pinealoma/эпилептический припадок

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Widespread functional deficits in perception-related networks demonstrated by PET in a case with simple visual seizures.

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OBJECTIVE To study benzodiazepine receptor (BZR) density and functional deficits in occipital lobe epilepsy. METHODS A 39-year-old man who had simple partial visual seizures after neurosurgical transtentorial extirpation of a pinealoma was studied by EEG, magnetic resonance imaging (MRI), and

[A case of pineoblastoma successfully treated with surgery, combined chemotherapy of cisplatin and etoposide, and radiotherapy].

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A 5-year-old girl was admitted to another clinic because of vomiting and convulsions. She was brought to our clinic after a ventriculoperitoneal shunt was inserted. CT scan on admission in our clinic showed a tumor in the pineal region with tumoral hemorrhage. Tumor markers such as HCG, AFP, CEA,

Primary pineal tumors: outcome and prognostic factors--a study from the Rare Cancer Network (RCN).

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OBJECTIVE To better define outcome and prognostic factors in primary pineal tumors. METHODS Thirty-five consecutive patients from seven academic centers of the Rare Cancer Network diagnosed between 1988 and 2006 were included. Median age was 36 years. Surgical resection consisted of biopsy in 12

[An autopsy case of pinealoma treated by irradiation about four years ago (author's transl)].

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The patient was a thirty years old male, who was diagnosed as having pineal body tumors in June,1969, and treated by irradiation after a ventriculo-atrial shunt operation. He recovered well, and participated in some simple work. In May 1972, he suddenly had convulsions followed by incontinence, and

Pineal region tumors: Long-term results of endoscopic third ventriculostomy and concurrent tumor biopsy with a single entry approach in a series of 64 cases.

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Endoscopic third ventriculostomy and concurrent biopsy is increasingly used in management of the pineal region tumors. Our objective was to assess the results of single entry approach to surgically manage the tumors of the pineal region.A retrospective

Pediatric pineal tumors: need for a direct surgical approach and complications of the occipital transtentorial approach.

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In an investigation of the benefits and risks of direct surgical approaches to pediatric pineal tumors, the need for such approaches, the feasibility of surgical removal and operative complications were evaluated in 25 histologically proven cases. Five tumors were germinomas (GEs) or GE-predominant

Neuraxis dissemination in pediatric brain tumors. Response to preirradiation chemotherapy.

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Of 29 consecutive children treated for malignant primary tumors of the central nervous system (CNS) at this institution, postoperative examination showed radiographic or cytologic evidence of neuraxis dissemination in 10 (34%). Given the historically poor results in disseminated CNS tumors treated

Epilepsy in patients with pineal gland cyst.

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OBJECTIVE The aim of the study is to describe types of epileptic seizures in patients with pineal gland cyst (PGC) and their outcome during follow up period (6-10 years). We wanted to determine whether patients with epilepsy differ in PGC volume and compression of the PGC on surrounding brain

Neonatal neoplasms.

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OBJECTIVE To describe neoplasms diagnosed in children

[Germ cell and embryonal tumors].

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Germ cell tumors, which constitute approximately 3-5% of tumors of the central nervous system (CNS), can be subdivided into germinomas, embryonal carcinomas, yolk sac tumors, choriocarcinomas, teratomas and mixed germ cell tumors. The diagnosis of intracranial germ cell tumor is based on the

Tumors of the lateral and third ventricle: surgical management and outcome analysis in 42 cases.

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OBJECTIVE To discuss the clinical presentation, pathological diagnosis, and surgical outcome for a series of 42 consecutive patients treated for lateral and third ventricular tumors. METHODS This is a retrospective series study conducted between 2001 and 2015 and included 42 patients (mean age: 25

[Surgical treatment of intraventricular tumors].

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In the last 11 years we operated on 20 patients (1.03% of all operated brain tumors) with lateral ventricular masses. Anamnesis lasted from 6 months in the case of epileptic seizures to 6 years when headache was the main symptom of disease only. Tumor was located in the anterior cornu and pars

Glioblastoma multiforme of the pineal region: case report.

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OBJECTIVE pineal region tumors are uncommon, and comprise more frequently three categories: germ cell, parenchymal cell and glial tumors. Most pineal gliomas are low-grade astrocytomas. Glioblastoma multiforme, the most aggressive and common brain tumor, is extremely rare at this location with only

An analysis of the respective risks of hematoma formation in 361 consecutive morphological and functional stereotactic procedures.

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OBJECTIVE The risk of hematoma formation in stereotactic procedures is generally considered to range between 1 and 4%, and it has been speculated that morphological procedures may have a higher risk of bleeding than functional procedures. METHODS Between 1989 and 1999, all patients who underwent a

Angelman syndrome assessed by neurological and molecular cytogenetic investigations.

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Angelman syndrome (AS) is characterized by severe psychomotor retardation, speech impairment, happy disposition with bursts of laughter, ataxia, convulsions, and some distinct physical anomalies. Correct diagnosis of AS is important because of its clinical implications, and once the disease is

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