Colour Doppler ultrasound imaging findings in paediatric periocular and orbital haemangiomas

• Published in: Acta ophthalmologica (Oxford, England) Vol. 90; no. 8; pp. 727 - 732
• Main Authors: Spierer, Oriel, Neudorfer, Meira, Leibovitch, Igal, Stolovitch, Chaim, Kessler, Ada
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.12.2012; Wiley Subscription Services, Inc
• Subjects: Adrenergic beta-Antagonists - therapeutic use; Anesthesia; Blood Flow Velocity; capillary haemangioma; colour Doppler imaging; Eyelid Neoplasms - diagnostic imaging; Eyelid Neoplasms - physiopathology; Female; Follow-Up Studies; Glucocorticoids - therapeutic use; Hemangioma, Capillary - diagnostic imaging; Hemangioma, Capillary - drug therapy; Hemangioma, Capillary - physiopathology; Humans; Infant; Infant, Newborn; Male; Medical research; Neoplasm Regression, Spontaneous; Ophthalmology; Orbital Neoplasms - diagnostic imaging; Orbital Neoplasms - drug therapy; Orbital Neoplasms - physiopathology; paediatric orbital haemangioma; Propranolol - therapeutic use; Ultrasonography, Doppler, Color; ultrasound
• ISSN: 1755-375X; 1755-3768
• DOI: 10.1111/j.1755-3768.2011.02155.x

. Purpose:  To evaluate the combined grey‐scale ultrasonography (US) and colour Doppler imaging (CDI) as the first and primary imaging modalities in diagnosing paediatric orbital haemangiomas. Methods:  The charts of 20 consecutive children with a periorbital mass echographically diagnosed as a haemangioma between January 2004 and June 2009 in the Tel‐Aviv Sourasky Medical Center were reviewed. Data on demographic details, clinical findings, US and CDI characteristics, treatment and outcome were retrieved. Results:  Twelve (60%) haemangiomas were located on the upper eyelid, five in the lower eyelid (25%) and three in the medial cantus (15%). The tumour resolved completely in 10 children (50%) and in 10 children (50%) partial resolution was documented. Seven (35%) patients underwent treatment (intralesional or oral steroids or propranolol). Grey‐scale US depicted a solid‐tissue mass with low internal echogenicity. Mean haemangioma volume was 1.33 cm3. Colour Doppler imaging demonstrated intralesional flow with a mean peak systolic velocity of 15.2 cm per second and a mean resistance index of 0.51. All US and CDI examinations were carried out on alert children and no sedation or general anaesthesia was needed. During mean follow‐up time of 23 months, no child required any additional imaging or diagnostic procedures to confirm the diagnosis. Conclusion:  Combined US and CDI are suggested as the first imaging modalities in cases with a suspected diagnosis of periocular and orbital capillary haemangioma.