Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Rosette-Forming Glioneuronal Tumor in the Pineal Region: A Series of 6 Cases and Literature Review

8 Sept 2021

Abstract excerpt

Resected lesions from the pineal region are rare specimens encountered by surgical pathologists, and their heterogeneity can pose significant diagnostic challenges. Here, we reviewed 221 pineal region lesions resected at New York-Presbyterian Hospital/Columbia University Irving Medical Center from 1994 to 2019 and found the most common entities to be pineal parenchymal tumors (25.3%), glial neoplasms (18.6%), and...

Topics

Join the communities discussing this publication.

Brain Metastases and Treatment
Glioma Diagnosis and Treatment
Vascular Malformations Diagnosis and Treatment

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 34498065
DOI: 10.1093/jnen/nlab089

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Rosette-Forming Glioneuronal Tumor in the Pineal Region: A Series of 6 Cases and Literature ReviewPMID 34498065Read ↗

Clinicopathological analysis of rosette-forming glioneuronal tumors.Semantic proximity Read ↗

Rosette-forming glioneuronal tumor: a pineal region case with IDH1 and IDH2 mutation analyses and literature review of 43 cases.Semantic proximity Read ↗

PIK3CA mutation in a mixed dysembryoplastic neuroepithelial tumor and rosette forming glioneuronal tumor, a case report and literature review.Semantic proximity Read ↗

Clinical, radiological, and pathological features of 16 papillary glioneuronal tumors.Semantic proximity Read ↗

Histopathologic review of pineal parenchymal tumors identifies novel morphologic subtypes and prognostic factors for outcome.Semantic proximity Read ↗

Rosette‑forming glioneuronal tumor in the Posterior Fossa: Case Report and Literature ReviewSemantic proximity Read ↗

Clinical and molecular heterogeneity of pineal parenchymal tumors: a consensus studySemantic proximity Read ↗

Molecular Profiling of a Rare Rosette-Forming Glioneuronal Tumor Arising in the Spinal CordSemantic proximity Read ↗

Comprehensive analysis of diverse low-grade neuroepithelial tumors with FGFR1 alterations reveals a distinct molecular signature of rosette-forming glioneuronal tumor.Semantic proximity Read ↗

Pineal region glioblastomas display features of diffuse midline and non-midline gliomas.Semantic proximity Read ↗

Rosette‐forming glioneuronal tumours are midline, FGFR1‐mutated tumoursSemantic proximity Read ↗

The histomolecular criteria established for adult anaplastic pilocytic astrocytoma are not applicable to the pediatric populationSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.