Cerebellar Liponeurocytoma with High Proliferation Index: Treatment Options

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Cerebellar liponeurocytoma with high proliferation index: treatment options.

First described by Bechtel and collaborators1, cerebellar liponeurocytomas are posterior fossa lesions composed of densely packed neuronal cells admixed with foci of welldifferentiated adipocyte-like cells. Similar tumors have also been referred to as lipomatous medulloblastoma, lipidized medulloblastoma, medullocytoma, neurolipocytoma, lipomatous glioneurocytoma, or lipidized mature neuroectod...

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Recurrent cerebellar liponeurocytoma with supratentorial extension.

Cerebellar liponeurocytoma (LPN) is a rare central nervous system tumour recently recognized as a distinct clinicopathological entity. It was included in the previous 2000 edition of the World Health Organization (WHO) classification as a grade I neoplasm under the heading of glioneuronal tumours1. With increasing recognition of this entity and longer clinical follow-up periods in its investiga...

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Cerebellar liponeurocytoma: case report.

Liponeurocytoma (lipomatous medulloblastoma) is a rarely and recently described tumor. We report an additional case of this uncommon lesion in an adult and we describe its clinical, radiological and histological features. A 45-year-old woman presented with symptoms and signs of increased intracranial pressure and cerebellar dysfunction. Computed tomography (CT) and magnetic resonance imaging (M...

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Cerebellar Liponeurocytoma: Relevant Clinical Cytogenetic Findings

© 2017 The Korean Society of Pathologists/The Korean Society for Cytopathology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/ by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. pISSN 2383-7...

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Cerebellar liponeurocytoma with unusually histopathology: a case report

Cerebellar liponeurocytoma (LPN) is a rare central nervous system tumor. We encountered a 45-year-old woman with cerebellar LPN who had a three months history of headaches and mild ataxia. MRI revealed a mixed signal tumor in the cerebellar vermis. The tumor was totally removed. Histologically, a highly cellular neoplasm composed of monomorphic small round neuronal cells mixed with lipomatous c...

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ژورنال

عنوان ژورنال: Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

سال: 2009

ISSN: 0317-1671,2057-0155

DOI: 10.1017/s0317167100008210