Evidence map›Paper›PMID 26474987›Full record

ArticleEuropean radiology2016

Prenatal MR imaging features of isolated cerebellar haemorrhagic lesions.

Francesca Martino, Mariya Malova, Claudia Cesaretti, Cecilia Parazzini, Chiara Doneda, Luca A Ramenghi, Andrea Rossi, Andrea Righini

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Article in European radiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

6 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Diagnostic Value of Sylvian Fissure Hyperechogenicity in Fetal SAH.AJNR. American journal of neuroradiology · 2022
    Article
  4. Brain fetal neuroradiology: a beginner's guide.Translational pediatrics · 2021
    Review
  5. Review
  6. Review
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.

Francesca MartinoRadiology Department, Ospedale Maggiore della Carità, Corso Mazzini 18, 28100, Novara, Italy.
Mariya MalovaNeonatal Intensive Care Unit, Istituto Giannina Gaslini, Via Gerolamo Gaslini, 5, 16148, Genoa, Italy. mmalova@libero.it.
Claudia CesarettiRadiology and Neuroradiology Department, V. Buzzi Children's Hospital, Via Castelvetro 32, 20154, Milan, Italy.
Cecilia ParazziniRadiology and Neuroradiology Department, V. Buzzi Children's Hospital, Via Castelvetro 32, 20154, Milan, Italy.
Chiara DonedaRadiology and Neuroradiology Department, V. Buzzi Children's Hospital, Via Castelvetro 32, 20154, Milan, Italy.
Luca A RamenghiNeonatal Intensive Care Unit, Istituto Giannina Gaslini, Via Gerolamo Gaslini, 5, 16148, Genoa, Italy.
Andrea RossiNeuroradiology Unit, Istituto Giannina Gaslini, Via Gerolamo Gaslini, 5, 16148, Genoa, Italy.
Andrea RighiniRadiology and Neuroradiology Department, V. Buzzi Children's Hospital, Via Castelvetro 32, 20154, Milan, Italy.
Istituto Giannina Gaslini · ITAzienda Ospedaliero Universitaria Maggiore della Carita · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePrenatal features of isolated cerebellar haemorrhagic lesions have not been sufficiently characterised. We aimed to better define their MR imaging characteristics, documenting the location, extension, evolution stage and anatomic sequelae, and to better understand cerebellar haemorrhage pathophysiology. MATERIALS AND

methodsWe screened our foetal MR imaging database (3200 cases) for reports of haemorrhagic lesions affecting only the cerebellum (without any supratentorial bleeding or other clastic lesions), defined as one of the following: T2-weighted hypointense or mixed hypo-/hyperintense signal; rim of T2-weighted hypointense signal covering the surface of volume-reduced parenchyma; T1-weighted hyperintense signal; increased DWI signal.

resultsSeventeen cases corresponded to the selection criteria. All lesions occurred before the 26th week of gestation, with prevalent origin from the peripheral-caudal portion of the hemispheres and equal frequency of unilateral/bilateral involvement. The caudal vermis appeared affected in 2/3 of cases, not in all cases confirmed postnatally. Lesions evolved towards malformed cerebellar foliation. The aetiology and pathophysiology were unknown, although in a subset of cases intra- and extracranial venous engorgement seemed to play a key role.

conclusionsOnset from the peripheral and caudal portion of the hemispheres seems characteristic of prenatal cerebellar haemorrhagic lesions. Elective involvement of the peripheral germinal matrix is hypothesised. KEY POINTS: • The cerebellum can be vulnerable to bleeding during foetal development. • Isolated cerebellar haemorrhages can be seen on prenatal MRI. • In our cohort, isolated foetal cerebellar haemorrhages occurred before the 26th gestational week. • Haemorrhagic lesions happening in utero could look like malformations on post-natal MRI. • Venous engorgement could have a role in causing cerebellar haemorrhagic lesions.

Indexed as

AdolescentAdultCerebellar DiseasesDiffusion Magnetic Resonance ImagingFemaleFetal DiseasesGestational AgeHumansIntracranial HemorrhagesMagnetic Resonance ImagingMalePregnancyPregnancy Trimester, SecondPrenatal DiagnosisRetrospective StudiesCerebellar cortexCerebellumHaemorrhageMagnetic resonance imagingPrenatal diagnosis

Identifiers

PMID26474987
OpenAlexW2142715971

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Registered trials

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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.