Evidence map›Paper›PMID 24707424›Full record

ArticleCase reports in pediatrics2014

A spinal arteriovenous fistula in a 3-year old boy.

Thomas E M Crijnen, Sandra van Gijlswijk, Jozef De Dooy, Maurits H J Voormolen, Dominique Robert, Philippe G Jorens, Jose Ramet

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Article in Case reports in pediatrics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 94% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 1 institution in 1 country.

Thomas E M CrijnenDepartment of Paediatrics, Antwerp University Hospital (UZA), Wilrijkstraat 10, 2650 Edegem, Belgium.
Sandra van GijlswijkDepartment of Paediatrics, Antwerp University Hospital (UZA), Wilrijkstraat 10, 2650 Edegem, Belgium.ORCID 0000-0002-9146-7655
Jozef De DooyDepartment of Paediatrics, Antwerp University Hospital (UZA), Wilrijkstraat 10, 2650 Edegem, Belgium ; Department of (Paediatric) Intensive Care, Antwerp University Hospital (UZA), Wilrijkstraat 10, 2650 Edegem, Belgium.ORCID 0000-0002-0969-5473
Maurits H J VoormolenDepartment of Radiology, Antwerp University Hospital (UZA), Wilrijkstraat 10, 2650 Edegem, Belgium.
Dominique RobertDepartment of (Paediatric) Intensive Care, Antwerp University Hospital (UZA), Wilrijkstraat 10, 2650 Edegem, Belgium.
Philippe G JorensDepartment of (Paediatric) Intensive Care, Antwerp University Hospital (UZA), Wilrijkstraat 10, 2650 Edegem, Belgium.
Jose RametDepartment of Paediatrics, Antwerp University Hospital (UZA), Wilrijkstraat 10, 2650 Edegem, Belgium.
Antwerp University Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a case of a 3-year-old boy with neurodegeneration. Family history reveals Rendu-Osler-Weber disease. Magnetic resonance imaging (MRI) of the spinal cord and spinal angiography showed a spinal arteriovenous fistula with venous aneurysm, causing compression of the lumbar spinal cord. Embolisation of the fistula was executed, resulting in clinical improvement. A week after discharge he was readmitted with neurologic regression. A second MRI scan revealed an intraspinal epidural haematoma and increase in size of the aneurysm with several new arterial feeders leading to it. Coiling of the aneurysm and fistulas was performed. Postoperative, the spinal oedema increased despite corticoids, causing more extensive paraplegia of the lower limbs and a deterioration of his mental state. A laminectomy was performed and the aneurysm was surgically removed. Subsequently, the boy recovered gradually. A new MRI scan after two months showed less oedema and a split, partly affected spinal chord. This case shows the importance of excluding possible arteriovenous malformations in a child presenting with progressive neurodegeneration. In particular when there is a family history for Rendu-Osler-Weber disease, scans should be performed instantly to rule out this possibility. The case also highlights the possibility of good recovery of paraplegia in paediatric Rendu-Osler-Weber patients.

Identifiers

PMID24707424
PMCPMC3965912
OpenAlexW1976293438

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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.