neurocytoma/seizures

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Mesial temporal extraventricular neurocytoma: a rare cause of refractory complex partial seizure.

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OBJECTIVE Mesial temporal extraventricular neurocytoma (mtEVN) is a rare cause of refractory complex focal seizures. The characteristics of this clinical entity are discussed in this article. METHODS We report two cases of mtEVN and review the related literature, with particular emphasis on

Extraventricular neurocytoma with ganglionic differentiation associated with complex partial seizures.

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We report an unusual case of extraventricular ("cerebral") neurocytoma with ganglion cells located in the right temporal lobe in a 9-year-old girl with complex partial seizures and precocious puberty. CT showed a calcified mass with central cystic zones. MR imaging showed a markedly hyperintense

Cerebral neurocytoma: an unusual cause of refractory epilepsy. Case report and review of the literature.

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We report a patient with medically refractory complex partial seizures (CPS) caused by a cerebral neurocytoma located near the amygdala. Neurocytoma represents an important addition to the differential diagnosis and, in particular, must be differentiated from oligodendroglioma and dysembryoplastic

Extraventricular neurocytoma--report of a case.

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Neurocytomas are typically located within the supratentorial ventricular system. Extraventricular neurocytoma is a rare brain tumour that poses diagnostic difficulty. We report a case of cerebral extraventricular neurocytoma. A 44-year-old man presented with a 6-month history of tonic-clonic

[Neurocytoma in the left frontal lobe].

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We report a case of a 7-year-old right-handed girl with neurocytoma in the left frontal lobe. She developed convulsive seizures on the right side of her face at the age of 1 year and 8 months, and CT scan revealed a low density lesion in the left frontal lobe near the Sylvian fissure. CT scan at the

Central Versus Extraventricular Neurocytoma in Children: A Clinicopathologic Comparison and Review of the Literature.

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Central neurocytomas (CN) are rare pediatric CNS tumors most often with a benign clinical course. Occasionally, these tumors occur outside the ventricles and are called extraventricular neurocytomas (EVN). We present a retrospective institutional analysis of children with neurocytoma with prolonged

Cerebral neurocytoma. A new subset of benign neuronal tumors of the cerebrum.

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Three cases of patients with unusual neuronal tumors in the cerebral hemisphere are reported. All were associated with long-standing epileptic seizures. Computed tomography disclosed low-density lesions without contrast enhancement, which were interpreted as either arachnoid cysts or a cerebral

Interhemispheric transcallosal approach for resection of intraventricular central neurocytoma.

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The interhemispheric transcallosal approach is a versatile approach to access intraventricular tumors of the lateral and third ventricles. The advantages of using a transcallosal approach over a classical transcortical approach include a direct midline orientation with symmetrical access to both

Progeny in an inhospitable milieu - solitary intraventricular metastasis from a triple negative breast cancer mimicking central neurocytoma: case report and review of diagnostic pitfalls and management strategies.

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Triple-negative breast cancer (TNBC) is one of the most invasive subtypes of breast cancer with high rates of visceral metastases and recurrence. Choroid plexus metastasis from breast cancer is infrequent despite a high incidence of brain parenchymal

Treatment strategies for huge central neurocytomas.

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Central neurocytomas (CNs), initially asymptomatic, sometimes become huge before detection. We described and analyzed the clinical, radiological, operational and outcome data of 13 cases of huge intraventricular CNs, and discussed the treatment strategies in this study. All huge CNs (n=13) in our

Skull base neurocytoma: case report and review of the literature of extraventricular neurocytomas.

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We report a rare skull base neurocytoma. A 44-year-old female with a history of focal seizure and progressive right-sided weakness sought treatment at an outside institution, where she underwent total resection of a "left medial sphenoid wing paraganglioma" in 1984. In 1995 after experiencing

Mesial temporal extraventricular neurocytoma (mtEVN): A case report and literature review.

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We describe a case of mesial temporal extraventricular neurocytoma (mtEVN) in a 23-year-old male presenting with drug-resistant seizures and review the literature on this rare tumor.A PubMed search was queried using the MeSH term "neurocytoma" and

Interventricular neurocytoma: radiologic features and review of the literature.

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Intraventricular neurocytoma (IN), a recently recognized, benign cerebral tumor of young adults, can be confused with oligodendroglioma and other neoplasms. The authors compared the radiologic features of six pathologically confirmed cases of IN with those of 26 previously reported cases. The

Extraventricular neurocytoma: morphological and immunohistochemical considerations on differential diagnosis.

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Neurocytoma is an unusual neuronal tumor especially affecting young people. It commonly arises in the ventricles and has a benign outcome. Herein, we report on a rare case of extraventricular neurocytomas (right parietal lobe) in a young girl admitted to hospital for a cranial trauma subsequent to a

Clinicopathologic features of intracranial central neurocytomas in 2 dogs.

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BACKGROUND In humans, central neurocytomas are rare and typically benign intracranial tumors found within the lateral ventricles, although extraventricular variants have been reported. Intracranial central neurocytomas have not been previously recognized in domestic animals. OBJECTIVE To describe

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