WAGNER CID PALMEIRA CAVALCANTE

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Projetos de Pesquisa
Unidades Organizacionais
LIM/45 - Laboratório de Fisiopatologia Neurocirúrgica, Hospital das Clínicas, Faculdade de Medicina

Resultados de Busca

Agora exibindo 1 - 10 de 13
  • article 0 Citação(ões) na Scopus
    Radiologic and histologic findings in Sjogren's sensory neuronopathy
    (2019) GRATIVVOL, Ronnyson Susano; CAVALCANTE, Wagner Cid Palmeira; VENTURA, Lais Maria Gomes de Brito; CALDAS, Vitor Marques; LUCATO, Leandro Tavares; LOURENCO, Silvia Vanessa; HEISE, Carlos Otto; NITRINI, Ricardo
  • article 14 Citação(ões) na Scopus
    MUSCULOSKELETAL ULTRASOUND IN INCLUSION BODY MYOSITIS: A COMPARATIVE STUDY WITH MAGNETIC RESONANCE IMAGING
    (2021) GUIMARAES, Julio Brandao; CAVALCANTE, Wagner Cid Palmeira; CRUZ, Isabela A. N.; NICO, Marcelo A.; ORMOND FILHO, Alipio G.; SILVA, Andre M. Serafim Da; ZANOTELI, Edmar
    objective of this study was to compare the accuracy of ultrasound (US) with that of magnetic resonance imaging (MRI) in identifying muscle abnormalities in patients with inclusion body myositis (IBM). Twelve patients with IBM underwent muscle US and MRI on the same day. Twelve muscle groups were analyzed per patient. On US, a visual grading system was used to detect whether the muscles were affected. On MRI, muscle atrophy, fat infiltration and edema patterns were analyzed. The inter- and intra-reader reproducibility was similar for US and MRI in the evaluation of muscle abnormalities. All patients with muscle abnormalities identified on US presented with fat infiltration on MRI, which was the most common abnormality identified on MRI. Most importantly, the accuracy of US compared with that of MRI for the detection of muscle abnormalities in patients with IBM was 86.8 (K coefficient = 0.632), with a sensitivity of 84% and specificity of 100%. In conclusion all patients with muscle abnormalities identified on US presented with fat infiltration on MRI, and the marked increase in echo intensity observed in the muscles of IBM patients was related mostly to fatty replacement. Most importantly, US exhibited significant accuracy compared with MRI. (E-mail: julio.guimaraes@grupofleury.com. br) (c) 2021 World Federation for Ultrasound in Medicine & Biology. All rights reserved.
  • article 14 Citação(ões) na Scopus
    The importance of recognizing faciobrachial dystonic seizures in rapidly progressive dementias
    (2016) SIMABUKURO, Mateus Mistieri; NÓBREGA, Paulo Ribeiro; PITOMBEIRA, Milena; CAVALCANTE, Wagner Cid Palmeira; GRATIVVOL, Ronnyson Susano; PINTO, Lécio Figueira; CASTRO, Luiz Henrique Martins; NITRINI, Ricardo
    ABSTRACT Background: Creutzfeldt-Jakob Disease (CJD) is the prototypical cause of rapidly progressive dementia (RPD). Nonetheless, efforts to exclude reversible causes of RPD that mimic prion disease are imperative. The recent expanding characterization of neurological syndromes associated with antibodies directed against neuronal cell surface or sympathic antigens, namely autoimmune encephalitis is shifting paradigms in neurology. Such antigens are well known proteins and receptors involved in synaptic transmission. Their dysfunction results in neuropsychiatric symptoms, psychosis, seizures, movement disorders and RPD. Faciobrachial dystonic seizure (FBDS) is a novel characterized type of seizure, specific for anti-LGI1 encephalitis. Objective: In order to improve clinical recognition we report the cases of two Brazilian patients who presented with characteristic FDBS (illustrated by videos) and anti-LGI1 encephalitis. Methods: We have included all patients with FBDS and confirmed anti-LGI1 encephalitis and video records of FDBS in two tertiary Brazilian centers: Department of Neurology of Hospital das Clínicas, Sao Paulo University, Sao Paulo, Brazil and Hospital Geral de Fortaleza, Fortaleza, Brazil between January 1, 2011 and December 31, 2015. Results: Both patients presented with clinical features of limbic encephalitis associated with FBDS, hyponatremia and normal CSF. None of them presented with tumor and both showed a good response after immunotherapy. Conclusion: FBDSs may be confounded with myoclonus and occurs simultaneously with rapid cognitive decline. Unawareness of FDBS may induce to misdiagnosing a treatable cause of RPD as CJD.
  • bookPart
    Síndromes neurovasculares
    (2021) CAVALCANTE, Wagner Cid Palmeira; GRATIVVOL, Ronnyson Susano
  • article 1 Citação(ões) na Scopus
    Unilateral abdominal protrusion as the main diagnostic sign of facioscapulohumeral dystrophy
    (2019) SILVA, Andre Macedo Serafim da; CAVALCANTE, Wagner Cid Palmeira; CAMELO, Clara Gontijo; MENDONCA, Rodrigo de Holanda; FORTINI, Ida; CARVALHO, Mary Souza de; ZANOTELI, Edmar
  • bookPart
    Eletroneuromiografia: o que o neurologista geral deve saber?
    (2020) CAVALCANTE, Wagner Cid Palmeira; GRATIVVOL, Ronnyson Susano; HEISE, Carlos Otto
  • article 14 Citação(ões) na Scopus
    Selective visuoconstructional impairment following mild COVID-19 with inflammatory and neuroimaging correlation findings
    (2023) PAULA, Jonas Jardim de; PAIVA, Rachel E. R. P.; SOUZA-SILVA, Nathalia Gualberto; ROSA, Daniela Valadao; DURAN, Fabio Luis de Souza; COIMBRA, Roney Santos; COSTA, Danielle de Souza; DUTENHEFNER, Pedro Robles; OLIVEIRA, Henrique Soares Dutra; CAMARGOS, Sarah Teixeira; VASCONCELOS, Herika Martins Mendes; CARVALHO, Nara de Oliveira; SILVA, Juliana Batista da; SILVEIRA, Marina Bicalho; MALAMUT, Carlos; OLIVEIRA, Derick Matheus; MOLINARI, Luiz Carlos; OLIVEIRA, Danilo Bretas de; JANUARIO, Jose Nelio; SILVA, Luciana Costa; MARCO, Luiz Armando De; QUEIROZ, Dulciene Maria de Magalhaes; MEIRA, Wagner; BUSATTO, Geraldo; MIRANDA, Debora Marques; ROMANO-SILVA, Marco Aurelio
    People recovered from COVID-19 may still present complications including respiratory and neurological sequelae. In other viral infections, cognitive impairment occurs due to brain damage or dysfunction caused by vascular lesions and inflammatory processes. Persistent cognitive impairment compromises daily activities and psychosocial adaptation. Some level of neurological and psychiatric consequences were expected and described in severe cases of COVID-19. However, it is debatable whether neuropsychiatric complications are related to COVID-19 or to unfoldings from a severe infection. Nevertheless, the majority of cases recorded worldwide were mild to moderate self-limited illness in non-hospitalized people. Thus, it is important to understand what are the implications of mild COVID-19, which is the largest and understudied pool of COVID-19 cases. We aimed to investigate adults at least four months after recovering from mild COVID-19, which were assessed by neuropsychological, ocular and neurological tests, immune markers assay, and by structural MRI and (18)FDG-PET neuroimaging to shed light on putative brain changes and clinical correlations. In approximately one-quarter of mild-COVID-19 individuals, we detected a specific visuoconstructive deficit, which was associated with changes in molecular and structural brain imaging, and correlated with upregulation of peripheral immune markers. Our findings provide evidence of neuroinflammatory burden causing cognitive deficit, in an already large and growing fraction of the world population. While living with a multitude of mild COVID-19 cases, action is required for a more comprehensive assessment and follow-up of the cognitive impairment, allowing to better understand symptom persistence and the necessity of rehabilitation of the affected individuals.
  • article 2 Citação(ões) na Scopus
    Effect of the COVID-19 pandemic on patients with inherited neuromuscular disorders
    (2022) MORENO, Cristiane Araujo Martins; CAMELO, Clara Gontijo; SAMPAIO, Pedro Henrique Marte de Arruda; FONSECA, Alulin Tacio Quadros Santos Monteiro; ESTEPHAN, Eduardo de Paula; SILVA, Andre Macedo Serafim; PIROLA, Renann Nunes; SILVA, Luiz Henrique Libardi; LIMA, Karlla Danielle Ferreira; ALBUQUERQUE, Marco Antonio Veloso de; CAMELO FILHO, Antonio Edvan; MARQUES, Marcos Vinicius Oliveira; YANAGIURA, Mario Teruo; CAVALCANTE, Wagner Cid Palmeira; MATSUI JUNIOR, Ciro; ISIHI, Lucas Michielon de Augusto; MENDONCA, Rodrigo Holanda; POUZA, Ana Flavia Pincerno; CARVALHO, Mary Souza de; REED, Umbertina Conti; ZANOTELI, Edmar
    Background: The COVID-19 pandemic has brought substantial challenges for current practices in treating hereditary neuromuscular disorders (hNMDs). However, this infection has not been the only concern for these patients. Social distancing has compromised multidisciplinary assistance and physical activity, and has brought about several mental health issues. We presented a follow-up on 363 patients with hNMDs at a Brazilian tertiary center during the peak of the COVID-19 pandemic. Objective: We aimed to show the frequency and severity of SARS-CoV-2 infection among hNMD patients and to demonstrate the effects of the pandemic on life habits, disease progression and multidisciplinary supportive care status. Methods:Three hundred and sixty-three patients (58% male and 42% female) were followed for three months through three teleconsultations during the peak of the COVID-19 pandemic in Brazil. Results: There were decreases in the numbers of patients who underwent physical, respiratory and speech therapies. For several patients, their appetite (33%) and sleep habits (25%) changed. Physical exercises and therapies were interrupted for most of the patients. They reported new onset/worsening of fatigue (17%), pain (17%), contractions (14%) and scoliosis (7%). Irritability and sleep, weight and appetite changes, and especially diminished appetite and weight loss, were more frequent in the group that reported disease worsening. There was a low COVID-19 contamination rate (0.8%), and all infected patients had a mild presentation. Conclusion: The isolation by itself was protective from a COVID-19 infection perspective. However, this isolation might also trigger a complex scenario with life habit changes that are associated with an unfavorable course for the NMD.
  • article 1 Citação(ões) na Scopus
    Teaching NeuroImages: Bilateral intracerebral hemorrhage in expanded dengue syndrome
    (2017) CAVALCANTE, Wagner Cid Palmeira; SOARES NETO, Herval Ribeiro; GRATIVVOL, Ronnyson Susano; SPERA, Raphael Ribeiro; FRASSETTO, Fernando Pereira; LUCATO, Leandro Tavares; NITRINI, Ricardo
  • article 0 Citação(ões) na Scopus
    Imaging findings in faciobrachial dystonic seizures associated with LGI-1 antibodies
    (2016) GRATIVVOL, Ronnyson Susano; SIMABUKURO, Mateus Mistieri; SPERA, Raphael Ribeiro; CAVALCANTE, Wagner Cid Palmeira; ARAUJO, Hugo Henrique Soares; SAKUNO, Daniel; LUCATO, Leandro Tavares; PINTO, Lecio Figueira; CASTRO, Luiz Henrique Martins; NITRINI, Ricardo