Bilateral Idiopathic Carpal Tunnel Syndrome: Clinical-Functional Characterization and Efficacy of Two Combined Postoperative Physiotherapeutic Treatments.

OBJECTIVE: To evaluate the efficacy of combined association instrument myofascial mobilization (IASTM) and stretching in patients with idiopathic bilateral carpal tunnel syndrome (CTS) operated on one hand and to analyze the response of the operated (OH) and non-operated (NH) hand according to the sequence of therapies. Research on these parameters has not yet been found in the literature. METHODS: Randomized controlled crossover study with 43 participants using the objective and subjective outcome variables. Patients were randomly assigned to two groups: starting with stretching followed by IASTM and starting with IASTM followed by stretching. Then patients underwent surgery on the hand with more severe involvement and physical therapy rehabilitation was started 30 days after for a period of 4 weeks. After the 1-week interval the participants who started with stretching were referred to IASTM and vice versa, following the same previous patterns. The outpatient reassessments took place at 3 to 6 months. Crossover ANOVA and effect sizes were used as analysis methods. RESULTS: Time was the most significant outcome for all variables both during therapies and at 6-month follow-up. Regarding response to the combined therapies between OH and NH, there were differences for both OH and NH, with the greatest impact on NH for the palmar grip and VAS variables. The treatment sequences were significant for pain on the NH and mental SF-12, suggesting that starting with IASTM followed by stretching had a superior outcome for these outcomes. CONCLUSION: The combination of IASTM with stretching, used in the postoperative period of bilateral idiopathic CTS, proved to be supplementary, with significant results and large effect sizes for most of the outcomes assessed, both during the time of application of the therapies and in the 6-month follow-up for both hands, and may constitute a viable therapeutic alternative for this population.

Neuroparacoccidioidomycosis: Case Report and Literature Review

Introduction Paracoccidioidomycosis (PCM) is a systemic mycosis caused by the fungus Paracoccidioides brasiliensis, and it can compromise the central nervous system (CNS) in 10­27% of all cases. Case Report A 31-year-old man presented to the Emergency Department with headache, left-sided weakness, clonus at the ankle and a positive Babinski sign. Head computed tomography (CT) and magnetic resonance imaging (MRI) scans showed a 5.1 3.8 cm lobulated lesion with areas of liquefaction in the right centrum semiovale. Discussion Central nervous system PCM can mimic a brain tumor, and most cases are diagnosed by biopsy of the lesion. The treatment includes antibiotics, but some cases require surgery. Conclusion Due to high morbimortality rates, the diagnosis must be considered, and early treatment started in patients who live in rural regions endemic for PCM when a ring-enhancing mass associated with perilesional edema is observed on MRI scans.

Introdução Paracoccidioidomicose (PCM) é uma micose sistêmica causada pelo fungo Paracoccidioides brasiliensis e que pode comprometer o sistema nervoso central (SNC) em 10­27% dos casos. Relato de caso Um homem de 31 anos é admitido no pronto socorro com cefaleia, hemiparesia esquerda com clonus e presença de sinal de Babinski. As imagens da tomografia computadorizada (TC) de crânio e da ressonância nuclear magnética (RNM) demonstraram uma lesão de 5,1 3,8 cm no centro semioval direito de aspecto lobulado com áreas de liquefação no centro semioval direito. Discussão Paracoccidioidomicose do SNC pode simular um tumor cerebral, sendo a maioria dos casos diagnosticada por biopsia da lesão. O tratamento inclui antibióticos, mas alguns casos necessitam de abordagem cirúrgica. Conclusão Devido à alta morbimortalidade, o diagnóstico deve ser considerado e o tratamento precoce iniciado em pacientes que vivem em áreas rurais endêmicas para PCM e que apresentam lesão com captação anelar de contraste associada a edema perilesional nas imagens de RNM.

T1-weighted gradient-echo imaging, with and without inversion recovery, in the identification of anatomical structures on the lateral surface of the brain / T1 GRE e T1 IR GRE na identificação das estruturas anatômicas da face lateral do cérebro

Abstract Objective: To compare brain structures using volumetric magnetic resonance imaging with isotropic resolution, in T1-weighted gradient-echo (GRE) acquisition, with and without inversion recovery (IR). Materials and methods: From 30 individuals, we evaluated 120 blocks of images of the left and right cerebral hemispheres being acquired by T1 GRE and by T1 IR GRE. On the basis of the Naidich et al. method for localization of anatomical landmarks, 27 anatomical structures were divided into two categories: identifiable and inconclusive. Those two categories were used in the analyses of repeatability (intraobserver agreement) and reproducibility (interobserver agreement). McNemar's test was used in order to compare the T1 GRE and T1 IR GRE techniques. Results: There was good agreement in the intraobserver and interobserver analyses (mean kappa > 0.60). McNemar's test showed that the frequency of identifiable anatomical landmarks was slightly higher when the T1 IR GRE technique was employed than when the T1 GRE technique was employed. The difference between the two techniques was statistically significant. Conclusion: In the identification of anatomical landmarks, the T1 IR GRE technique appears to perform slightly better than does the T1 GRE technique.

Resumo Objetivo: Comparar os resultados de identificação de estruturas cerebrais utilizando imagens volumétricas isotrópicas por ressonância magnética, nas aquisições T1 GRE e T1 IR GRE. Materiais e métodos: Foram avaliados 120 blocos de imagens, de 30 indivíduos, com imagens extraídas dos hemisférios cerebrais esquerdo e direito, pelos dois métodos de aquisição: T1 GRE e T1 IR GRE. Com base no método de Naidich et al. para localização dos referenciais anatômicos, 27 estruturas anatômicas foram classificadas em duas categorias - identificável versus deixam dúvidas quanto à identificação somadas às não identificáveis - para análises de repetitividade (intraobservador) e reprodutibilidade (interobservadores). Foi utilizado o teste de McNemar para a avaliação do desempenho entre os dois métodos. Resultados: Após confirmação de ter havido boa concordância na análise intraobservador e interobservadores (kappa médio > 0,60), a avaliação das imagens de cada referencial anatômico, testada entre T1 GRE e T1 IR GRE pelo teste de McNemar, indicou maior frequência de referenciais identificáveis pelo método T1 IR GRE do que pelo método T1 GRE. Conclusão: O método de imagem T1 IR GRE apresentou desempenho levemente superior, porém estatisticamente significante, em relação ao método T1 GRE, na identificação dos referenciais anatômicos cerebrais.

Evolução cronológica do conhecimento neuroanatômico / Chronological evolution of neuroanatomical knowledge

Desde a antiguidade, o pensamento científico evoluiu em fases e este artigo faz uma análise histórica sucinta sobre o avanço do conhecimento neuroanatômico. Assim, foi feita uma análise temporal que não somente permite uma descrição dessa evolução, bem como esclarece o modo e a profundidade com que as estruturas foram sendo compreendidas. A descrição das descobertas neuroanatômicas subdividida em quatro fases temporais distintas permitiu compreender a evolução do pensamento neurológico e as correlações existentes entre os relatos.

Since ancient times, the scientific thinking evolved in stages, and thisarticle is a brief historical analysis of the progress of the neuroanatomical knowledge. Consequently, a temporal analysis not only provides a description of this evolution, as explained by the manner and depth with which the structures were being understood. The description of the neuroanatomical finfings subdivided into four distinct temporal phases allowed to understand the evolution of neurological thought and the correlations between the reports.

T1-weighted gradient-echo imaging, with and without inversion recovery, in the identification of anatomical structures on the lateral surface of the brain.

OBJECTIVE: To compare brain structures using volumetric magnetic resonance imaging with isotropic resolution, in T1-weighted gradient-echo (GRE) acquisition, with and without inversion recovery (IR). MATERIALS AND METHODS: From 30 individuals, we evaluated 120 blocks of images of the left and right cerebral hemispheres being acquired by T1 GRE and by T1 IR GRE. On the basis of the Naidich et al. method for localization of anatomical landmarks, 27 anatomical structures were divided into two categories: identifiable and inconclusive. Those two categories were used in the analyses of repeatability (intraobserver agreement) and reproducibility (interobserver agreement). McNemar's test was used in order to compare the T1 GRE and T1 IR GRE techniques. RESULTS: There was good agreement in the intraobserver and interobserver analyses (mean kappa > 0.60). McNemar's test showed that the frequency of identifiable anatomical landmarks was slightly higher when the T1 IR GRE technique was employed than when the T1 GRE technique was employed. The difference between the two techniques was statistically significant. CONCLUSION: In the identification of anatomical landmarks, the T1 IR GRE technique appears to perform slightly better than does the T1 GRE technique.

OBJETIVO: Comparar os resultados de identificação de estruturas cerebrais utilizando imagens volumétricas isotrópicas por ressonância magnética, nas aquisições T1 GRE e T1 IR GRE. MATERIAIS E MÉTODOS: Foram avaliados 120 blocos de imagens, de 30 indivíduos, com imagens extraídas dos hemisférios cerebrais esquerdo e direito, pelos dois métodos de aquisição: T1 GRE e T1 IR GRE. Com base no método de Naidich et al. para localização dos referenciais anatômicos, 27 estruturas anatômicas foram classificadas em duas categorias - identificável versus deixam dúvidas quanto à identificação somadas às não identificáveis - para análises de repetitividade (intraobservador) e reprodutibilidade (interobservadores). Foi utilizado o teste de McNemar para a avaliação do desempenho entre os dois métodos. RESULTADOS: Após confirmação de ter havido boa concordância na análise intraobservador e interobservadores (kappa médio > 0,60), a avaliação das imagens de cada referencial anatômico, testada entre T1 GRE e T1 IR GRE pelo teste de McNemar, indicou maior frequência de referenciais identificáveis pelo método T1 IR GRE do que pelo método T1 GRE. CONCLUSÃO: O método de imagem T1 IR GRE apresentou desempenho levemente superior, porém estatisticamente significante, em relação ao método T1 GRE, na identificação dos referenciais anatômicos cerebrais.

Displasia fibrosa óssea extensa em coluna cervical de paciente jovem e assintomático: Relato de caso / Extense cervical fibrous dysplasia of bones in young Assymptomatic Patient. Case Report

Introdução: A Displasia Fibrosa Óssea (DFO) é uma lesão benigna, representando 5 a 7% dos tumores ósseos benignos. Temsua etiologia relacionada a mutações somáticas. Classifica-se em monostótica, quando atinge apenas um osso ou poliostóticano envolvimento de mais de um. O acometimento cervical é raro, sendo mais comum na apresentação poliostótica. Os casoscom comprometimento funcional ou estético excessivo constituem-se como principais indicações para o tratamento cirúrgico.Objetivos: Os autores mostram o tratamento da lesão destrutiva do corpo vertebral cervical, quinto segmento, causada porDFO monostótica, por meio de somatectomia associada a artrodese anterior com substituto de corpo vertebral, placa detitânio anterior, laminectomia e fixação posterior com cabos de titânio sublaminares. Métodos e Resultados: Relato de caso,inicialmente de trauma automobilístico, que após estudo por imagem da coluna cervical confirmou diagnóstico de DFO. Devidoà instabilidade da região cervical indicou-se cirurgia, sobre a qual foram comentadas suas principais etapas...

Introduction: Fibrous Dysplasia of bones (FDB) is a benign lesion, representing 5-7% of all benign bone tumors. Its etiology isassociated to somatic mutations. It is classified as monostotic only when it reaches a bone, polyostotic when there is involvementof two or more bones. The cervical involvement is rare and is more common in polyostotic presentation. Cases with excessivefunctional or aesthetic impairment constitute the main indications for surgical treatment. Objectives: The authors present thetreatment of destructive lesions of the cervical vertebral body, segment of the fifth vertebra, caused by FDB monostotic usingsomatectomia associated to anterior arthrodesis with vertebral body replacement, titanium plate anterior, laminectomy andposterior fixation with sublaminares tittanium system. Methods and Results: Initially detected as an automobile trauma, afterimaging study of the cervical spine confirmed diagnosis of FDB. Due to the instability of the cervical region, surgery wasindicated...

Brainstem cavernomas: a surgical challenge.

OBJECTIVE: The authors show their experience with brainstem cavernomas, comparing their data with the ones of a literature review. METHODS: From 1998 to 2009, 13 patients harboring brainstem cavernomas underwent surgical resection. All plain films, medical records and images were reviewed in order to sample the most important data regarding epidemiology, clinical picture, radiological findings and surgical outcomes, as well as main complications. RESULTS: The mean age was 42.4 years (ranging from 19 to 70). No predominant gender: male-to-female ratio, 6:7. Pontine cases were more frequent. Magnetic resonance imaging was used as the imaging method to diagnose cavernomas in all cases. The mean follow-up was 71.3 months (range of 1 to 138 months). Clinical presentation was a single cranial nerve deficit, VIII paresis, tinnitus and hearing loss (69.2%). All 13 patients underwent resection of the symptomatic brainstem cavernoma. Complete removal was accomplished in 11 patients. Morbidity and mortality were 15.3 and 7.6%, respectively. CONCLUSIONS: Cavernomas can be resected safely with optimal surgical approach (feasible entry zone) and microsurgical techniques, and the goal is to remove all lesions with no cranial nerves impairment.

Brainstem cavernomas: a surgical challenge / Cavernomas de tronco: desafio cirúrgico

Objective: The authors show their experience with brainstem cavernomas, comparing their data with the ones of a literature review. Methods: From 1998 to 2009, 13 patients harboring brainstem cavernomas underwent surgical resection. All plain films, medical records and images were reviewed in order to sample the most important data regarding epidemiology, clinical picture, radiological findings and surgical outcomes, as well as main complications. Results: The mean age was 42.4 years (ranging from 19 to 70). No predominant gender: male-to-female ratio, 6:7. Pontine cases were more frequent. Magnetic resonance imaging was used as the imaging method to diagnose cavernomas in all cases. The mean follow-up was 71.3 months (range of 1 to 138 months). Clinical presentation was a single cranial nerve deficit, VIII paresis, tinnitus and hearing loss (69.2%). All 13 patients underwent resection of the symptomatic brainstem cavernoma. Complete removal was accomplished in 11 patients. Morbidity and mortality were 15.3 and 7.6%, respectively. Conclusions: Cavernomas can be resected safely with optimal surgical approach (feasible entry zone) and microsurgical techniques, and the goal is to remove all lesions with no cranial nerves impairment.

Objetivo: Os autores mostram sua experiência com cavernomas de tronco cerebral, comparando seus dados com os de uma revisão da literatura. Métodos: De 1998 a 2009, 13 pacientes com cavernoma de tronco cerebral foram submetidos a ressecção cirúrgica. Todos os filmes, prontuários e imagens foram revisados para exposição dos dados mais importantes, como epidemiologia, detalhes clínicos, achados radiológicos e resultados cirúrgicos, bem como as principais complicações. Resultados: A média de idade foi de 42,4 anos (variação de 19 a 70). Não houve predominância de gênero na taxa masculino versus feminino, 6:7. Os casos pontinos foram os mais frequentes. Ressonância nuclear magnética foi o método de imagem para o diagnóstico de cavernomas em todos os casos. A média do acompanhamento foi de 71,3 meses (variação de 1 a 138 meses). A apresentação clínica mais frequente foi a paresia do VIII nervo craniano, tinitus e perda auditiva (69,2%). Todos os 13 pacientes com cavernomas de tronco sintomáticos foram submetidos à ressecção cirúrgica. A remoção total foi realizada em 11 pacientes. A morbidade e a mortalidade foram de 15,3 e 7,6%, respectivamente. Conclusão: Os cavernomas podem ser seguramente ressecados por meio de acessos cirúrgicos ideais (zonas de entrada seguras) e técnicas de microcirurgia, sendo que o objetivo é remover toda a lesão sem o comprometimento dos nervos cranianos.

O papel do tratamento medicamentoso no traumatismo crâni encefálic: um novo conceito / The role of drug management in traumatic brain injury: a new concept

O traumatismo crânio-encefálico (TCE) é a maior causa de morbidade e mortalidade, acometendo particularmente a população jovem. Através do entendimento do conceito de lesão celular, tratamentos atuais mostram avanços medicamentosos que atuam na cascata secundária do TCE. Os autores mostram um estudo de revisão sobre os benefícios do uso da progesterona, citocolina, fator VII recombinante, endotelina, ciclosporina e amantadina no tratamento do TCE.

Traumatic brain injury (TBI) is a major cause of morbidity andmortality, particularly among young people. Understandingthe concept of cellular injury, the current management showsadvances in medical treatment in the secondary cascadeof TBI. The authors show a review study concerning to thepossible benefit of progesterone, citocholine, activatedrecombinant factor VII , endothelin, ciclosporin, amantadinein TBI treatment.

Genetic polymorphisms associated with the development and clinical course of multiple sclerosis (review).

Multiple sclerosis (MS) is an autoimmune disease characterized by areas of inflammation, demyelination and axonal damage. The etiology of MS is multifactorial with an interaction between genetic, environmental and geographical factors. The objective of this study was to review the physiopathology and the genetic polymorphisms associated with the development and clinical course of MS. Studies carried out in populations worldwide showed that polymorphisms in the genes of the major histocompatibility complex (MHC) class II and class III have been associated with susceptibility, resistance and clinical forms of MS. Considerable attention has been focused on studies evaluating disease-modifying effects in MS that identified seven genes of probable importance such as the HLA class II, ApoE, IL-1ra, IL-1ß, TNF-α, TNF-ß and CCR5 genes. However, the results described in the literature about genetic biomarkers in MS are not consistent in the worldwide population. The detection of a single nucleotide polymorphism involved in the etiology and physiopathology of MS is very difficult and, it is likely that, several genetic polymorphisms are involved, each with a small contribution to the susceptibility or resistance to MS. Taken together the results show the need for continued research in genetically heterogeneous populations to identify new biomarkers associated with MS that could be used as prognostic markers or as therapeutic targets to modulate the autoimmune response in MS patients. This information may contribute to a better understanding of the physiopathology and treatment of MS, with the possibility of developing different therapeutic strategies according to the genetic profile of each individual.