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Central neurocytoma is a very rare brain tumor of young adults (over 100 cases reported worldwide). It is typically found in the lateral ventricles and occasionally in the third ventricle. Symptoms are those of increased intracranial pressure: headache, nausea and vomiting, drowsiness, vision problems and mental changes. Total removal of the tumor is the therapy of choice. Post-operative prognosis is generally good.
Features include always present findings: Hydrocephalus; and very common findings: Intracranial cystic lesion, Abnormal cellular phenotype, and Abnormal lateral ventricle morphology. 19 total HPO annotations.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Brain and nerves | 7 | Hydrocephalus, Depression, Ataxia |
Biomarker and diagnostic research for central neurocytoma has been reported in the published literature.
Phenotype severity distribution: 1 always present feature, 3 very common features, 8 common features.
Estimated prevalence: Unknown (Unknown prevalence).
1 clinical trial registered. Interventions under study include drug therapy. Pipeline includes 1 PHASE4. Research is primarily industry-sponsored.
51 publications have been identified in PubMed for central neurocytoma. Research spans Case Report / Case Series (47%), Clinical Trial Publication (12%), and Basic Science / Preclinical (12%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 24 | 47% |
Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 4:30 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Eyes
2 |
Abnormality of vision, Decreased corneal reflex |
Cellular | 1 | Abnormal cellular phenotype |
Digestive system | 1 | Nausea and vomiting |
Ears | 1 | Tinnitus |
Bones and joints | 1 | Postural instability |
Clinical study results |
6 |
12% |
Laboratory research | 6 | 12% |
Research summaries | 5 | 10% |
Disease patterns and progression | 5 | 10% |
Testing and diagnosis research | 3 | 6% |
Other research | 1 | 2% |
New treatment approaches | 1 | 2% |
Lu TN (2026). [PMID: 42143885](https://pubmed.ncbi.nlm.nih.gov/42143885/). *J Clin Neurosci*. [Review / Meta-Analysis]
Khojah O (2026). [PMID: 41475458](https://pubmed.ncbi.nlm.nih.gov/41475458/). *World Neurosurg*. [Epidemiology / Natural History]
Wee CW (2026). [PMID: 41872623](https://pubmed.ncbi.nlm.nih.gov/41872623/). *J Neurooncol*. [Clinical Trial Publication]
Wang D (2026). [PMID: 41970975](https://pubmed.ncbi.nlm.nih.gov/41970975/). *Front Endocrinol (Lausanne)*. [Case Report / Case Series]
Scravaglieri A (2026). [PMID: 41730194](https://pubmed.ncbi.nlm.nih.gov/41730194/). *J Neurosurg Case Lessons*. [Review / Meta-Analysis]
Bojanowski MW (2026). [PMID: 41421654](https://pubmed.ncbi.nlm.nih.gov/41421654/). *World Neurosurg*. [Case Report / Case Series]
Al-Hussaini M (2026). [PMID: 41992761](https://pubmed.ncbi.nlm.nih.gov/41992761/). *Clin Neuropathol*. [Review / Meta-Analysis]
Jin L (2026). [PMID: 40168511](https://pubmed.ncbi.nlm.nih.gov/40168511/). *Oper Neurosurg*. [Diagnostic / Biomarker]
Kojita Y (2026). [PMID: 41234807](https://pubmed.ncbi.nlm.nih.gov/41234807/). *Radiol Case Rep*. [Case Report / Case Series]
Oshima S (2026). [PMID: 42217076](https://pubmed.ncbi.nlm.nih.gov/42217076/). *Jpn J Radiol*. [Review / Meta-Analysis]