TY - JOUR
T1 - PHACE without Face? Infantile hemangiomas of the upper body region with minimal or absent facial hemangiomas and associated structural malformations
AU - Nabatian, Adam S.
AU - Milgraum, Sandy S.
AU - Hess, Christopher P.
AU - Mancini, Anthony J.
AU - Krol, Alfons
AU - Frieden, Ilona J.
PY - 2011/5
Y1 - 2011/5
N2 - Infantile hemangiomas can be associated with congenital anomalies such as PHACE syndrome with facial hemangiomas and genitourinary and spinal anomalies in the setting of lower body hemangiomas. We describe five infants in whom segmental hemangiomas involving the upper torso and extremities with absent or small facial hemangiomas were associated with structural anomalies similar to those reported with PHACE syndrome, including three with structural arterial anomalies of the subclavian arteries, three with aortic arch anomalies (right sided or narrowed arch), two with congenital heart disease (atrial septal defect and ventricular septal defect; tetralogy of Fallot), one with a retinal scar, and one with a sternal defect (scar). Two of five had small facial hemangiomas of the lower lip, but none had large segmental hemangiomas of the face. Three of five would have met diagnostic criteria for PHACE but lacked a facial hemangioma of 5 cm in diameter or greater. Patients with segmental arm and thorax hemangiomas may have associated structural abnormalities with overlapping features of PHACE, suggesting that a similar syndrome can occur in this clinical setting.
AB - Infantile hemangiomas can be associated with congenital anomalies such as PHACE syndrome with facial hemangiomas and genitourinary and spinal anomalies in the setting of lower body hemangiomas. We describe five infants in whom segmental hemangiomas involving the upper torso and extremities with absent or small facial hemangiomas were associated with structural anomalies similar to those reported with PHACE syndrome, including three with structural arterial anomalies of the subclavian arteries, three with aortic arch anomalies (right sided or narrowed arch), two with congenital heart disease (atrial septal defect and ventricular septal defect; tetralogy of Fallot), one with a retinal scar, and one with a sternal defect (scar). Two of five had small facial hemangiomas of the lower lip, but none had large segmental hemangiomas of the face. Three of five would have met diagnostic criteria for PHACE but lacked a facial hemangioma of 5 cm in diameter or greater. Patients with segmental arm and thorax hemangiomas may have associated structural abnormalities with overlapping features of PHACE, suggesting that a similar syndrome can occur in this clinical setting.
UR - http://www.scopus.com/inward/record.url?scp=79958038171&partnerID=8YFLogxK
U2 - 10.1111/j.1525-1470.2011.01407.x
DO - 10.1111/j.1525-1470.2011.01407.x
M3 - Article
C2 - 21453307
AN - SCOPUS:79958038171
SN - 0736-8046
VL - 28
SP - 235
EP - 241
JO - Pediatric Dermatology
JF - Pediatric Dermatology
IS - 3
ER -