Central Neurocytoma

Common Name(s)

Central Neurocytoma

A central neurocytoma (CNC) is a rare brain tumor usually found in people between the ages of 20-40 years old. The tumors are most often benign (non-cancerous). Typical symptoms of this condition may include headaches, increased pressure in the skull, blurred vision, nausea, vomiting, drowsiness and seizures.

Generally, CNC tumors can be completely removed by surgery, but depending on certain qualities of the tumor, such as size and rate of tumor growth, removal of the tumor may need to be followed with radiation therapy. Chemotherapy may be suggested if the tumor returns (recurs). The majority of patients with CNC are cured by the removal of the tumor and become long-term survivors (living tumor free for over 10 years). However, as with any other type of tumor, there is a chance for recurrence or the CNC returning. If you or a member of your family has been diagnosed with a central neurocytoma, talk to your doctor about the most current treatment options. Support groups are also a good source of support and information.

Source: Advocacy organizations associated with the condition.

 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Central Neurocytoma" for support, advocacy or research.

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Central Neurocytoma" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Central Neurocytoma" returned 34 free, full-text research articles on human participants. First 3 results:

MR Spectroscopy to Distinguish between Supratentorial Intraventricular Subependymoma and Central Neurocytoma.
 

Author(s): Fumiaki Ueda, Hiroyuki Aburano, Yasuji Ryu, Yuichi Yoshie, Mitsutoshi Nakada, Yutaka Hayashi, Osamu Matsui, Toshifumi Gabata

Journal: Magn Reson Med Sci. 2017 Jul;16(3):223-230.

 

The purpose of this study was to discriminate supratentorial intraventricular subependymoma (SIS) from central neurocytoma (CNC) using magnetic resonance spectroscopy (MRS).

Last Updated: 31 Dec 1969

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Clinical characteristics and prognostic factors of brain central neurocytoma.
 

Author(s): Yaqi Song, Xinle Kang, Gang Cao, Yongqiang Li, Xilei Zhou, Yusuo Tong, Wanwei Wang

Journal: Oncotarget. 2016 Nov;7(46):76291-76297.

 

This study is designed for the clinical characteristics and prognostic factors of central neurocytoma (CN).

Last Updated: 31 Dec 1969

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Role of adjuvant radiation in the management of central neurocytoma: Experience from a tertiary cancer care center of India.
 

Author(s): S Mallick, S Roy, S Das, N P Joshi, V Roshan, A K Gandhi, M Jana, P K Julka, G K Rath

Journal: Indian J Cancer. ;52(4):590-7.

 

Neurocytoma (NC) is a rare benign neuronal tumor. A complete excision remains curative for most of these tumors, but atypical histology and extra-ventricular location often necessitates adjuvant therapy. We intended to explore the clinico-pathological features and treatment outcome ...

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Central Neurocytoma" returned 3 free, full-text review articles on human participants. First 3 results:

[Treatment of central neurocytoma. Experience at a single institution].
 

Author(s): A Rodríguez De Lope, A De La Lama, N López-Ariztegui, R Martínez, C Conde, C Fiaño, F Vázquez

Journal: Neurocirugia (Astur). 2004 Apr;15(2):128-36; discussion 136-7.

 

Central neurocytomas are classically considered as a rare, intraventricular benign tumours with neuronal differentiation derived from precursor cells of subventricular matrix. However some patients with neoplasms with histologic atypia and elevated proliferation potential may have ...

Last Updated: 31 Dec 1969

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Central neurocytoma--case report.
 

Author(s): T Tamiya, T Furuta, S Asari, A Nishimoto

Journal: Neurol. Med. Chir. (Tokyo). 1990 Mar;30(3):178-83.

 

The authors present a case of central neurocytoma in a 34-year-old female who had experienced intermittent headaches over a 10-year period. On computed tomographic (CT) scans and magnetic resonance images, the tumor appeared as a large, calcified mass occupying both lateral ventricles. ...

Last Updated: 31 Dec 1969

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[Central neurocytoma. Case report].
 

Author(s): M Miyata, H Yamashita, S Shirakata, Z Takeda

Journal: Neurol. Med. Chir. (Tokyo). 1989 Dec;29(12):1148-52.

 

A 24-year-old female was hospitalized for progressive headache and nausea. Computed tomography showed a mass lesion in the left lateral ventricle near the foramen of Monro. On light microscopy, this tumor morphologically resembled an oligodendroglioma. However, ultrastructural examination ...

Last Updated: 31 Dec 1969

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Phase II Pediatric Study With Dabrafenib in Combination With Trametinib in Patients With HGG and LGG
 

Status: Recruiting

Condition Summary: Diffuse Astrocytoma; Anaplastic Astrocytoma; Astrocytoma; Oligodendroglioma, Childhood; Anaplastic Oligodendroglioma; Glioblastoma; Pilocytic Astrocytoma; Giant Cell Astrocytoma; Pleomorphic Xanthoastrocytoma; Anaplastic Pleomorphic Xanthoastrocytoma; Angiocentric Glioma; Chordoid Glioma of Third Ventricle; Gangliocytoma; Ganglioglioma; Anaplastic Ganglioglioma; Dysplastic Gangliocytoma of Cerebrellum; Desmoplastic Infantile Astrocytoma and Ganglioglioma; Papillary Glioneuronal Tumor; Rosette-forming Glioneurona Tumor; Central Neurocytoma; Extraventricular Neurocytoma; Cerebellar Iponeurocytoma

 

Last Updated: 24 May 2018

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