Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

The Retinoblastoma Gene01:20

The Retinoblastoma Gene

5.0K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
5.0K
The Retinoblastoma Gene01:20

The Retinoblastoma Gene

2.9K
2.9K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Single-Fraction Stereotactic Radiosurgery for Benign Perioptic Meningiomas: A Strategy for Long-Term Tumor Control and Radiation-Induced Optic Neuropathy Avoidance With a 10-Year Follow-up.

Journal of Korean medical science·2026
Same author

Resolution Comparison of a Standoff Gel Pad Versus a Liquid Gel Barrier for Nasal Bone Fracture Sonography: A Standardized Crossover Study.

Diagnostics (Basel, Switzerland)·2026
Same author

The Usefulness of DEPAP Flaps for Reconstructing Perineal Defects Caused by Fournier's Gangrene: A Case Report.

Journal of clinical medicine·2025
Same author

Verrucous Carcinoma of the Lower Lip: A Rare Case Mimicking Benign Lesion.

Journal of clinical medicine·2025
Same author

Fractionated Gamma Knife Radiosurgery as a Primary Treatment for Large Brain Metastases.

Journal of Korean medical science·2025
Same author

Volume Retention of Folded Dermal Graft After Augmentation Rhinoplasty.

The Journal of craniofacial surgery·2025

Related Experiment Video

Updated: Apr 20, 2026

Establishment of Orthotopic Patient-derived Xenograft Models for Brain Tumors using a Stereotaxic Device
07:44

Establishment of Orthotopic Patient-derived Xenograft Models for Brain Tumors using a Stereotaxic Device

Published on: May 2, 2025

1.2K

Rare pediatric central neurocytomas.

Ji Hoon Phi1, Dong Gyu Kim2

  • 1Division of Pediatric Neurosurgery, Seoul National University Children's Hospital, Daehak-ro, Jongno-gu, Seoul, 110-744, Republic of Korea.

Neurosurgery Clinics of North America
|November 30, 2014
PubMed
Summary

Central neurocytoma is a rare pediatric brain tumor. Complete surgical removal offers an excellent prognosis, with radiation reserved for residual or recurrent cases in children.

Keywords:
Central neurocytomaChildrenTreatment

More Related Videos

A Protocol for Rapid Post-mortem Cell Culture of Diffuse Intrinsic Pontine Glioma DIPG
08:46

A Protocol for Rapid Post-mortem Cell Culture of Diffuse Intrinsic Pontine Glioma DIPG

Published on: March 7, 2017

17.7K
Co-culture of Glutamatergic Neurons and Pediatric High-Grade Glioma Cells Into Microfluidic Devices to Assess Electrical Interactions
07:39

Co-culture of Glutamatergic Neurons and Pediatric High-Grade Glioma Cells Into Microfluidic Devices to Assess Electrical Interactions

Published on: November 17, 2021

4.1K

Related Experiment Videos

Last Updated: Apr 20, 2026

Establishment of Orthotopic Patient-derived Xenograft Models for Brain Tumors using a Stereotaxic Device
07:44

Establishment of Orthotopic Patient-derived Xenograft Models for Brain Tumors using a Stereotaxic Device

Published on: May 2, 2025

1.2K
A Protocol for Rapid Post-mortem Cell Culture of Diffuse Intrinsic Pontine Glioma DIPG
08:46

A Protocol for Rapid Post-mortem Cell Culture of Diffuse Intrinsic Pontine Glioma DIPG

Published on: March 7, 2017

17.7K
Co-culture of Glutamatergic Neurons and Pediatric High-Grade Glioma Cells Into Microfluidic Devices to Assess Electrical Interactions
07:39

Co-culture of Glutamatergic Neurons and Pediatric High-Grade Glioma Cells Into Microfluidic Devices to Assess Electrical Interactions

Published on: November 17, 2021

4.1K

Area of Science:

  • Pediatric neuro-oncology
  • Neurosurgery
  • Radiation oncology

Background:

  • Central neurocytoma is an exceptionally rare brain tumor in pediatric populations, accounting for approximately 0.2% of childhood brain tumors.
  • The clinical presentation and management of central neurocytoma in children mirror those in adult patients.

Purpose of the Study:

  • To summarize the current understanding of central neurocytoma in pediatric patients.
  • To highlight the primary treatment modality and prognostic factors.
  • To discuss the role of adjuvant therapies for residual or recurrent disease.

Main Methods:

  • Review of institutional records for pediatric central neurocytoma cases.
  • Analysis of treatment strategies including surgical resection and adjuvant therapies.
  • Evaluation of long-term outcomes and prognostic indicators.

Main Results:

  • Surgical resection is the primary treatment for central neurocytoma.
  • Complete resection is associated with an excellent long-term prognosis in pediatric patients.
  • Adjuvant radiation therapy or radiosurgery may be considered for residual or recurrent tumors, but indications require further clarification.

Conclusions:

  • Central neurocytoma in children, though rare, is managed similarly to adults.
  • Complete surgical resection is crucial for favorable outcomes.
  • Further clinical data accumulation is necessary to refine indications for adjuvant radiation or radiosurgery in pediatric cases.