ArticleSurgical neurology international2018
Rapid malignant progression of an intraparenchymal choroid plexus papillomas.
Article in Surgical neurology international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
7 citing papers in PubMed, 9 citations in OpenAlex.
- Choroid plexus carcinoma: state of the field and emerging directions.Oncogenesis · 2026Review
- Giant cystic choroid plexus papilloma mimicking intracerebral hydatid cyst.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026Article
- Choroid Plexus Cyst with Parenchymal Localization in a Symptomatic 50-year-old Male: A Case Report.NMC case report journal · 2026Article
- Article
- Metastatic choroid plexus papilloma presenting as a sellar mass: A case report and literature review.Surgical neurology international · 2024Article
- Choroid Plexus Papilloma of the Fourth Ventricle in a Pediatric Patient: A Case Report.Cureus · 2022Article
- Molecular insights into malignant progression of atypical choroid plexus papilloma.Cold Spring Harbor molecular case studies · 2021Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors at 3 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundChoroid plexus tumors (CPTs) are rare neoplasms accounting for only 0.3-0.6% of all brain tumors in adults and 2-5% in children. The World Health Organization (WHO) classification describes three histological grades: grade I is choroid plexus papilloma (CPP), grade II is atypical papilloma, and grade III is the malignant form of carcinoma. In adults, CPTs rarely have a supratentorial localization. CASE DESCRIPTION: Here we report a very rare case of an intraparenchymal parietal CPP with a rapid histological transition from grade I to grade III WHO in a 67-year-old man, in <7 months.
conclusionBecause of the rarity of these oncotypes, descriptions of each new case are useful, mostly to consider this diagnostic entity in extraventricular brain tumors of adults, despite an unusual location.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.