Evidence map›Paper›PMID 40928019›Full record

ArticleActa dermato-venereologica2025

Children Treated for Slow-flow Vascular Malformations: Overall Description and Focus on Complications Such as Cellulitis.

Stephanie Bredy, Emilie Coronas, Caroline Degrugillier-Chopinet, Emeline Cailliau, Benoit Catteau, François Dubos

Abstract read
In one paragraph

Article in Acta dermato-venereologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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

6 authors.

Stephanie BredyCHU Lille, Urgences Pédiatriques & Maladies Infectieuses, Hôpital R. Salengro, Lille, France.
Emilie CoronasCHU Lille, Urgences Pédiatriques & Maladies Infectieuses, Hôpital R. Salengro, Lille, France.
Caroline Degrugillier-ChopinetCHU Lille, Service d'Explorations Fonctionnelles Cardiovasculaires et Cardiologie Infantile, Institut Cœur-Poumon, Lille, France.
Emeline CailliauCHU Lille, Département de Biostatistiques, Lille, France.
Benoit CatteauCHU Lille, Service de Dermatologie Pédiatrique, Institut Cœur-Poumon, Lille, France.
François DubosCHU Lille, Urgences Pédiatriques & Maladies Infectieuses, Hôpital R. Salengro, Lille, France; University of Lille, URL2694: METRICS, Lille, France. francois.dubos@chu-lille.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some patients with slow-flow vascular malformations (SFVMs) develop recurring cellulitis. The main objective of this study was to describe SFVMs in children. Other objectives were to determine the frequency of cellulitis episodes, and the factors associated with the occurrence of cellulitis. This retrospective, longitudinal, single-centre study included all children with SFVMs being managed at Lille University Hospital between 1994 and 2020. Data were collected using a standardized questionnaire. After a descriptive analysis, the variables associated with the onset of cellulitis were analysed; 133 patients (median age at diagnosis: 72 months; 53% girls) were included. SFVMs were: venous (81%), lymphatic-venous (10%), capillary-venous (5%), and lymphatic (4%). Nine children had presented at least 1 episode of cellulitis (7%, 95% CI: 4-12) and 29 episodes were reported (median: 3, interquartile range: 2-4; median age at the first episode: 3.5 years). Cellulitis occurred more frequently in young children, with lymphatic and syndromic forms of SFVM, large SFVMs, affecting skin folds, and without long-term SFVM treatment. In conclusion, the occurrence of cellulitis in patients with a SFVM is rare. However, after the first episode, it frequently becomes recurrent, particularly in some patients with identified risk factors, who may require antibiotic prophylaxis.

Indexed as

CellulitisVascular MalformationsAdolescentAge FactorsChildChild, PreschoolFemaleFranceHumansInfantLongitudinal StudiesMaleRecurrenceRetrospective StudiesRisk FactorsTime Factors

Identifiers

PMID40928019
PMCPMC12427584

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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.