Late growth of infantile hemangiomas in children >3 years of age: A retrospective study.


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 06 10 2017
revised: 16 07 2018
accepted: 23 07 2018
pubmed: 9 10 2018
medline: 7 3 2019
entrez: 9 10 2018
Statut: ppublish

Résumé

The proliferative phase of infantile hemangiomas (IHs) is usually complete by 9 months of life. Late growth beyond age 3 years is rarely reported. To describe the demographic and clinic characteristics of a cohort of patients with late growth of IH, defined as growth in a patient >3 years of age. A multicenter, retrospective cohort study. In total, 59 patients, 85% of which were female, met the inclusion criteria. The mean first episode of late growth was 4.3 (range 3-8.5) years. Head and neck location (55/59; 93%) and presence of deep hemangioma (52/59; 88%) were common characteristics. Posterior fossa malformations, hemangiomas, arterial anomalies, cardiac defects, eye abnormalities (PHACE) syndrome was noted in 20 of 38 (53%) children with segmental facial IH. Systemic therapy (corticosteroid or β-blocker) was given during infancy in 58 of 59 (98%) and 24 of 59 (41%) received systemic therapy (β-blockers) for late IH growth. The retrospective nature and ascertainment by investigator recall are limitations of the study. Late IH growth can occur in children after 3 years of age. Risk factors include head and neck location, segmental morphology, and involvement of deep dermal/subcutaneous tissues.

Sections du résumé

BACKGROUND BACKGROUND
The proliferative phase of infantile hemangiomas (IHs) is usually complete by 9 months of life. Late growth beyond age 3 years is rarely reported.
OBJECTIVE OBJECTIVE
To describe the demographic and clinic characteristics of a cohort of patients with late growth of IH, defined as growth in a patient >3 years of age.
METHODS METHODS
A multicenter, retrospective cohort study.
RESULTS RESULTS
In total, 59 patients, 85% of which were female, met the inclusion criteria. The mean first episode of late growth was 4.3 (range 3-8.5) years. Head and neck location (55/59; 93%) and presence of deep hemangioma (52/59; 88%) were common characteristics. Posterior fossa malformations, hemangiomas, arterial anomalies, cardiac defects, eye abnormalities (PHACE) syndrome was noted in 20 of 38 (53%) children with segmental facial IH. Systemic therapy (corticosteroid or β-blocker) was given during infancy in 58 of 59 (98%) and 24 of 59 (41%) received systemic therapy (β-blockers) for late IH growth.
LIMITATIONS CONCLUSIONS
The retrospective nature and ascertainment by investigator recall are limitations of the study.
CONCLUSION CONCLUSIONS
Late IH growth can occur in children after 3 years of age. Risk factors include head and neck location, segmental morphology, and involvement of deep dermal/subcutaneous tissues.

Identifiants

pubmed: 30293898
pii: S0190-9622(18)32368-5
doi: 10.1016/j.jaad.2018.07.061
pii:
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Propranolol 9Y8NXQ24VQ

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

493-499

Commentaires et corrections

Type : CommentIn

Informations de copyright

Crown Copyright © 2018. Published by Elsevier Inc. All rights reserved.

Auteurs

Kathleen F O'Brien (KF)

Georgetown University School of Medicine, Washington DC.

Sonal D Shah (SD)

University of California, San Francisco, California. Electronic address: sonal.shah@ucsf.edu.

Elena Pope (E)

The Hospital for Sick Children, Toronto, Canada; University of Toronto, Toronto, Canada.

Roderic J Phillips (RJ)

Royal Children's Hospital, Melbourne, Australia.

Francine Blei (F)

Lenox Hill Hospital, Northwell Health, New York, New York.

Eulalia Baselga (E)

Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Maria C Garzon (MC)

Department of Dermatology, Columbia University, New York, New York; Department of Pediatrics, Columbia University, New York, New York.

Catherine McCuaig (C)

Sainte-Justine University Hospital Center, Montreal, Canada.

Anita N Haggstrom (AN)

Department of Dermatology, Indiana University, Indianapolis, Indiana; Department of Pediatrics, Indiana University, Indianapolis, Indiana.

Peter H Hoeger (PH)

Department of Pediatric Dermatology, Catholic Children's Hospital Wilhelmstift, Hamburg, Germany.

James R Treat (JR)

Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Marissa J Perman (MJ)

Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Jane S Bellet (JS)

Department of Dermatology and Pediatrics, Duke University, Durham, North Carolina.

Xavier Cubiró (X)

Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Jeffrey Poole (J)

Children's Hospital New Orleans, New Orleans, Louisiana.

Ilona J Frieden (IJ)

University of California, San Francisco, California.

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Classifications MeSH