Clinical Presentation And Management Of Central Neurocytoma In Pediatric Age Group

Authors

  • Arushi Narang
  • Sampada Tambolkar
  • Siddhi Gawhale
  • Devika Chavan
  • Shailaja Mane

DOI:

https://doi.org/10.52783/jns.v14.2977

Keywords:

Central Neurocytoma, Pediatric Brain Tumor, Intraventricular Tumor, Neuro-oncology, Rare Pediatric Tumor

Abstract

Central neurocytoma is a rare, typically benign intraventricular tumor primarily affecting young adults, but its occurrence in the pediatric population is exceptionally uncommon. This case report aims to highlight the clinical presentation, radiologic features, surgical management, and the outcome of a pediatric central neurocytoma. Herewith, we report the case of a toddler who presented with signs of raised intracranial pressure. Magnetic resource imaging (MRI) brain revealed heterogenous soft tissue showing enhancement in right lateral ventricle lesion extending into third ventricle and aqueduct of Sylvius leading to resultant obstructive hydrocephalus.  Patient underwent endoscopic septostomy with maximal safe resection and was diagnosed with Central Neurocytoma (WHO Grade 2) based on immunohistochemistry (IHC) analysis of intraoperative tissue sample. Despite the rarity of central neurocytomas in children, early diagnosis and appropriate management can lead to excellent long-term prognosis, emphasizing the importance of awareness among clinicians of this entity.

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Published

2025-04-03

How to Cite

1.
Narang A, Tambolkar S, Gawhale S, Chavan D, Mane S. Clinical Presentation And Management Of Central Neurocytoma In Pediatric Age Group. J Neonatal Surg [Internet]. 2025Apr.3 [cited 2025Sep.15];14(10S):836-43. Available from: https://www.jneonatalsurg.com/index.php/jns/article/view/2977

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