Evidence map›Paper›PMID 18371183›Full record

ArticleBrain pathology (Zurich, Switzerland)2008

Pineocytoma and pineal parenchymal tumors of intermediate differentiation presenting cytologic pleomorphism: a multicenter study.

Michelle Fèvre-Montange, Alexandru Szathmari, Jacques Champier, Karima Mokhtari, Fabrice Chrétien, Alix Coulon, Dominique Figarella-Branger, Marc Polivka, Pascale Varlet, Emmanuelle Uro-Coste and 2 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Pineal Tumors and Pineal Region Tumors.Advances and technical standards in neurosurgery · 2026
    Review
  3. Histopathology and Molecular Pathology of Pineal Region Tumors.Advances and technical standards in neurosurgery · 2026
    Review
  4. Pineal Gland Parenchyma Tumors.Advances and technical standards in neurosurgery · 2026
    Review
  5. Review
  6. Review
  7. Article
  8. Histopathology and molecular pathology of pediatric pineal parenchymal tumors.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2023
    Review
  9. Article
  10. Binucleated and Multinucleated Neurons are Formed by Fusion.Bulletin of experimental biology and medicine · 2021
    Article
  11. Pineal region tumors: pathophysiological mechanisms of presenting symptoms.American journal of translational research · 2021
    Review
  12. Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 1 institution in 1 country.

Michelle Fèvre-MontangeINSERM, U842, Lyon; Université de Lyon, Lyon 1, Faculté de Médecine Laennec, UMRS842, Lyon, France. montange@lyon.inserm.fr
Alexandru Szathmari
Jacques Champier
Karima Mokhtari
Fabrice Chrétien
Alix Coulon
Dominique Figarella-Branger
Marc Polivka
Pascale Varlet
Emmanuelle Uro-Coste
François Fauchon
Anne Jouvet
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytologic pleomorphism has been described in a limited number of benign pineal tumors, namely pineocytoma (PC) and pineal parenchymal tumors (PPTs) of intermediate differentiation (PPTID). We examined the clinicopathologic features in a retrospective series of 14 cases (seven females and seven males aged from 10 to 65 years) of pleomorphic PPT. Seven cases were PC, with no mitoses and with areas of tumoral cells forming large pineocytomatous rosettes and other areas with giant cells containing hyperchromatic nuclei. The other seven were PPTID, presenting few mitoses (< or =2), a Ki67 proliferation index between 3% and 7%, and predominantly composed of small neoplastic cells and scattered giant cells, sometimes multinucleated. In the 14 tumors, the proportion of pleomorphic areas was variable. Most tumoral cells showed extensive neuronal differentiation with strong expression of neuron-specific enolase, synaptophysin and neurofilaments. Some of the neoplastic cells expressed S100 protein. The follow-up period ranged from 1.2 to 13 years and only one PC and one PPTID progressed after stereotactic biopsy or incomplete resection. The lack of invasiveness and the low proliferation index of these tumors suggest a benign clinical course despite the marked pleomorphism, the latter of which can lead to upgrading.

Indexed as

AdultAgedBrain NeoplasmsChildFemaleHumansImmunohistochemistryMaleMiddle AgedPineal GlandPinealoma

Identifiers

PMID18371183
PMCPMC8095592
OpenAlexW2153949481

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.