PHACE syndrome: clinical manifestations, diagnostic criteria, and management

• Autor(a) principal: Rotter,Anita
• Data de Publicação: 2018
• Outros Autores: Samorano,Luciana Paula, Rivitti-Machado,Maria Cecília, Oliveira,Zilda Najjar Prado, Gontijo,Bernardo
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Anais brasileiros de dermatologia (Online)
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962018000300405
• topic: Aortic coarctation; Hemangioma; Magnetic resonance imaging; Neurocutaneous syndromes; Propranolol; Stroke

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.