PT - JOURNAL ARTICLE AU - Boulouis, G. AU - Dangouloff-Ros, V. AU - Boccara, O. AU - Garabedian, N. AU - Soupre, V. AU - Picard, A. AU - Couloigner, V. AU - Boddaert, N. AU - Naggara, O. AU - Brunelle, F. TI - Arterial Spin-Labeling to Discriminate Pediatric Cervicofacial Soft-Tissue Vascular Anomalies AID - 10.3174/ajnr.A5065 DP - 2017 Mar 01 TA - American Journal of Neuroradiology PG - 633--638 VI - 38 IP - 3 4099 - http://www.ajnr.org/content/38/3/633.short 4100 - http://www.ajnr.org/content/38/3/633.full SO - Am. J. Neuroradiol.2017 Mar 01; 38 AB - BACKGROUND AND PURPOSE: Differentiating major subtypes of cervicofacial vascular lesions is crucial for appropriate management. The aim of our study was to evaluate the performance of an MR imaging arterial spin-labeling perfusion sequence in discriminating pediatric cervicofacial soft-tissue vascular anomalies.MATERIALS AND METHODS: We conducted a retrospective analysis of data from a prospectively maintained registry including pediatric patients at a tertiary pediatric center between January 2012 and January 2014. We included pediatric patients with a final diagnosis of soft-tissue vascular anomalies and an MR imaging, including an arterial spin-labeling sequence at presentation. We performed an analysis of lesion perfusion, blinded to clinical data, by using concurrent spiral 3D pseudocontinuous arterial spin-labeling (1.5T magnet; spiral matrix, 512 × 8 mm; postlabeling delay, 1025 ms). Lesional flow was recorded with calibrated intralesional ROIs. Perfusion characteristics were compared among lesion subtypes with the Mood Median test.RESULTS: Among 840 patients screened, 46 matched the inclusion criteria and were included (median age, 1.45 years; interquartile range, 0.4–5.1 years; 27 females). Hemangiomas, including infantile hemangiomas (n = 18 patients) and noninvoluting (n = 2) and rapidly involuting (n = 1) congenital types, demonstrated marked hyperperfusion (median flow, 436 mL/min/100 g; interquartile range, 212.5–603 mL/min/100 g), significantly higher than that of lymphatic malformations (median, 22.5 mL/min/100 g; interquartile range, 16–60 mL/min/100 g; P < .001) or venous malformations (median, 25 mL/min/100 g; interquartile range, 15–66.5 mL/min/100 g; P = .003).CONCLUSIONS: MR imaging arterial spin-labeling is a valuable tool for the assessment of soft-tissue vascular anomaly hemodynamics and for the classification of major lesion subtypes.ASLarterial spin-labelingHIinfantile hemangiomaIQRinterquartile rangeNICHnoninvoluting congenital hemangiomaRICHrapidly involuting congenital hemangiomaSTVAsoft-tissue vascular anomaly