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Custo e Carga da Atrofia Muscular Espinhal em Portugal 葡萄牙脊髓肌肉萎缩的成本和费用
Q4 Medicine Pub Date : 2021-01-20 DOI: 10.46531/sinapse/ao/210058/2021
João Costa
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引用次数: 1
Refractory Post-Dural Puncture Headache: The Utility of Computed Tomography Myelography 硬脑膜穿刺后顽固性头痛:计算机断层扫描脊髓造影的应用
Q4 Medicine Pub Date : 2021-01-20 DOI: 10.46531/sinapse/cc/210049/2021
José Lourenço Rosa
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引用次数: 0
Rare Presentation of Spontaneous Carotid Artery Dissection 罕见的自发性颈动脉夹层
Q4 Medicine Pub Date : 2021-01-20 DOI: 10.46531/sinapse/in/210018/2021
Abreu Ângela
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引用次数: 0
Balo’s Concentric Sclerosis Mimicking High-Grade Tumor Balo 's同心硬化模拟高级别肿瘤
Q4 Medicine Pub Date : 2021-01-20 DOI: 10.46531/sinapse/in/210066/2021
Catarina Pinto
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引用次数: 0
Reflexões 反射
Q4 Medicine Pub Date : 2021-01-20 DOI: 10.11606/issn.2318-9800.v0i14p119-121
Catarina Resende de Oliveira
Com embasamento nos estudos feitos pelos pesquisadores Pierre Dardot e Chistian Laval, o presente artigo tece reflexões sobre o neoliberalismo configurado como uma racionalidade
本文以达多和拉瓦尔的研究为基础,对新自由主义作为一种理性进行了反思
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引用次数: 2
Pandemia COVID-19: Mitigação de uma Injustiça 新冠肺炎大流行:减轻不公正
Q4 Medicine Pub Date : 2020-07-13 DOI: 10.46531/sinapse/ed/covid19/barrosj/2020
J. Barros, Porto Portugal Centro Hospitalar Universitário do Porto
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引用次数: 0
Pediatric Miller-Fisher Syndrome: clinical features and diagnostic challenges 儿童米勒-费舍尔综合征:临床特征和诊断挑战
Q4 Medicine Pub Date : 2020-06-30 DOI: 10.46531/SINAPSE/2020/CC/190008/2020
AI Martins, Vasconcelos, Palavra
Miller-Fisher syndrome is an acute demyelinating polyneuropathy and classically presents with ophthalmoplegia, hyporeflexia, and ataxia. Although being one of the rare variants of Guillain-Barré syndrome, there are several clinical, laboratory and imaging peculiarities of Miller-Fisher syndrome inherent to patient’s age group. We present a three-year old patient, which presented with a three days-history of gait imbalance and ocular movements impairment. Neurological examination revealed complete ophthalmoplegia, appendicular and axial ataxia and hyporeflexia. Cerebrospinal fluid study revealed albuminocytologic dissociation while nerve conduction tests, brain magnetic resonance imaging and anti-ganglioside antibodies screening were unrevealing. The patient was diagnosed with Miller-Fisher syndrome and started intravenous human immunoglobulin (2 g/kg), for 5 days. Three months after the diagnosis, the patient was fully recovered and the neurological examination was unremarkable. It is crucial to recognize pediatric Miller-Fisher syndrome particularities, surpass the difficulties in performing an accurate neurological exam in young patients and recognize the multiple entities to consider n the differential diagnosis of pediatric Miller-Fisher syndrome, in order to perform a correct diagnosis and establish an appropriate therapeutic strategy. Informações/Informations: Caso Clínico, publicado em Sinapse, Volume 20, Número 1, janeiro-março 2020. Versão eletrónica em www.sinapse.pt Case Report, published in Sinapse, Volume 20, Number 1, january-march 2020. Electronic version in www.sinapse.pt © Autor (es) (ou seu (s) empregador (es)) 2020. Reutilização permitida de acordo com CC BY-NC. Nenhuma reutilização comercial. © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. Palavras-chave: Criança; Gangliosídeos; Imunoglobulinas Intravenosas; Síndrome de Miller-Fisher/ diagnóstico; Síndrome de Miller-Fisher/ tratamento.
Miller-Fisher综合征是一种急性脱髓鞘性多神经病变,典型表现为眼麻痹、反射减退和共济失调。虽然是吉兰-巴罗综合征的一种罕见的变异,但米勒-费舍尔综合征在临床、实验室和影像学上有一些患者年龄组固有的特点。我们提出了一个三岁的病人,提出了三天的历史步态不平衡和眼运动障碍。神经学检查显示完全眼麻痹、尾轴共济失调及反射减退。脑脊液检查显示白蛋白细胞分离,而神经传导检查,脑磁共振成像和抗神经节苷脂抗体筛查未显示。患者被诊断为Miller-Fisher综合征,并开始静脉注射人免疫球蛋白(2g /kg) 5天。确诊3个月后,患者完全康复,神经学检查无明显异常。认识到儿童米勒-费舍尔综合征的特殊性,克服在年轻患者中进行准确神经学检查的困难,认识到儿童米勒-费舍尔综合征鉴别诊断的多重因素,是正确诊断和制定适当治疗策略的关键。Informações/资料:Caso Clínico, publicado em Sinapse,第20卷,Número 1, janeiro- maro 2020。vers o eletrónica em www.sinapse.pt病例报告,发表于Sinapse,第20卷,第1期,2020年1月至3月。电子版本www.sinapse.pt©Autor (es) (ou seu (s) empreador (es)) 2020。reuseza o permitida de acordo com CC BY-NC。nenhuman reutilization。©作者(或其雇主)2020。在CC BY-NC下允许重复使用。禁止商业再利用。Palavras-chave: Crianca;Gangliosideos;Imunoglobulinas Intravenosas;Síndrome de Miller-Fisher/ diagnóstico;Síndrome de Miller-Fisher/ treatento。
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引用次数: 0
Cefaleia e Doença Celíaca: O Que Há em Comum? 头痛和乳糜泻:有什么共同点?
Q4 Medicine Pub Date : 2020-06-30 DOI: 10.46531/SINAPSE/CC/190027/2020
Ana Carvalho
Celiac disease is a condition with a large spectrum of manifestations that goes far beyond the classic presentation, with poor weight progression. Extra-intestinal manifestations play an important role in the diagnostic approach and should therefore be recognized. Headache may be considered an extra-intestinal manifestation of the disease or may arise throughout its course. There is an increased prevalence of headache in celiac disease patients and vice-versa. We present the case of a 5-year-old boy with a diagnosis of celiac disease (established in the context of investigation for poor weight progression), who had complaints of episodic headache and paroxysmal vertigo. The semiology of the condition, the diagnostic categorization of headache and its accompanying symptoms are discussed, considering its primary or secondary features, in this case to the underlying autoimmune disease. Sinapse | Volume 20 | N.o 1 | January-March 2020 72 Introdução A cefaleia é uma queixa comum em crianças e adolescentes,1 assumindo uma prevalência elevada na população geral e sendo caracterizada por variáveis clínicas muito diversas, de onde resultam vários tipos de diagnósticos (de cefaleias primárias a secundárias, o espectro clínico é muito amplo). Pode apresentar-se como contínua, intermitente ou ocasional e associar-se, por vezes, a náuseas, vómitos ou sintomas neurológicos transitórios. Em crianças, a cefaleia é geralmente benigna, transitória e com um prognóstico favorável, mas o aparecimento dos sintomas supracitados pode fazer com que a expressão clínica de uma entidade dita benigna se transforme num evento com impacto muito negativo no dia-a-dia das crianças e das famílias, desde logo contribuindo para o absentismo escolar e, necessariamente, complicando o relacionamento com os pares.1 A coexistência de diferentes tipos de cefaleia pode dificultar um diagnóstico preciso.2 Ainda assim, é importante concretizá-lo, pois algumas entidades beneficiam de tratamento específico, contribuindo para uma importante redução da frequência das queixas e, naturalmente, para um incremento da qualidade de vida.3 A doença celíaca (DC) é uma enteropatia dependente de glúten,2 sendo considerada uma doença autoimune, desencadeada pela ingestão desse tipo de proteína.4 Tem uma prevalência estimada de aproximadamente 0,7%-2% na população em geral e 0,4%-1,3% em crianças.5,6 Ocorre principalmente no intestino delgado proximal, em indivíduos geneticamente suscetíveis.7 As manifestações clínicas da doença variam e podem incluir desde sintomatologia gastrointestinal típica a queixas intestinais mínimas, incomuns ou ausentes, havendo também possibilidade de ocorrência de manifestações extraintestinais5 Sintomas neurológicos podem constituir-se como manifestação extraintestinal da doença7 (os mais característicos são a ataxia cerebelosa e as queixas sugestivas de uma neuropatia periférica),8 podendo desenvolver-se durante a evolução da mesma ou ser uma apresentação inicial.6 As queixas
腹腔疾病是一种具有广泛表现的疾病,远远超出了经典表现,体重进展缓慢。肠外表现在诊断方法中起着重要作用,因此应予以认识。头痛可能被认为是该疾病的一种肠道外表现,也可能在整个病程中出现。乳糜泻患者头痛的患病率增加,反之亦然。我们报告了一名5岁男孩的病例,他被诊断为乳糜泻(在调查体重进展不佳的背景下确定),并主诉发作性头痛和阵发性眩晕。讨论了这种情况的符号学、头痛的诊断分类及其伴随症状,考虑到其主要或次要特征,在这种情况下是潜在的自身免疫性疾病。引言头痛是儿童和青少年的常见疾病,1假设其在普通人群中的患病率很高,并且具有非常多样化的临床变量,导致各种类型的诊断(从原发性头痛到继发性头痛,临床范围非常广泛)。它可能表现为持续、间歇性或偶尔,有时可能伴有恶心、呕吐或短暂的神经症状。在儿童中,头痛通常是良性的、短暂的,预后良好,但上述症状的出现会导致所谓良性实体的临床表现成为对儿童和家庭日常生活产生非常负面影响的事件,从而导致旷课,使与同龄人的关系复杂化。1不同类型头痛的共存可能会阻碍准确的诊断。2尽管如此,实施它还是很重要的,因为一些实体从特定的治疗中受益,有助于显著降低投诉频率乳糜泻(CD)是一种谷蛋白依赖性肠病,2被认为是一种由摄入这种蛋白质引发的自身免疫性疾病。4据估计,它在普通人群中的患病率约为0.7%-2%,在儿童中约为0.4%-1.3%。5,6它主要发生在近端小肠,遗传易感个体。7该疾病的临床表现各不相同,可能包括典型的胃肠道症状到轻微、异常或无肠道症状,也有可能出现肠外表现5神经系统症状可能构成疾病的肠外表现7(最具特征的是小脑共济失调和提示周围神经病变的主诉),8可能是在其进化过程中发展起来的,也可能是最初的表现。6根据最近发表的一篇综述9,在被诊断为CD的儿童中,头痛的主诉很常见,假设患病率为18.3%(95%CI 10.4%-30.2%),并被描述为具有偏头痛的特征。然而,根据同一作者提出的结果,在75%的头痛儿童中,使用无麸质饮食(对潜在疾病的唯一有效和可用的治疗方法)改善或解决了这种抱怨,4因此可以诊断与稳态障碍相关的头痛(在这种情况下为CD),根据《国际头痛分类》第3版(第2部分,第10章)。10面筋抑制没有改善的儿童可能确实患有原发性头痛(一种偏头痛,鉴于经常报道的临床特征),同时伴有CD,这必然具有其他治疗意义。事实上,两项病例对照研究3,11和两项先前发表的队列研究2,12表明偏头痛和CD之间的联系不是虚假的,事实上,已经确定诊断为偏头痛的个体的CD患病率高于普通人群,(对所有研究的汇总分析确定,CD在已诊断为偏头痛的儿童中的患病率为2.4%[95%CI 1.5%-3.7%])。9因此,仔细的记忆是至关重要的,因为它植根于临床诊断的成功,以及必须实施的治疗策略。我们提出了一个关于这种情况的例子,涉及一名患有CD的儿童和头痛的投诉。
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引用次数: 0
Teleneurology: current situation, opportunities and challenges in Portugal 远程神经病学:葡萄牙的现状、机遇和挑战
Q4 Medicine Pub Date : 2020-06-30 DOI: 10.46531/sinapse/2020/ar/200013/2020
Laura Teixeira
The increasing prevalence and high morbidity and mortality of neurological diseases in Portugal poses new challenges for healthcare Given the unequal regional distribution of neurologists in the country, the implementation of teleneurology emerges as an alternative to improve accessibility to specialised care and to address these long-term challenges In this article, we review the literature regarding the safety, benefits and risks of using teleneurology in different neurological disorders The results show that teleneurology has proven to be a useful tool for patient orientation at primary and hospital level Its potential is particularly relevant in cerebrovascular disorders Teleneurology consultations have been considered satisfactory by patients and healthcare professionals, saving patients and institutions’ time and costs Challenges to its widespread implementation include equipment costs, patient data security and digital (i)literacy
葡萄牙神经系统疾病的患病率和高发病率和死亡率不断上升,对医疗保健提出了新的挑战。鉴于该国神经学家的区域分布不平等,远程神经病学的实施成为改善专业护理可及性和解决这些长期挑战的替代方案。在本文中,我们回顾了有关安全性的文献。在不同的神经系统疾病中使用远程神经病学的益处和风险结果表明,远程神经病学已被证明是一种有用的工具,在初级和医院层面上,它的潜力与脑血管疾病特别相关。远程神经病学会诊已被患者和医疗保健专业人员认为是令人满意的,节省了患者和机构的时间和成本。患者数据安全和数字素养
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引用次数: 0
Mielinólise Pôntica e Extrapôntica Secundária a Hiperglicemia 继发于高血糖的桥脑和桥外骨髓溶解
Q4 Medicine Pub Date : 2020-05-30 DOI: 10.46531/sinapse/in/190038/2020
Manuel Machado
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引用次数: 0
期刊
Sinapse
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