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dysarthria/hemorrhage
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Dysarthria plus dysphagia is associated with severe sleep-disordered breathing in patients with acute intracerebral hemorrhage.
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OBJECTIVE
Sleep-disordered breathing (SDB) is a risk factor for stroke. The frequency of SDB in Japanese patients with acute intracerebral hemorrhage (ICH) was investigated, as well as factors associated with SDB severity.
METHODS
Between April 2010 and April 2013, patients with ICH within 24 h of
The pulvinar nucleus is associated with the presence of dysarthria in patients with basal ganglia hemorrhage.
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Dysarthria is a frequent symptom in patients with stroke. The anatomical structures responsible for dysarthria have been reported in patients with lacunar infarcts, but the related lesions in patients with basal ganglia hemorrhage (BGH) have not been investigated. The aim of this study was to
Putaminal hemorrhage presenting as dysarthria-clumsy hand syndrome.
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A patient with chronic hypertension presented clinically with the dysarthria--clumsy hand syndrome. A CT scan demonstrated putaminal hemorrhage sparing the internal capsule. This case provides additional evidence that lacunar syndromes may not be due to lacunar infarction. The localization of
Primary pontine hemorrhage and the dysarthria-clumsy hand syndrome.
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Bleeding, dysphagia, dysphonia, dysarthria, severe sore throat, and possible recurrent laryngeal, hypoglossal, and lingual nerve injury associated with routine laryngeal mask airway management: where is the vigilance?
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Dysarthria--clumsy hand syndrome and cerebellar hemorrhage.
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Scanning dysarthria secondary to spontaneous midbrain hemorrhage: case report and review of literature.
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Non-aneurysmal subarachnoid hemorrhage as presentation of moyamoya disease in an adult.
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BACKGROUND
The presentation of moyamoya disease (MMD) as an aneurysmal subarachnoid hemorrhage (SAH) is relatively frequent and in the absence of aneurysms is extremely rare.
METHODS
A 53-year-old male patient suddenly developed severe headache associated with dysarthria and an altered state of
Dural arteriovenous fistula manifesting as pontine hemorrhage at the craniocervical junction.
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Craniocervical junction (CCJ) dural arteriovenous fistula (DAVF) manifesting as intracerebral hemorrhage is extremely rare. We report the first case of CCJ-DAVF manifesting as pontine hemorrhage. A 69-year-old male presented with a pontine hemorrhage manifesting as a sudden onset of right
Intracerebral Hemorrhage after Carotid Artery Stenting without Evidence of Hyperperfusion in Positron Emission Tomography.
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CONCLUSIONS
A 75-year-old man with a recent history of transient left hemiparesis and dysarthria was referred to our hospital. Angiography showed right internal carotid artery (ICA) occlusion and left ICA 89% stenosis. Positron emission tomography (PET) showed decreased cerebral blood flow (CBF),
Primary Central Nervous System Lymphoma Presenting as Growing Intracerebral Hemorrhage.
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BACKGROUND
Hemorrhage at presentation in primary central nervous system (CNS) lymphoma is rare. We encountered a case of primary CNS lymphoma presenting as a growing intracerebral hemorrhage.
METHODS
An 80-year-old man presented with mild dysarthria. Computed tomography demonstrated a round,
Primary Antiphospholipid Antibody Syndrome Complicated with Cerebellar Hemorrhage and Aortic Dissection: A Case Report.
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BACKGROUND Antiphospholipid antibody syndrome (APS) is a systemic autoimmune disease associated with arterial and venous thromboembolism and pregnancy complications. There have been several reports of APS with systemic lupus erythematosus (SLE) complicated with aortic dissection. However, none of
Paradoxical association of moyamoya syndrome with large middle cerebral artery aneurysm and subarachnoid hemorrhage. Case report.
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A 69-year-old woman was admitted to our hospital because of fluctuating dysarthria during the past 2 months. Magnetic resonance imaging revealed old cerebral infarction of the left cerebral hemisphere with acute subarachnoid hemorrhage in the left sylvian fissure. Cerebral angiography showed a large
Mutism and cerebellar dysarthria after brain stem surgery: case report.
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Transient mutism resolving to cerebellar speech after posterior fossa surgery is a well-recognized phenomenon, particularly in pediatric patients. The anatomic basis for this postoperative functional change is unclear but may reside in the dominant superior cerebellar hemisphere or the medial deep
[Follow-up of primary pontine hemorrhage of the young adult by CT scan].
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A case of primary pontine hemorrhage of the young was reported. He was 22 years of age, who did not have the history of hypertension. He suddenly noticed disturbance of skilled act of his right hand and speech disturbance. He was admitted to our clinic two days after the onset. Neurological
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