PHACE syndrome: clinical manifestations, diagnostic criteria, and management
An. bras. dermatol
;
93(3): 405-411, May-June 2018. tab, graf
Article
Dans Anglais
| LILACS
| ID: biblio-949868
ABSTRACT
Abstract Infantile hemangioma can be linked to other organ malformations. In 1996, PHACE syndrome was first defined as the association of large and segmental infantile hemangioma, usually on the face, head, or cervical region, with malformations of the posterior fossa of the brain, arterial anomalies of the central nervous system, coarctation of the aorta, cardiac defects, and ocular abnormalities. Over 300 cases of PHACE syndrome have been reported, and it is cconsidered one of the most common neurocutaneous vascular disorders in childhood. Knowledge of the features and locations of lesions that imply a greater risk of systemic involvement is crucial for the diagnosis and proper management of PHACE syndrome patients. This review highlights the diagnostic criteria for PHACE syndrome, the imaging workup for extracutaneous involvement, the treatment of infantile hemangioma, and the importance of a multidisciplinary approach in the management of these patients.
Texte intégral:
Disponible
Indice:
LILAS (Amériques)
Sujet Principal:
Coarctation aortique
/
Tumeurs de la face
/
Malformations oculaires
/
Syndromes neurocutanés
/
Hémangiome
Type d'étude:
Etude diagnostique
/
Etude d'étiologie
Limites du sujet:
Humains
langue:
Anglais
Texte intégral:
An. bras. dermatol
Thème du journal:
Dermatologie
Année:
2018
Type:
Article
Pays d'affiliation:
Brésil
Institution/Pays d'affiliation:
Universidade Federal de Minas Gerais/BR
/
Universidade de São Paulo/BR
Documents relatifs à ce sujet
MEDLINE
...
LILACS
LIS