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hemangioma/seizures
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Intracranial cavernous angioma initially presenting in pregnancy with new-onset seizures.
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A case of an intracranial cavernous angioma, which presented with headaches and seizures in a pregnant patient, is described. Diagnosis was established with magnetic resonance imaging. A computer-assisted literature search uncovered no previously reported case of intracranial cavernous angioma
Management of cerebral cavernous angiomas in children presenting with seizures.
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Until recently intracranial cavernous angiomas were thought to be rare vascular malformations that usually presented in adulthood as an intracerebral hemorrhage, an expanding mass lesion, or with the new onset of seizures. Prior to the advent of computed tomography (CT), and more recently magnetic
Predictors of Epileptic Seizures and Ability to Work in Supratentorial Cavernous Angioma Located Within Eloquent Brain Areas.
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[An infant with multiple cavernous angiomas presenting with frequent epileptic seizures - detection of epileptic focus by magnetoencephalography].
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We report on a six-year-old girl with frequent partial seizures secondary to multiple cavernous angiomas (CAs) since the age of 17 months. MRI showed two CAs in the left parietal and right frontal lobes. Ictal scalp video EEG demonstrated complex partial seizures of left hemispheric origin,
Removal of a temporal lobe cavernous angioma to control epileptic seizures in a patient with tuberous sclerosis complex
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Purpose: A patient with tuberous sclerosis complex (TSC) and a left temporal cavernous angioma (CA) presented with treatment-resistant epilepsy. We evaluated the patient to determine the best treatment option.
Supratentorial cavernous angiomas and epileptic seizures: preoperative course and postoperative outcome.
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OBJECTIVE
Patients operated on for supratentorial cavernous angiomas were studied to define the incidence and the course of seizures in their clinical history. Electroclinical and neuroradiological data were correlated with the location of cavernomas. The impact of lesionectomy on the outcome of
High levels of glycine and serine as a cause of the seizure symptoms of cavernous angiomas?
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Cavernous angiomas are vascular malformations that cause neurodegeneration and symptoms including epileptiform seizures, headache, and motor deficits. Following neurosurgical removal of the angiomas, patients mostly recover well and become seizure-free. This study reports on the levels of certain
Management of patients with cavernous angiomas presenting epileptic seizures.
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BACKGROUND
The aim of this study was to establish a treatment strategy for patients with cavernous angiomas and have seizures.
METHODS
We analyzed retrospectively 31 patients with cavernous angiomas presenting with seizures. Of the 31 patients, 15 (11 men, 4 women) had been treated medically (the
Partial seizures with visual disturbance treated by radiotherapy of cavernous hemangioma.
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A man aged 26 years had been subject to frequent transient episodes of left homonymous hemianopia, initially accompanied by visual hallucinations and left miosis, since the age of 8 years. These partial seizures recurred 3 to 30 times each month in spite of treatment with anticonvulsant medication.
Cavernous angioma presenting as pregnancy-related seizures.
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OBJECTIVE
To determine the reason that one-quarter to one-third of epileptic women experienced an increased number of seizures during pregnancy. The cause of this increase is not always clearly understood and the principle emphasis of the literature is on the pregnancy-associated changes of
[Epileptic seizures as a symptom of arteriovenous angiomas of the brain].
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Thirteen cases of large cerebral angiomas were followed up for a long time. The authors report on epileptic seizures and point out that epilepsy appears in large malformations, whereas small ones are mostly associated with hemorrhage. The authors describe the clinical picture of every case and the
Case report: seizures in a child caused by a large venous angioma.
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Cerebral venous angioma is a congenital anomaly of the medullary vein, the vessel that drains into the transparenchymal venous stem. This lesion is also referred to as a developmental venous anomaly. A few reports in the literature have documented developmental venous anomaly-related epilepsy,
Co-occurrence of a cerebral cavernous malformation and an orbital cavernous hemangioma in a patient with seizures and visual symptoms: Rare crossroads for vascular malformations.
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BACKGROUND
Cerebral cavernous malformations (CCMs) are angiographically occult vascular malformations of the central nervous system. As a result of hemorrhage and mass effect, patients may present with focal neurologic deficits, seizures, and other symptoms necessitating treatment. Once symptomatic,
Supratentorial cavernous angiomas presenting with seizures: surgical outcomes in 60 consecutive patients.
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The aim of this study is to determine surgical outcomes and factors affecting seizure outcomes in patients who harbor supratentorial cavernous angiomas presenting with seizures. Sixty patients were classified into the intractable epilepsy group (n=22) and the sporadic seizure group (n=38) and then
Seizures abolished by excision of a cavernous hemangioma of the scalp and skull.
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A large vascular malformation of the supraorbital and scalp areas was present in an adolescent girl who had seizures and headaches. Removal of the malformation included the outer table of the skull. The patient has had no seizures during a two-year follow-up.
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