Evidence map›Paper›PMID 24641194›Full record

ArticleThe British journal of dermatology2014

Prospective study of infantile haemangiomas: incidence, clinical characteristics and association with placental anomalies.

A Munden, R Butschek, W L Tom, J S Marshall, D M Poeltler, S E Krohne, A B Alió, M Ritter, D F Friedlander, V Catanzarite and 4 more

Open access · greenAbstract read
In one paragraph

Article in The British journal of dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed, 2 pooled it
16.7field-weighted citation impact, top 1% 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

122 citing papers in PubMed, 2 syntheses or guidelines pooled it, 310 citations in OpenAlex.

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  16. PHACE syndrome: looking backward and forward.Orphanet journal of rare diseases · 2025
    Review
  17. Article
  18. Review
  19. Review
  20. Nanotechnology in Infantile Hemangioma Management.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2025
    Article

62 more citing papers are in PubMed but not listed here.

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

14 authors at 6 institutions in 1 country.

A MundenUniversity of California, San Diego School of Medicine, San Diego, CA, U.S.A.
R Butschek
W L Tom
J S Marshall
D M Poeltler
S E Krohne
A B Alió
M Ritter
D F Friedlander
V Catanzarite
A Mendoza
L Smith
M Friedlander
S F Friedlander
Scripps Research Institute · USSharp Mary Birch Hospital for Women & Newborns · USRady Children's Hospital-San Diego · USUniversity of California, San Diego · USHarvard University · USTouro University California · US

Funding

INTEGRINS AND OCULAR ANGIOGENESISR01EY011254 · NEI · SCRIPPS RESEARCH INSTITUTE, THE · PI FRIEDLANDER, MARTIN · 1996 to 2016
$11.5M
Genetic Influence in Pediatric PsoriasisK23AR060274 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TOM, WYNNIS L · 2011 to 2015
$663k
NEI NIH HHS EY11254NEI NIH HHS R01 EY011254NIAMS NIH HHS K23 AR060274NIAMS NIH HHS K23AR060274
6 · The paper itself

Abstract

backgroundThe aetiology and exact incidence of infantile haemangiomas (IHs) are unknown. Prior studies have noted immunohistochemical and biological characteristics shared by IHs and placental tissue.

objectivesWe investigated the possible association between placental anomalies and the development of IHs, as well as the demographic characteristics and other risk factors for IHs. PATIENTS AND

methodsPregnant women (n = 578) were prospectively enrolled and their offspring followed for 9 months. Placental evaluations were performed and demographic data collected on all mother-infant pairs.

resultsWe evaluated 594 infants: 34 haemangiomas [either IH or congenital (CH)] were identified in 29 infants, yielding an incidence of 4·5% for IH (27 infants) and 0·3% for CH (two infants). Placental anomalies were noted in almost 35% of haemangioma-related pregnancies, approximately twice the incidence noted in pregnancies with unaffected infants (P = 0·025). Other risk factors for IH included prematurity (P = 0·016) and low birth weight (P = 0·028). All IHs were present by 3 months of age, and cessation of growth had occurred in all by 9 months of age. Most occurred on the trunk. Of note, 20% of identified IHs were abortive or telangiectatic in nature, small focal lesions that did not proliferate beyond 3 months of age. Only one IH required intervention.

conclusionsThis is the first prospective American study to document the incidence of IHs in infants followed from birth to early infancy. The association with placental anomalies was statistically significant. The overall incidence mirrors prior estimates, but the need for treatment was lower than previously reported.

Indexed as

Placenta DiseasesAdolescentAdultCaliforniaFemaleHemangiomaHumansIncidenceInfantMaleMaternal AgeMiddle AgedPregnancyProspective StudiesRisk FactorsYoung Adult

Identifiers

PMID24641194
PMCPMC4410180
OpenAlexW2045479471

What OpenQuestion holds

Textmetadata
LicenceTDM
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.