia, imbalance, and weakness in both sides of the body. Even though arteriography is considered the most important exam to diagnose the disease, the inherent risks of this exam should be taken into consideration. The magnetic resonance angiography has been widely studied and is a good method to identify and localize any occlusions and stenosis in both neck and intracranial great vessels. Conclusion Each patient with a suspected diagnosis of VBI should be individually evaluated and treated, taking in consideration the pros and cons of each diagnostic testing and treatment option.

7.
Rev. med. (Säo Paulo) ; 90(4): 157-168, out.-dez. 2011. ilus
Artigo em Português | LILACS | ID: lil-747300

RESUMO

A avaliação por imagem do traumatismocranioencefálico (TCE) tem tido importante papel na determinação do pronto diagnóstico de lesões traumáticas intracranianas, definindo conduta terapêutica clínica ou cirúrgica emergencial, posteriormente auxiliandona monitorização terapêutica e permitindo acesso a estimativa mais precisa do prognóstico do paciente.A tomografia computadorizada (TC) é o método por imagem mais adequado no atendimento inicial ao paciente vítima de TCE detectando rapidamente lesõespotencialmente fatais que necessitem de tratamento cirúrgico imediato. A angiotomografia permite diagnosticarlesões vasculares crânio-cervicais potencialmente graves. Após a estabilização clínica destes pacientes a ressonância magnética (RM) contribui no aumento da detecção e na melhor caracterização das lesões traumáticas encefálicas e de suas possíveis complicações tais como herniaçõescerebrais e lesões isquêmicas. Neste artigo serão abordadas as principais lesões traumáticas primárias e secundárias cranioencefálicas e suas principais características à TC e RM, métodos que fornecem importantes informações diagnósticas e prognósticas nos pacientes vítimas de TCE.


The imaging evaluation of traumatic brain injury (TBI) has played an important role in determining the early diagnosis of traumatic intracranial injury, defining therapeutic medical or surgical emergency, subsequentlyassisting in monitoring therapy and allowing access to more accurate estimate of the patient’s prognosis. Computed tomography (CT) imaging is the method most appropriate to the patient in the initial care of TBI victim quickly detecting life-threatening injuries requiring immediate surgicaltreatment. The angiotomography (CTA) allows diagnosing craniocervical vascular lesions potentially serious. After clinical stabilization of these patients magnetic resonance imaging (MRI) contributes to increased detection and better characterization of traumatic brain injuries and its possible complications such as cerebral herniation and ischemic lesions. In this article we will discuss the major primary and secondary traumatic cranioencephalic injuries and its main features on CT and MRI methods that provide important diagnostic and prognostic information in patientsvictims of TBI.


Assuntos
Diagnóstico por Imagem , Imageamento por Ressonância Magnética , Tomografia Computadorizada por Raios X , Traumatismos Craniocerebrais , Traumatismos do Sistema Nervoso , Traumatismos Craniocerebrais/diagnóstico
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