Evidence map›Paper›PMID 26525217›Full record

ArticleCerebellum (London, England)2016

Cerebellar Bottom-of-Fissure Dysplasia-a Novel Cerebellar Gray Matter Neuroimaging Pattern.

Andrea Poretti, Andrea Capone, Anette Hackenberg, Ingeborg Kraegeloh-Mann, Gerhard Kurlemann, Guido Laube, Joachim Pietz, Mareike Schimmel, Wolfram Schwindt, Ianina Scheer and 1 more

Abstract read
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In one paragraph

Article in Cerebellum (London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 19% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Cerebellar Watershed Injury in Children.AJNR. American journal of neuroradiology · 2020
    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

11 authors at 6 institutions in 3 countries.

Andrea PorettiDivision of Pediatric Neurology, University Children's Hospital, Steinwiesstrasse 75, CH-8032, Zürich, Switzerland.
Andrea CaponeDivision of Pediatric Neurology, Children's Hospital, Aarau, Switzerland.
Anette HackenbergDivision of Pediatric Neurology, University Children's Hospital, Steinwiesstrasse 75, CH-8032, Zürich, Switzerland.
Ingeborg Kraegeloh-MannDivision of Pediatric Neurology and Developmental Medicine, University Children's Hospital, Tübingen, Germany.
Gerhard KurlemannDivision of Pediatric Neurology, University Children's Hospital, Münster, Germany.
Guido LaubeDivision of Pediatric Neurology, University Children's Hospital, Heidelberg, Germany.
Joachim PietzDivision of Pediatric Nephrology, University Children's Hospital, Zürich, Switzerland.
Mareike SchimmelDivision of Pediatric Neurology, Children's Hospital, Augsburg, Germany.
Wolfram SchwindtDivision of Neuroradiology, University Hospital, Münster, Germany.
Ianina ScheerDivision of Diagnostic Imaging, University Children's Hospital, Zürich, Switzerland.
Eugen BoltshauserDivision of Pediatric Neurology, University Children's Hospital, Steinwiesstrasse 75, CH-8032, Zürich, Switzerland. Eugen.Boltshauser@bluewin.ch.
University Children's Hospital Zurich · CHUniversity Hospital Münster · DEHeidelberg University · DEKantonsspital Aarau · CHUniversity Children's Hospital Tübingen · DEUniversity Hospital Augsburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report on seven patients with a novel neuroimaging finding that involves exclusively the cerebellar gray matter at the bottom of several fissures of both hemispheres but spares the vermis. The abnormal fissures were predominantly located in the lower and lateral parts of the cerebellar hemispheres. The affected cerebellar cortex was hypointense on T1-weighted and hyperintense on T2-weighted and fluid attenuation inversion recovery sequences. In some patients, the involved cerebellar gray matter was mildly thickened and the affected fissures slightly widened. In three of seven patients, the neuroimaging findings were unchanged on follow-up studies up to 6 years. The seven patients had various indications for the brain magnetic resonance imaging studies, and none of them had cerebellar dysfunction. Based on the similarity of the neuroimaging pattern with the cerebral "bottom-of-sulcus dysplasia," we coined the term "cerebellar bottom-of-fissure dysplasia" to refer to this novel neuroimaging finding. The neuroimaging characteristic as well as the unchanged findings on follow-up favors a stable "developmental" (malformative) nature. The lack of cerebellar dysfunction in the affected patients suggests that cerebellar bottom-of-fissure dysplasia represents most likely an incidental finding that does not require specific diagnostic investigation but allows a reassuring attitude.

Indexed as

Magnetic Resonance ImagingNeuroimagingAdolescentCerebellumChildFemaleFollow-Up StudiesGray MatterHumansIncidental FindingsInfantMaleRetrospective StudiesBottom-of-sulcus dysplasiaCerebellar fissureCerebellar gray matterCerebellumFocal cortical dysplasiaIncidental finding

Identifiers

PMID26525217
OpenAlexW2159873661

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.