To report a case of PHACE syndrome diagnosed in an infant with large segmental facial hemangiomas and associated congenital anomalies.
Key Findings:
The infant presented with large facial hemangiomas and multiple congenital anomalies including brain malformations and cardiac defects.
Imaging revealed a Dandy-Walker malformation and significant vascular abnormalities, increasing stroke risk.
Treatment included aspirin, propranolol, prednisolone, and topical timolol, resulting in clinical improvement.
Interpretation:
The case underscores the importance of recognizing large facial hemangiomas as potential indicators of PHACE syndrome, necessitating multidisciplinary evaluation and intervention.
Limitations:
The findings are based on a single patient, limiting generalizability.
Long-term outcomes and optimal imaging frequency for PHACE syndrome remain unclear.
Conclusion:
Early diagnosis and treatment of PHACE syndrome can lead to improved clinical outcomes and reduced risk of complications.
