myxoma/epileptische aanval

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[Cardiac myxoma with central retinal artery occlusion, hemiparesis and epileptic seizure in a 9-year-old patient].

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A cardiac myxoma is a very rare cause for a central retinal artery occlusion (CRAO). We report the case of a nine-year-old boy who had an epileptic seizure, the computer-tomographically suspected diagnosis was intracerebral granulomas of unknown etiology. Five months later he suffered an acute

Convulsions, hemiparesis and central retinal artery occlusion due to left atrial myxoma in child.

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Multiple embolizations were the hallmark of the disease in an 8-year-old boy with a left atrial myxoma. Embolizations occurred initially in both hands and legs, later in the brain with generalized seizures and hemiparesis, and finally in the left eye with occlusion of the central retinal artery and

[Focal seizures in a young man with long term arthromyalgia and recurrent skin lesions. Cardiac myxoma. Neoplastic aneurysm and multiple cerebral infarct due to tumor embolization].

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Odontogenic myxoma in an adolescent with tuberous sclerosis.

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Tuberous sclerosis is a hamartoneoplastic syndrome characterised by early onset of convulsive seizures with mental retardation. Oral abnormalities, including enamel hypoplasia and mucosal fibromas, have been previously reported. We report here a 17-year-old girl with this disorder who had received

Right atrial myxoma in an infant.

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Cardiac myxomas are extremely rare in infancy. We report a case of right atrial myxoma in a 35-day-old male infant (with cyanosis and convulsions). Echocardiography was carried out and a diagnosis of right atrial myxoma was made. Open heart surgery was performed using cardiopulmonary bypass and a

Intracranial metastasis from a glandular variant of atrial myxoma.

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BACKGROUND Intracranial metastases from atrial myxoma producing symptomatic mass lesions are very rare with only ten examples reported in the literature. We report a patient with multiple metastases from a cardiac myxoma which had an unusual histopathology mimicking an adenocarcinoma. METHODS A 35

[Cardiac myxoma metastatic to the brain].

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A case of cardiac myxoma presenting as metastatic brain tumor are reported. The patient was a 44-year-old man. One year prior to this admission, he had suffered stroke, which was characterized by right hemiparesis and dysarthria. The computed tomographic (= CT) scan of the head at that time showed a

Cardiogenic syncope. Seizure versus syncope.

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Our recommendations for the evaluation of the patient with suspected cardiogenic syncope are as follows: An initial thorough history and physical examination of the patient will suggest the diagnosis of cardiogenic syncope in at least 50 per cent of patients. A sudden occurrence of syncope, or "drop

Cardiac myxoma: a diagnostic challenge for the neurologist.

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Three patients with left atrial myxoma presented with prominent neurologic symptoms and signs (cerebrovascular disease and/or syncope) within the past year. Two patients died because antemortem diagnosis was late or missed. One patient was successfully treated. Cardiac myxoma produces protean

A case of left atrial myxoma: anaesthetic management.

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Left Atrial Myxomas are notorious for their varied presentations. We describe one such case which initially presented with hemiparesis and seizures and was diagnosed as cerebral infarction and treated accordingly and decompression craniotomy with hinge flap was done for raised ICP and impending

Endovascular Renal Artery Stent Retriever Embolectomy in a Young Patient With Cardiac Myxoma: Case Report and Review of the Literature.

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OBJECTIVE Cardiac myxomas are common tumors of the heart with disproportionate impact on young patients, occasionally with dramatic systemic dissemination of tumor emboli with catastrophic multiorgan system ischemia. The coincident comorbidities can increase the risk of traditional treatments for

Atrial myxoma: a review of clinical experience at Srinagarind Hospital.

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Thirty-two intracardiac myxoma patients who underwent tumor excision in Srinagarind Hospital between January 1, 1983 and January 30, 1997 were retrospectively reviewed. Clinical presentations, diagnostic method, operative findings, and postoperative course were also analysed. There were 20 female

Left atrial myxoma mimicking mitral stenosis.

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Cardiac myxoma is a benign (non-malignant) neoplasm that represents the most common primary tumour of the heart. We present the case of a 36 year old woman with background hypertension who presented with features of left ventricular failure and seizures, and was found during transthoracic

Malignant astrocytoma six years after the resection of a cerebral metastatic cardiac myxoma: case report.

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We describe a woman who had a total resection of a cardiac myxoma followed 8 months later by a hemorrhage in the right frontal lobe secondary to extravascular metastasis of the myxoma. Six years later, after an asymptomatic follow-up, she developed a recurrence of left-sided seizures and an

Complete detachment of cardiac myxoma causing aortic saddle embolization and cerebral infarction.

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A 30-year-old previously healthy male was brought to our emergency room with loss of consciousness and convulsion. Physical examination showed that the femoral arterial pulses were absent. Two-dimensional transthoracic and transesophageal echocardiography showed no evidence of intracardiac thrombus

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