anaplasia/פרכוס אפילפטי

הקישור נשמר בלוח

מאמריםניסויים קלינייםפטנטים

בחר סוג מיון

עמוד 1 מ 17 תוצאות

Seizure prophylaxis in meningiomas: A systematic review and meta-analysis

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Introduction: No formal indication currently exists for seizure prophylaxis in neurosurgical oncology patients. Neither have specific recommendations been made on the use of antiepileptic drugs (AED) in seizure-free patients with

17-year-old girl with headache and complex partial seizure.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Supratentorial cortical ependymoma is a rare clinical entity where ependymoma occurring in the cortex without any connection to the ventricular system since ependymoma usually arises from the lining of the ventricular system or central canal of spinal cord. There have been 14 such cases reported in

Intracranial and spinal metastases from a ganglioglioma with unusual cytogenetic abnormalities in a patient with complex partial seizures.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

We describe an unusual clinical presentation of a ganglioglioma in a patient with complex partial seizures. The patient underwent a right temporal lobectomy with subtotal tumor resection at age 15 years, followed by a complete resection 1 year later. Follow-up MRI scan a year later documented

Aggressive behavior and anaplasia in pleomorphic xanthoastrocytoma: a plea for a revision of the current WHO classification.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Pleomorphic xanthoastrocytoma (PXA) is a rare astrocytic neoplasm that commonly affects children and young adults, and presents with seizures. PXA is typically supratentorial with a predilection to the temporal lobe, and often involves the cortex and the meninges. PXAs have a favorable prognosis

Gangliogliomas: a clinicopathological study of 25 cases and review of the literature.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

The histopathological, clinical, and radiological findings in 25 patients (median age 20.5 years; range 1.7-64.2 years) with gangliogliomas were assessed to correlate degree of astrocytic anaplasia and proliferative potential with recurrence or survival. Most patients (64%) presented with seizures

Multiple extracranial metastases from secondary glioblastoma: a case report and review of the literature.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Glioblastoma represents extreme anaplasia in astrocytic tumors. In spite of this aggressiveness, extracranial metastasis of glioblastoma is very rare and has been documented in only a few patients in the literature. In this article, a 30-year-old woman with secondary glioblastoma associated with

Rosette-forming glioneuronal tumor: report of an unusual case with intraventricular dissemination.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

A rosette-forming glioneuronal tumor (RGNT) was encountered in a 16-year-old Chinese girl. She experienced seizures with loss of consciousness for 1 month prior to diagnosis. A brain MRI revealed multifocal masses occupying all of the ventricular system associated with marked hydrocephalus. A biopsy

Intraparenchymal meningioma originating from underlying meningioangiomatosis. Case report and review of the literature.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

The authors present the case of a 20-year-old woman with right-sided temporal intraparenchymal meningioma originating from underlying meningioangiomatosis. The patient manifested temporal-type seizures as the initial symptom. She had no stigmata of neurofibromatosis Type 2. Neuroradiological studies

Papillary glioneuronal tumor.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

The descriptive term papillary glioneuronal tumor (PGNT) has been repeatedly applied to a morphologic subset of low-grade mixed glial-neuronal neoplasia of juvenile and young adult patients. We report on a 13-year-old boy with PGNT of the left temporal lobe, who presented with headaches and a single

Oligodendroglioma in childhood.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Fifteen pediatric (age under 16) cases of oligodendroglioma (ODG) were surgically proven from January 1985 to April 1992 at the Division of Pediatric Neurosurgery, Seoul National University Children's Hospital. To observe the proportion of ODG's in primary intracranial tumors, the location of ODG's

Benign isolated fibrohistiocytic tumor arising from the central nervous system. Considerations about two cases.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Benign fibrous histiocytomas (BFHs) are tumors with fibroblastic and histiocytic components without histological anaplasia. Intracerebral lesions are exceptional and to our knowledge a spinal location was not yet described. We describe 2 cases of BFHs of the neural axis: the first, a 22-month-old

[Gliomatosis cerebri: the diagnostic potential of MRT].

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Gliomatosis cerebri is a rare tumor of neuroepithelial origin in middle aged persons presented by deterioration of cognitive functions, psychomotor retardation and cerebral convulsions. MRI predominantly shows a bilateral and diffuse infiltration of midline adjacent brain structures including

Awake surgery for incidental WHO grade II gliomas involving eloquent areas.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

BACKGROUND WHO grade II glioma (G2G) is a pre-malignant tumor, usually revealed by seizures in young patients living normal lives. G2G grows constantly and will inevitably become anaplastic. Surgical resection significantly increases the overall survival by delaying malignant transformation.

Pleomorphic xanthoastrocytoma with anaplastic features: A rare case report and review of literature with reference to current management.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

Pleomorphic xanthoastrocytoma (PXA) is an uncommon tumor constitutes less than 1% of all astrocytic glial neoplasms was first reported in 1979. PXA commonly occurs in young patients and manifests itself first as seizures followed by focal neurological deficits. The role of radiotherapy or

Papillary glioneuronal tumors: A radiopathologic correlation.

רק משתמשים רשומים יכולים לתרגם מאמרים

התחבר הרשם

OBJECTIVE Papillary glioneuronal tumors (PGNT) are a rare and recently recognized tumor entity. The neuroimaging findings were reviewed to determine if any specific findings emerge to assist a preoperative diagnosis of PGNT. METHODS Seven histologically confirmed cases of PGNT were evaluated from

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Herbal & Natural Medicine

המאגר השלם ביותר של צמחי מרפא המגובה על ידי המדע

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