Evidence map›Paper›PMID 33093971›Full record

ArticleSurgical neurology international2020

Hydrocephalus in children - A rare case of pineal cavernoma and literature review.

Ricardo Malcata Nogueira, Luis Santos Cardoso, Lino Fonseca, Miguel Correia, Amets Iraneta, Pedro Roque, Mario Matos, Manuela Mafra

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Surgical neurology international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Hydrocephalus Secondary to Pineal Region Lesions.Advances and technical standards in neurosurgery · 2026
    Review
  2. 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

8 authors at 2 institutions in 1 country.

Ricardo Malcata NogueiraDepartment of Neurosurgery, Centro Hospitalar Universitario Lisboa Central, R. Jose Antonio Serrano, Lisbon, Lisbon, Portugal.
Luis Santos CardosoDepartment of Neurosurgery, Centro Hospitalar Universitario Lisboa Central, R. Jose Antonio Serrano, Lisbon, Lisbon, Portugal.
Lino FonsecaDepartment of Neurosurgery, Centro Hospitalar Universitario Lisboa Central, R. Jose Antonio Serrano, Lisbon, Lisbon, Portugal.
Miguel CorreiaDepartment of Neurosurgery, Centro Hospitalar Universitario Lisboa Central, R. Jose Antonio Serrano, Lisbon, Lisbon, Portugal.
Amets IranetaDepartment of Neurosurgery, Centro Hospitalar Universitario Lisboa Central, R. Jose Antonio Serrano, Lisbon, Lisbon, Portugal.
Pedro RoqueDepartment of Neurosurgery, Centro Hospitalar Universitario Lisboa Central, R. Jose Antonio Serrano, Lisbon, Lisbon, Portugal.
Mario MatosDepartment of Neurosurgery, Centro Hospitalar Universitario Lisboa Central, R. Jose Antonio Serrano, Lisbon, Lisbon, Portugal.
Manuela MafraDepartment of Pathological Anatomy, Centro Hospitalar Universitario Lisboa Central, R. Jose Antonio Serrano, Lisbon, Lisbon, Portugal.
Stony Brook University · USNeurological Surgery · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCavernous malformations prevalence ranges from 0.4 to 0.6% and accounts for 5-15% of all central nervous system vascular malformations. Pineal cavernomas constitute <1% of all locations published in the literature, with a total of 26 cases reported, only 5 regarding the pediatric population until 2020. Overall annual hemorrhage rate is 2.4%. Symptoms are often due to hydrocephalus and intracranial hypertension. CASE DESCRIPTION: We report a case of a 5-year-old child with visual disturbances, headache, and progressive neurologic deterioration. MR showed a lesion in the pineal region and triventricular hydrocephalus. She was submitted to endoscopic third ventriculostomy and total excision of the lesion by the infratentorial supracerebellar approach a few days later. Histopathological examination confirmed a pineal cavernous malformation. The patient returned to her normal life without any neurologic deficit and a normal development.

conclusionThe ideal treatment is primary lesion removal; however, due to the infrequency and because it is a curable lesion, studies seeking to deepen the knowledge of this disease are considered relevant.

Indexed as

Cavernous malformationHydrocephalusPediatricPinealVascular disorders

Identifiers

PMID33093971
PMCPMC7568112
OpenAlexW3094496831

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.