dysarthria/hoofdpijn

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Legionella pneumophila infection presenting as headache, confusion and dysarthria in a human immunodeficiency virus-1 (HIV-1) positive patient: case report.

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BACKGROUND Legionella pneumophila is a common cause of community-acquired pneumonia. Central nervous system dysfunction is common, and diagnosis in the absence of pulmonary symptoms can be challenging. Here we describe an atypical clinical presentation of Legionella infection in a patient with HIV

Severe headache, dysarthria and ataxia in a 62-year-old man.

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[A 61-year-old male with headache, coffee-ground vomit, disorientation and dysarthria].

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[Language disorders in acute cerebellitis: beyond dysarthria].

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BACKGROUND Acute cerebellitis is one of the main causes of cerebellar syndrome in infancy. Among the wide range of manifestations, headache and ataxia being the most predominant, we can find other less frequent, although nonetheless interesting, ones, such as language disorders, which go beyond the

A case of cluster headache accompanied by myoclonus and hemiparesis.

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BACKGROUND Cluster headache is a primary headache disorder characterized by periodic episodes of intense headache accompanied by autonomic symptoms. We report an unusual clinical presentation of cluster headache that was preceded by myoclonus and accompanied by hemiparesis. METHODS A 26-year-old man

Clinical implications of headache in lacunar stroke: relevance of site of infarct.

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OBJECTIVE To assess whether the infarction topography influenced upon the incidence of headache and the likelihood of neurological recovery in lacunar infarction. BACKGROUND The relationship between topography of infarction and the incidence of headache as well as the influence of headache on

Transient stabbing headache from an acute thalamic hemorrhage.

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Stabbing headache can be encountered in both primary and secondary forms, but has been infrequently reported among patients with stroke, and is not known to be associated with a small well-circumscribed brain lesion. A 95-year-old woman taking warfarin presented with the sudden onset of stabbing

Dysarthria associated with giant cell arteritis.

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Over a one month period, a 74-year-old man developed typical features of giant cell arteritis (GCA) including visual changes, headache, scalp tenderness, and an elevated erythrocyte sedimentation rate. In addition, he had reproducible painless dysarthria that was precipitated by chewing or prolonged

Left internal carotid artery dissection presenting with headache, Collet-Sicard syndrome and sustained hypertension.

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The baroreflex maintains blood pressure through the glossopharyngeal (IX) cranial nerve. We report a 54-year-old man who developed a left sided headache, hoarseness, dysarthria, dysphagia, and sustained hypertension from a left internal carotid artery dissection. We hypothesise that interruption of

De-novo headache with transient vertebro-basilar symptoms: role of embryonic hypoglossal artery.

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We report the case of a 56-year-old man with acute onset of de-novo stabbing, pulsating and diffuse headache with subsequent appearance (within few minutes) of posterior fossa symptoms (vomiting, postural instability, anisocoria, incoordination, dysarthria, retropulsion) lasting 9-12 h. Recurrent

[Vasculitis as a reason of chronic headache].

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A 13-year-old girl presented to our emergency with a one week history of fever and skin rash and new onset of chorea for the last three days. There was a long standing history of right predominant headache; followed by personality change, fatigue, arthralgia and weight loss over the last few months.

Recurrent headaches: a case of neurological Behçet's disease.

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A 48-year-old black male, of Nigerian heritage, presented with a 24-hour history of frontal headache of gradual onset. The headache characteristic was migranous, being described as throbbing in nature and located to the right frontal area with associated blurring of vision. Although similar to prior

[Moyamoya disease: clinical, neuroradiological, neuropsychological and genetic perspective].

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BACKGROUND Moyamoya disease (MMD) is an occlusive cerebrovascular disease characterized by progressive stenosis or occlusion in the terminal portion of the bilateral internal carotid arteries, affecting both children and adults. OBJECTIVE To conduct a review and update on MMD from a clinical,

Neurological complications after liver transplantation.

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This was a single-centre, prospective study to assess the frequency of neurological complications and their impact on prolonged hospitalization in 137 liver transplant patients presenting between September 1997 and June 2010. Neurological complications were seen in 22 (16%) patients during their

[State of lucid delirium after orthotopic liver transplantation. Clinical case].

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Neuropsychiatric complications after liver transplantation are common and have an incidence ranging from 0.5% to 47% in several international reports. They are due to different causes (coagulation, haemodynamic or electrolyte disorders, infections, immunosuppressive drugs). In patients receiving

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