Evidence map›Paper›PMID 39963605›Full record

ArticleFrontiers in cardiovascular medicine2025

Case Report: Two-month-old infant with PHACE syndrome: facial hemangioma and severe complex coarctation of the aorta.

Sánchez-Ortiz David, Deiros-Bronte Lucía, De la Hoz-Marañón Lucía, Feito-Rodríguez Marta, Rey-Lois Juvenal, Salas-Mera Diana, Labrandero-De Lera Carlos, López-Gutiérrez Juan Carlos, Gutiérrez-Larraya Federico

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Article in Frontiers in cardiovascular medicine, 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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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Sánchez-Ortiz DavidCardiology Department, Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
Deiros-Bronte LucíaPediatric Cardiology Department, Hospital Infantil La Paz, Madrid, Spain.
De la Hoz-Marañón LucíaCardiology Department, Hospital General Universitario Doctor Balmis, Alicante, Spain.
Feito-Rodríguez MartaDermatology Department, Hospital Infantil La Paz, Madrid, Spain.
Rey-Lois JuvenalCardiac Surgery Department, Hospital Infantil La Paz, Madrid, Spain.
Salas-Mera DianaPediatric Cardiology Department, Hospital Infantil La Paz, Madrid, Spain.
Labrandero-De Lera CarlosPediatric Cardiology Department, Hospital Infantil La Paz, Madrid, Spain.
López-Gutiérrez Juan CarlosGeneral Surgery Department, Hospital Infantil La Paz, Madrid, Spain.
Gutiérrez-Larraya FedericoPediatric Cardiology Department, Hospital Infantil La Paz, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: PHACE syndrome is an uncommon disorder, marked by large segmental hemangiomas on the face and various developmental anomalies. Significant advancements have been made in its diagnosis, imaging, and understanding of complications since 1996. Case Summary: We describe the first diagnosis case of PHACE syndrome in a one-month and 19-day-old infant who presented with a large facial hemangioma and coarctation of the aorta originating from the left common carotid artery, along with an aberrant course of the right subclavian artery. The complementary diagnostic studies, their surgical correction, and their progression are described. Discussion: Given the rarity of the syndrome (the PHACE Syndrome International Clinical Registry and Genetic Repository has over 270 enrolled individuals) and the importance of early diagnosis of some anomalies it comprises, particularly cardiovascular anomalies, dissemination is considered crucial for general and pediatric cardiologists.

Indexed as

aortic coarctationaortic malformationshemangiomaneural crest migrationPHACE syndrome

Identifiers

PMID39963605
PMCPMC11831542

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