Acidente vascular cerebral isquêmico em adultos jovens: considerações etiológicas

Stroke affects mainly people aged over 65 years, and atherosclerosis predominates as the main etiopathogenic factor in ischemic stroke (IS). On the other hand, cardiac embolism and arterial dissection are the most frequent causes of IS in patients aged less than 45 years. However, inappropriate control of traditional vascular risk factors in young people may be causing a significant increase of atherosclerosis-related IS in this population. Furthermore, a variety of etiologies, many of them uncommon, must be investigated. In endemic regions, neurocysticercosis and Chagas' disease deserve consideration. Undetermined cause has been still reported in as many as one third of young stroke patients

Cerebral microbleeds and intravenous thrombolysis: case report Micro-hemorragias cerebrais e trombólise endovenosa: relato de caso

Intravenous thrombolysis is an important procedure that has significant impact on ischemic stroke prognosis. However, intracranial hemorrhage (ICH) is a feared complication of this procedure. It has been suggested that cerebral microbleeds (CMBs) may increase the risk of ICH after thrombolysis. We report on a 69 years-old woman with multiple CMBs submitted to intravenous thrombolysis without complications.<br>A trombólise endovenosa é um procedimento importante que tem impacto significativo sobre o prognóstico de pacientes com acidente vascular cerebral isquêmico. Contudo, a hemorragia intracraniana (HIC) é complicação temida deste procedimento. Foi sugerido que micro-hemorragias cerebrais (MHC) aumentem o risco de HIC após trombólise. Relatamos o caso de mulher de 69 anos com múltiplas MHCs submetida a trombólise endovenosa sem complicações

Evitando erros no diagnóstico de doença oclusiva da artéria basilar: pistas clínicas e radiológicas - relato de caso

CONTEXT: The aim of this paper was to report on the characteristics that aid in establishing the diagnosis of basilar artery occlusive disease (BAOD) among patients with hemiparesis and few or minor symptoms of vertebrobasilar disease. CASE REPORT: This report describes two cases in a public university hospital in São Paulo, Brazil. We present clinical and imaging findings from two patients with hemiparesis and severe BAOD, but without clinically relevant carotid artery disease (CAD). One patient presented transient ischemic attacks consisting of spells of right hemiparesis that became progressively more frequent, up to twice a week. The neurological examination revealed slight right hemiparesis and right homonymous hemianopsia. Magnetic resonance imaging (MRI) revealed pontine and occipital infarcts. Magnetic resonance angiography and digital subtraction angiography revealed severe basilar artery stenosis. The other patient presented sudden left-side hemiparesis and hypoesthesia. One year earlier, she had reported sudden onset of vertigo that, at that time, was attributed to peripheral vestibulopathy and was not further investigated. MRI showed a right-side pontine infarct and an old infarct in the right cerebellar hemisphere. Basilar artery occlusion was diagnosed. Both patients presented their symptoms while receiving aspirin, and became asymptomatic after treatment with warfarin. CONCLUSIONS: Misdiagnosing asymptomatic CAD as the cause of symptoms in BAOD can have disastrous consequences, such as unnecessary carotid endarterectomy and exposure to this surgical risk while failing to offer the best available treatment for BAOD. Clinical and imaging features provided important clues for diagnosis in the cases presented.CONTEXTO: O objetivo deste artigo foi de relatar as características que auxiliam no estabelecimento do diagnóstico da doença oclusiva da artéria basilar (DOAB) em pacientes com hemiparesia e poucos sintomas, ou sintomas leves de doença vertebrobasilar. RELATO DE CASO: Descrição de dois casos em um hospital público universitário em São Paulo, Brasil. Apresentamos características clínicas e radiológicas de dois pacientes com hemiparesia e DOAB grave, na ausência de doença carotídea (DCA) relevante. Um paciente apresentou ataques isquêmicos transitórios consistindo de hemiparesia direita transitória, que se tornaram progressivamente mais frequentes, até duas vezes por semana. O exame neurológico revelou hemiparesia direita e hemianopsia homônima direita. A ressonância magnética (RM) revelou infartos pontinos e occipitais. As angiografias por ressonância magnética e por subtração digital revelaram estenose grave da artéria basilar. Outra paciente apresentou hemiparesia e hipoestesia de instalação súbita, à esquerda. Um ano antes, ela havia apresentado vertigem súbita, na ocasião atribuída a vestibulopatia periférica, não investigada em maior profundidade. A RM mostrou infarto pontino à direita e infarto antigo no hemisfério cerebelar direito. Foi diagnosticada oclusão da artéria basilar. Ambos os pacientes apresentaram os sintomas enquanto faziam tratamento com aspirina, e se tornaram assintomáticos após tratamento com warfarina. CONCLUSÕES: O diagnóstico errôneo de DCA como causa de sintomas na DOAB pode ter conseqüências desastrosas, como a endarterectomia carotídea desnecessária e a exposição a tal risco cirúrgico, ao invés de oferecimento do melhor tratamento disponível para a DOAB. Características clínicas e radiológicas forneceram pistas importantes para o diagnóstico nos casos apresentados

Avoiding pitfalls in diagnosing basilar artery occlusive disease: clinical and imaging clues - case report

CONTEXT: The aim of this paper was to report on the characteristics that aid in establishing the diagnosis of basilar artery occlusive disease (BAOD) among patients with hemiparesis and few or minor symptoms of vertebrobasilar disease. CASE REPORT: This report describes two cases in a public university hospital in São Paulo, Brazil. We present clinical and imaging findings from two patients with hemiparesis and severe BAOD, but without clinically relevant carotid artery disease (CAD). One patient presented transient ischemic attacks consisting of spells of right hemiparesis that became progressively more frequent, up to twice a week. The neurological examination revealed slight right hemiparesis and right homonymous hemianopsia. Magnetic resonance imaging (MRI) revealed pontine and occipital infarcts. Magnetic resonance angiography and digital subtraction angiography revealed severe basilar artery stenosis. The other patient presented sudden left-side hemiparesis and hypoesthesia. One year earlier, she had reported sudden onset of vertigo that, at that time, was attributed to peripheral vestibulopathy and was not further investigated. MRI showed a right-side pontine infarct and an old infarct in the right cerebellar hemisphere. Basilar artery occlusion was diagnosed. Both patients presented their symptoms while receiving aspirin, and became asymptomatic after treatment with warfarin. CONCLUSIONS: Misdiagnosing asymptomatic CAD as the cause of symptoms in BAOD can have disastrous consequences, such as unnecessary carotid endarterectomy and exposure to this surgical risk while failing to offer the best available treatment for BAOD. Clinical and imaging features provided important clues for diagnosis in the cases presented

Síndrome de Tolosa-Hunt: dificuldades no diagnóstico e padrão de resposta à prednisona Tolosa-Hunt syndrome: troubles in diagnosing and pattern of response to prednisone

A síndrome de Tolosa-Hunt (STH) consiste de oftalmoplegia dolorosa relacionada a processo inílamatório granulomatoso no seio cavernoso. Seu diagnóstico só pode ser firmado quando outras causas potenciais de oftalmoplegia dolorosa forem descartadas. Resposta satisfatória e padronizada a corticosteróides, associada a evolução benigna, pode reforçar essa possibilidade, embora pseudotumor orbitário e neoplasias do tipo linfoma e até meningioma possam suscitar dúvidas no diagnóstico diferencial, pois também podem apresentar boa resposta a essa medicação. Faz-se necessário, portanto, ampla investigação complementar. Apresentamos estudo clínico-radiológico-laboratorial de cinco pacientes com STH. Prednisona foi utilizada em doses entre 40 e 80 mg/dia. Houve resposta analgésica excelente, com remissão da dor em menos de 48 horas em 4 pacientes. Houve melhora mais lenta da oftalmoplegia, que regrediu completamenteentre 4 e 45 dias em todos os pacientes.<br>The Tolosa-Hunt syndrome (THS) consists of a painful ophthalmoplegia related to granulomatous inflammatory process in the cavernous sinus. According to recent concepts, the diagnosis is established only when other causes of painful ophthalmoplegia are ruled out. A typical pattern of response to corticosteroids associated with a benign evolution may reinforce this possibility. Tumors such as lymphoma and meningioma and orbital pseudotumors can make difficult the differential diagnosis because they also may respond to steroids. Thus it is always necessary to make an extensive ancillary investigation. We performed a clinical, laboratory and radiologic study of five patients with THS. Prednisone was used in all, with dosages ranging from 40 to 80 mg/day. In four patients there was a dramatic analgesic effect in less than 48 hours. Improvement of the ophthalmoplegia was not so fast but occurred in all with a complete remission in 4 to 45 days